NONO directs PKM2-mediated H3T11ph to promote triple-negative breast cancer metastasis by activating SERPINE1 expression

NONO directs PKM2-mediated H3T11ph to promote triple-negative breast cancer metastasis by activating SERPINE1 expression | Research Square window.SnipcartSettings = { analytics: { enabled: false } }; (function() { var accessVector = localStorage.getItem('access_vector') || ''; window.dataLayer = window.dataLayer || []; if (accessVector) { window.dataLayer.push({ user: { profile: { profileInfo: { snid: accessVector } } } }); } })(); (function(w,d,s,l,i){w[l]=w[l]||[];w[l].push({'gtm.start':new Date().getTime(),event:'gtm.js'});var f=d.getElementsByTagName(s)[0],j=d.createElement(s),dl=l!='dataLayer'?'&l='+l:'';j.async=true;j.src='https://www.googletagmanager.com/gtm.js?id='+i+dl;f.parentNode.insertBefore(j,f);})(window,document,'script','dataLayer','GTM-K279D39R'); Browse Preprints In Review Journals COVID-19 Preprints AJE Video Bytes Research Tools Research Promotion AJE Professional Editing AJE Rubriq About Preprint Platform In Review Editorial Policies Our Team Advisory Board Help Center Sign In Submit a Preprint Cite Share Download PDF Research Article NONO directs PKM2-mediated H3T11ph to promote triple-negative breast cancer metastasis by activating SERPINE1 expression Qixiang Li, Hongfei Ci, Pengpeng Zhao, Dongjun Yang, Yi Zou, Panhai Chen, and 13 more This is a preprint; it has not been peer reviewed by a journal. https://doi.org/ 10.21203/rs.3.rs-5280141/v1 This work is licensed under a CC BY 4.0 License Status: Posted Version 1 posted You are reading this latest preprint version Abstract Background Emerging evidence has revealed that PKM2 has oncogenic functions independent of its canonical pyruvate kinase activity, serving as a protein kinase that regulates gene expression. However, the mechanism by which PKM2, as a histone kinase, regulates the transcription of genes involved in triple-negative breast cancer (TNBC) metastasis remains poorly understood. Methods We integrated cellular analysis, including cell viability, proliferation, colony formation, and migration assays; biochemical assays, including protein interaction studies and ChIP; clinical sample analysis; RNA-Seq and CUT&Tag data; and xenograft or mammary-specific gene knockout mouse models, to investigate the epigenetic modulation of TNBC metastasis via NONO-dependent interactions with nuclear PKM2. Results We report that the transcription factor NONO directly interacts with nuclear PKM2 and directs PKM2-mediated phosphorylation of histone H3 at threonine 11 (H3T11ph) to promote TNBC metastasis. We show that H3T11ph cooperates with TIP60-mediated acetylation of histone H3 at lysine 27 (H3K27ac) to activate SERPINE1 expression and to increase the proliferative, migratory, and invasive abilities of TNBC cells in a NONO-dependent manner. Conditional mammary loss of NONO or PKM2 markedly suppressed SERPINE1 expression and attenuated the malignant progression of spontaneous mammary tumors in mice. Importantly, elevated expression of NONO or PKM2 in TNBC patients is positively correlated with SERPINE1 expression, enhanced invasiveness, and poor clinical outcomes. Conclusion These findings revealed that the NONO-dependent interaction with nuclear PKM2 is key for the epigenetic modulation of TNBC metastasis, suggesting a novel intervention strategy for treating TNBC. Transcription Epigenomics H3T11ph NONO PKM2 Triple-negative breast cancer Metastasis Figures Figure 1 Figure 2 Figure 3 Figure 4 Figure 5 Figure 6 Figure 7 Background The latest international cancer survey report shows that there are approximately 20 million new cancer cases and 9.7 million cancer deaths worldwide in the year 2022, among which breast cancer ranks second for approximately 2.3 million new cases and fourth for approximately 0.67 million deaths [ 1 ]. Triple-negative breast cancer (TNBC) is a type of breast cancer that lacks the expression of estrogen receptor (ER), progesterone receptor (PR), and human epidermal growth factor receptor 2 (HER2) and has high malignancy, easy metastasis, and poor prognosis [ 2 ]. Currently, owing to the lack of specific and effective therapeutic targets, treatments for TNBC are limited, resulting in a shorter survival time for patients with TNBC. The mortality rate within five years of diagnosis for TNBC is as high as 40%, seriously threatening the physical and mental health of women [ 3 ]. Therefore, there is an urgent need to explore the pathogenesis and therapeutic strategies of TNBC. Transcriptional dysregulation has been recognized as a hallmark of cancer, where abnormal gene expression leads to tumor initiation and malignant progression [ 4 , 5 ]. The aberrant interplay between transcription factors and epigenetic regulators is key to cancer pathogenesis [ 6 ]. The multifunctional nuclear protein NONO (also known as P54nrb) was initially defined as a non-POU domain-containing octamer-binding protein belonging to the Drosophila behavior/human splicing (DBHS) family [ 7 , 8 ]. The protein structure of NONO contains RNA and DNA-binding domains, allowing it to participate in important biological processes such as precursor mRNA splicing, transcriptional regulation, nuclear retention of defective RNA, and DNA damage repair [ 9 ]. Our recent study revealed that the interaction between the transcription factors NONO and SOX6 synergistically silences γ-globin gene transcription in human erythroid cells [ 10 ]. The C-terminus of NONO has a nuclear localization sequence that assists in its distribution mainly in the nucleus and serves as an important component of paraspeckles [ 11 ]. However, NONO rarely functions alone and often interacts with other effector proteins to exert its biological effects [ 12 ]. In fact, as a binding protein of the TNBC subtype-specific and highly expressed membrane spike protein Moesin (MSN), NONO plays an important role in guiding the localization of MSN to nuclei and subsequent CREB phosphorylation activation to regulate TNBC progression [ 13 ]. Additionally, NONO can bind to EGFR in the nucleus to increase its stability and recruit CBP/P300 to enhance the transcriptional activity of EGFR, thereby enhancing nuclear EGFR-mediated tumorigenesis of TNBC [ 14 ]. NONO can also bind to IGFBP3 to activate PARP-dependent DNA damage repair, thereby increasing TNBC chemotherapy tolerance [ 15 ]. These studies clearly indicate that NONO is crucial for the development of TNBC. However, little is known about whether and how NONO, as a transcription factor, promotes malignant progression or metastasis of TNBC. Pyruvate kinase (PK), a rate-limiting enzyme in glycolysis, catalyzes the transfer of a phosphate group from phosphoenolpyruvate (PEP) to adenosine diphosphate (ADP) to yield pyruvate and ATP [ 16 ]. In the mammalian genome, the PKM1 and PKM2 isoforms are alternatively spliced products of the PKM gene by mutually exclusive use of exon 9 or exon 10, respectively. PKM1 is distributed in many normal differentiated tissues, whereas PKM2 is mainly expressed in most proliferating cells, including fetal and cancerous cells [ 17 , 18 ]. PKM2 has been characterized as a unique biomarker in cancer and has been shown to promote cancer cell proliferation and metastasis by driving the Warburg effect. However, its role in tumorigenesis in different cancers is controversial [ 17 , 18 ]. Importantly, in addition to its canonical metabolic enzyme function, PKM2 can translocate into the nucleus and function as a protein kinase and transcriptional co-activator [ 19 , 20 ]. PKM2 phosphorylates histone H3 at threonine 11 (H3T11ph), which is implicated in transcriptional activation [ 21 ]. However, the molecular mechanisms by which PKM2 is recruited to participate in gene transcriptional regulation and is precisely enriched across the genome within the nucleus are poorly understood. In this study, we found that NONO and PKM2 are important regulatory molecules involved in TNBC metastasis. We showed that NONO can specifically recruit PKM2 to coordinate the phosphorylation of threonine 11 of histone H3 (H3T11ph) and the acetylation of lysine 27 of histone H3 (H3K27ac), activating the transcription of multiple key genes, such as SERPINE1 (serine protease inhibitor family E member 1, encoding the PAI-1 protein) [ 22 , 23 ], thus promoting the migration and metastasis of TNBC cells. PAI-1 facilitates tumor cell detachment from the matrix and promotes tumor dissemination and metastasis and has been recommended as a promising biomarker for poor prognosis in primary breast cancer patients by the American Society of Clinical Oncology (ASCO) and the European Organization for Research and Treatment of Cancer (EORTC) clinical operation guidelines [ 22 , 23 ]. Our study revealed that NONO-dependent PKM2 coordinates histone H3 phosphorylation and acetylation to promote gene transcription and metastasis in TNBC cells. Methods Cell culture Human embryonic kidney (HEK293T) cells and two human TNBC cell lines (MDA-MB-231 and BT-549) were obtained from Shanghai Institute of Cell Biology, Chinese Academy of Sciences (Shanghai, China). MDA-MB-231 and HEK293T cells were cultured in Dulbecco’s modified Eagle’s medium (DMEM) (Gibco), and BT-549 cells were cultured in RPMI-1640 medium (Gibco) supplemented with 10% FBS (ExCell Bio) and 1% penicillin-streptomycin (100 U/ml, 100 µg/ml; Gibco). Cells were maintained at 37°C in a humidified incubator with 5% carbon dioxide. Cells were authenticated by short tandem repeat (STR) profiling and were negative for mycoplasma contamination. siRNA infection and shRNA lentiviral transduction The shRNA lentivirus was produced in HEK293T cells by co-transfection with PLKO.1-shRNA, the viral envelope plasmid pMD2. G, and the viral packaging plasmid psPAX2 using Lipofectamine 3000 (Invitrogen) following the manufacturer’s instructions. The scrambled (Scr) sequence was used as the negative control. At 48 h after infection, the viral supernatants were harvested and used to infect cells or stored at -80°C. To obtain stable cell lines, the cells were selected using 1 µg/mL puromycin (Yeasen, 60209ES100). The Scr and shRNA sequences used were as follows. Scr: 5’-CCTAAGGTTAAGTCGCCCTCG-3’ human NONO shRNA-1: 5’-CAGGCGAAGTCTTCATTCATA-3’ human NONO shRNA-2: 5’-TCCAGAGAAGCTGGTTATAAA-3’; human PKM2 shRNA-1: 5’-CTACCACTTGCAATTATTTGA-3’ human PKM2 shRNA-2: 5’-CCACTTGCAATTATTTGAGGA-3’ Negative control (NC) and specific siRNAs against NONO, PKM2, and TIP60 were synthesized by GenePharma (Suzhou, China). Cells were transiently transfected with 25 nM siRNA using the Lipofectamine 3000 transfection reagent. The siRNA sequences used were as follows: NC: 5’-UUCUCCGAACGUGUCACGU-3’ human NONO siRNA-1: 5’-CCUUACAGUUCGAAACCUU-3’; human NONO siRNA-2: 5’-GGAAGGCACUCAUUGAGAU-3’; human PKM2 siRNA-1: 5’-CCAUAAUCGUCCUCACCAA-3’ human PKM2 siRNA-2: 5’-GCCAUAAUCGUCCUCACCA-3’; human TIP60 siRNA-1: 5’-GGACAGCUCUGAUGGAAUA-3’; human TIP60 siRNA-2: 5’-GAUCGAGUUCAGCUAUGAA-3’; To overexpress PAI-1, human SERPINE1 cDNA was cloned and inserted into the lentiviral vector pLVX-IRES-mCherry at EcoRI and XbaI sites. Human KAT5 cDNA was cloned and inserted into the pcDNA3.1(+) vector at BamHI and XhoI sites for TIP60 overexpression. Cell proliferation, migration and invasion assays For the CCK-8 assay, cells were plated in 96-well plates at a concentration of 1.5 × 10 3 cells per well. After the addition of CCK-8 reagent (Vazyme Biotech, A311-01), the cells were incubated for 1.5 h at 37°C, after which absorbance at a wavelength of 450 nm was detected to construct a growth curve. For the colony formation assay, cells were seeded in 6-well plates at a density of 1 × 10 3 cells/well and cultured for 10 days. The cloned cells were fixed with 4% paraformaldehyde (PFA) for 30 min and stained with 0.1% crystal violet solution for 30 min. Finally, colonies were washed with distilled water, dried, and photographed. For cell migration assays, 3.5 × 10 4 cells were seeded on the chamber inserts of the Transwell apparatus (Corning, 3422) in serum-free medium, and medium supplemented with 10% FBS was added to the bottom chamber. After 12 h, the uninvaded cells on the upper surface of the Transwell chamber were removed using a moistened cotton swab. The migrated cells on the lower membrane surface were fixed with 4% PFA for 30 min and stained with a 0.1% crystal violet solution for 30 min. Imaging was performed using a fluorescence microscope at ×100 magnification, and images (six fields per membrane) were acquired using ImageJ software. The invasion assay was performed as described for the migration assay, except that the upper chamber was precoated with 50 µl of Matrigel solution. Western blot analysis Western blot analysis Total cell proteins were extracted using a cell lysis buffer (Beyotime, P0013) for western blotting and immunoprecipitation. Histone proteins were extracted using a standard protocol for acid extraction of histones from chromatin as previously reported [ 24 ]. Proteins were separated using 10% or 15% SDS-PAGE and transferred onto polyvinylidene difluoride (PVDF) membranes (Roche, Basel, Switzerland). The membranes were blocked for 1 h at room temperature in either 5% nonfat milk or BSA (Sigma) and then incubated with primary antibodies overnight at 4°C. After incubation with secondary antibodies, the protein bands were visualized using enhanced chemiluminescence (Tanon). All the primary antibodies used in this study are listed in Additional file 2: Table S4. Quantitative real-time PCR analysis (RT‒qPCR) Total RNA was prepared using TRIzol reagent (Invitrogen) according to the manufacturer’s instructions and assessed using a Nanodrop 2000 spectrophotometer (Thermo Fisher Scientific). Complementary DNAs (cDNAs) was produced using a HiScript II 1st Strand cDNA Synthesis Kit (Vazyme Biotech, R212-01). Quantitative real-time PCR analysis was performed using the AceQ qPCR SYBR Green Master Mix (Vazyme Biotech, R121-02) in a StepOnePlus RT‒PCR system (Thermo Fisher Scientific). GAPDH was used as a loading control. The primers used for qRT-PCR are listed in Additional file 2: Table S5. BioID2 pull-down and mass spectrometry analysis BioID2 pull-down experiments were performed as previously described with minor modifications [ 25 ]. Briefly, MDA-MB-231 cells transduced with the NONO-BioID2 fusion protein or BioID2-only control were seeded in 10-cm dishes. When the cells reached 80% confluence, the medium was replaced with complete medium containing 50 µM biotin (Sigma, B4501) and the cells were cultured for 16–18 h. The cells were subsequently lysed in lysis buffer (50 mM Tris HCl (pH 7.4), 500 mM NaCl, 0.2% SDS, 1 mM DTT, and 1× protease inhibitors), 0.1 µl of Pierce universal nuclease (Thermo Fisher Scientific, 88701) was added to each sample, and the mixture was incubated for 10 min at room temperature. After sonication and streptavidin affinity purification, the precipitates were washed with a wash buffer (8 M urea in 50 mM Tris, pH 7.4). Finally, the levels of biotinylated proteins were determined by mass spectrometry in collaboration with the BioProfile (Shanghai, China). GST pull-down assay The GST pull-down assay was performed as previously described [ 26 ]. Briefly, the pGEX-6P-1 plasmid encoding GST, full-length GST-NONO and fragments, full-length GST-PKM2, fragments, and mutants, as well as the pET28a plasmid encoding His-NONO and His-PKM2, were expressed in E. coli BL21 and purified using glutathione S-transferase beads (GenScript, L00206) or nickel-nitrilotriacetic acid beads (GenScript, L00206) according to standard protocols. The His-PKM2 protein was mixed with purified GST, full-length GST-NONO, or fragments for 4 h at 4°C. Similarly, His-NONO proteins were incubated with GST, GST-PKM2 full-length or fragments or mutants at 4°C for 4 h. The beads were washed five times, and the results were analyzed by western blotting. Immunofluorescence staining The cells were cultured overnight on glass coverslips, fixed with 4% PFA for 20 min, and permeabilized with 0.2% Triton X-100 for 20 min. After blocking with 5% BSA for 30 min, cells were incubated with primary antibodies against NONO (HUABIO, ET7108-81) and PKM2 (Proteintech, 60268-1-lg) overnight at 4°C, followed by incubation with fluorescence-conjugated secondary antibodies for 1 h at room temperature. The cells were then gently washed with PBS and the nuclei were stained with DAPI for 5 min at room temperature. Images were acquired using a confocal laser scanning microscope (Olympus). RNA-seq and data analysis Total RNA was isolated from the NC, NONO-knockdown, and PKM2-knockdown MDA-MB-231 cells. RNA purification, reverse transcription, library construction, and sequencing were performed in collaboration with Majorbio Biotechnology (Shanghai, China) according to the manufacturer’s instructions (Illumina, San Diego, CA, USA). To identify differentially expressed genes (DEGs), gene expression was calculated as transcripts per million reads (TPM). A fold change > 2.0, and a P value < 0.05 were used as the cutoff values and were considered to indicate significantly differentially expressed genes. Chromatin immunoprecipitation (ChIP) assay ChIP assays were performed using MDA-MB-231 cells in accordance with previously described methods [ 26 ]. Normal rabbit IgG (ab172730; Abcam) was used as the control. ChIP DNAs was analyzed by quantitative PCR using Rotor-Gene 6000 (Corbett Research). Primer sequences used for ChIP are listed in Additional file 2: Table S6. CUT&Tag CUT&Tag was processed according to a previously reported protocol [ 27 ]. This experiment was performed in MDA-MB-231 cells, and antibodies against NONO (Abcam, ab70335), H3T11ph (Active motif, 39151), and H3K27ac (Abcam, ab4729) were used in this study. DNA libraries were sequenced on an Illumina NovaSeq 6000 platform (DIATRE Biotechnology, Shanghai, China). Tissue microarrays and IHC staining Human TNBC tissue microarrays (no. TNBC1202), and clinicopathological data were obtained from Shanghai Superbiotek (Shanghai, China). IHC staining was performed according to the standard protocol of the Cell Signaling Technology. Tissue slides were incubated with primary antibodies specific for NONO (HUABIO, ET7108-81), PKM2 (Proteintech, 15822-1-AP), PAI-1 (Abcam, ab125687), and Ki-67 (Abcam, ab15580), followed by incubation with horseradish peroxidase (HRP)-conjugated secondary antibodies. The staining of NONO, PKM2, and PAI-1 in human TNBC tissues was independently assessed using a semi-quantitative H-score system by two experienced pathologists blinded to the clinical data [ 28 ]. Animal studies Mice were maintained in a specific pathogen-free (SPF) facility on a 12 h light/dark cycle at a controlled temperature (20–23°C) and humidity (45–65%). The sample size was chosen with adequate power based on the literature and our previous experience [ 28 ]. For each experiment, it is indicated in the figure legend. Prior to the experiment, the mice were randomly assigned to different treatment groups. MMTV-PyMT mice on the FVB background were purchased from GemPharmatech (Nanjing, China). For NONO or PKM2 knockdown in MMTV-PyMT (FVB) mice, pAAV-U6-EGFP plasmids were transformed with shRNAs and AAVs were obtained from Syngentech (Beijing, China). AAVs were intraductally injected into the mammary glands of 5-week-old female MMTV-PyMT (FVB) mice as previously described [ 29 ]. After 2 weeks, tumor size was determined once a week, and tumor volumes were calculated using the following formula: volume (mm 3 ) = 1/2 × length × width 2 . All mice were euthanized at 12 weeks of age, and tumor and lung samples were collected, weighed, photographed, and stained with H&E. The Scr sequence was used as the negative control. The shRNA sequences used were as follows: Scr: 5’-CCTAAGGTTAAGTCGCCCTCGC-3’ Mouse NONO shRNA-1: 5’-GCTGCAACAATGGAAGGAATT-3’ Mouse NONO shRNA-2: 5’-ACACGAACCCTAGCGGAAATT-3’ Mouse PKM2 shRNA-1: 5’-CTACCACTTGCAGCTATTCGA-3’ Mouse PKM2 shRNA-1: 5’-CCACTTGCAGCTATTCGAGGA-3’ For xenograft models, 6-week-old female BALB/c nude mice were purchased from GemPharmatech (Nanjing, China). MDA-MB-231 cells were infected individually with Scr, NONO-KD, or NONO-KD + PAI-1 lentivirus to establish stable cell lines. Subsequently, each mouse was injected subcutaneously with 5 × 10 6 cells (suspended in 100 µl of PBS with 100 µl of Matrigel). Tumor size was measured every 3 days with a caliper, and the average tumor volume reached 100 mm 3 . After 21 days, all nude mice were sacrificed, and subcutaneous tumors were harvested, weighed, and photographed. To establish mammary-specific NONO or PKM2 knockout models in spontaneous mammary tumor mice, MMTV-Cre and NONO-floxed mice on a C57BL/6 strain background were obtained from GemPharmatech (Nanjing, China). MMTV-PyMT mice and PKM2-floxed mice on a C57BL/6 background were purchased from Jackson Laboratory (New York, USA). To obtain NONO knockout (MMTV-Cre +/− ::MMTV-PyMT + ::NONO fl/fl ) female mice, MMTV-Cre +/− ::NONO fl/fl female mice were crossed with the male MMTV-PyMT + ::NONO fl/Y mice. Female littermates (MMTV-Cre −/− ::MMTV-PyMT + ::NONO fl/fl ) were used as controls. Similarly, to obtain PKM2 knockout (MMTV-Cre +/− ::MMTV-PyMT + ::PKM2 fl/fl ) female mice, MMTV-Cre +/− ::PKM2 fl/fl female mice were crossed with MMTV-PyMT + ::PKM2 fl/fl male mice. Female littermates (MMTV-Cre −/− ::MMTV-PyMT + ::PKM2 fl/fl ) were used as controls. The overall tumor burden was measured once a week using a digital caliper beginning at week 16, and the mice were humanely euthanized at 24 weeks of age. Mammary tumors were harvested for histology, flash-frozen for protein and RNA isolation, and subjected to IHC staining with the indicated antibodies, whereas the lungs were extracted for H&E staining. A blinding strategy was used whenever possible when assessing outcomes. The sequences of the PCR primers used for genotyping transgenic mice are listed in Additional file 2: Table S7. Statistical analysis All data are presented as mean ± SD unless otherwise indicated. GraphPad Prism software (version 7.0) was used to assess significant differences between groups. Comparisons between two groups were performed using an unpaired two-tailed Student’s t-test. Multiple comparisons were performed using a one-way analysis of variance (ANOVA). P < 0.05. One, two, three, and four asterisks indicate P < 0.05, P < 0.01, P < 0.001, and P < 0.0001, respectively. Results NONO directly interacts with nuclear PKM2 in TNBC cells The paraspeckle protein NONO plays a critical role in TNBC, although its direct downstream transcriptional target genes are unknown [ 13 – 15 ]. To identify potential proteins that interact with NONO, we used a proximity-dependent biotinylation identification approach known as BioID2 [ 25 ], in which NONO is fused to the N-terminus of the BioID2 vector and transduced into human MDA-MB-231 cells. An empty vector containing only BirA biotin ligase was used as the control. After biotin-streptavidin affinity purification, proteins associated with NONO were analyzed using quantitative mass spectrometry. Among the proteins that were specifically enriched in NONO-BioID2-expressing cells, PKM2 was identified as an NONO-interacting protein in the top 10 list (Fig. 1 A, Additional file 2: Table S1 ). In addition, we found that SFPQ, PSPC1, and MSN [ 12 – 14 ], which are NONO-binding proteins, are also present. To confirm the interaction between NONO and PKM2, we performed co-immunoprecipitation (co-IP) experiments and found that NONO interacted with PKM2 in both MDA-MB-231 and BT-549 cells (Fig. 1 B and C). Furthermore, immunofluorescence staining revealed that NONO co-localized with PKM2 in the nuclei of MDA-MB-231 cells (Fig. 1 D). These results agree with previous observations that PKM2 is present in the nucleus [ 20 , 21 , 30 ]. Next, we found that NONO directly interacted with PKM2 in the GST pull-down experiments (Fig. 1 E). To further characterize the determinants mediating the association between NONO and PKM2, we mapped NONO protein domains using GST pull-down experiments and demonstrated that the NOPS and coiled-coil domains of NONO were sufficient for their interaction (Fig. 1 F). Similarly, we demonstrated that the A and C domains of PKM2 were responsible for its interaction with NONO (Fig. 1 G), indicating that NONO interacts with PKM2 through multiple domains. Taken together, these data indicate that PKM2 is a novel protein that interacts with NONO in the TNBC cell nuclei. NONO expression is associated with the prognosis of TNBC patients, and NONO is required for TNBC cell metastasis To investigate the clinical significance of NONO expression in patients with TNBC, we first analyzed NONO expression by immunohistochemistry (IHC) using tissue microarrays containing 60 TNBC samples and matched adjacent normal tissues. We observed that NONO expression was significantly upregulated in TNBC tissues compared to that in the adjacent normal tissues (Fig. 2 A and B). Notably, NONO expression correlated with tumor size and higher-grade lymph node status in patients with TNBC (Fig. 2 C; Additional file 2: Table S2). Importantly, Kaplan-Meier survival analysis revealed that TNBC patients with high NONO expression had a shorter overall survival (Fig. 2 D). The expression levels of NONO in TNBC tissues were significantly higher than those in non-TNBC tissues (Additional file 1: Fig. S1 A). These results indicate that NONO is upregulated in human TNBC tissues and correlates with poor prognosis in patients with TNBC, suggesting that NONO may promote cancer cell invasion during malignant progression. To determine the effect of NONO on cell growth and invasion, two independent short hairpin RNAs (shRNAs) targeting NONO were used to silence NONO expression. The knockdown efficiency of NONO in human MDA-MB-231 and BT-549 TNBC cell lines was determined by western blot analysis (Fig. 2 E). CCK-8 and colony formation assays indicated that the proliferation of MDA-MB-231 and BT-549 cells was significantly inhibited upon NONO knockdown compared with that of scrambled control (Scr) cells (Fig. 2 F and G). Transwell assays revealed that the migratory and invasive abilities of TNBC cells were significantly lower in the NONO knockdown group than in the Scr group (Fig. 2 H). In addition, the well-established MMTV-PyMT (FVB background) transgenic murine model of spontaneous mammary tumors [ 31 ] was used to determine whether NONO directly regulated tumorigenesis. Remarkably, adeno-associated virus (AAV)-mediated NONO depletion in mouse breast tissue was sufficient to attenuate tumor growth (Fig. 2 I, J, and K). More importantly, NONO depletion substantially reduced the number of metastatic lung nodules (Fig. 2 L and M). These results indicated that NONO is crucial for TNBC growth and metastasis. PKM2 expression is upregulated in TNBC, and knockdown of PKM2 inhibits TNBC cell metastasis Similarly, we investigated the clinical significance of PKM2 expression in TNBC patients and found that PKM2 expression was upregulated in human TNBC tissues and correlated with poor prognosis in TNBC patients (Fig. 3 A, B, and C; Additional file 1: Fig. S1 B and Table S3), which is consistent with previous results [ 30 ] and further suggests that PKM2 may promote cancer cell invasion during malignant progression. Furthermore, our in vitro knockdown experiments (Fig. 3 D, E, F, and G) and in vivo animal study results (Fig. 3 H, I, J, K, and L) indicated that PKM2 is crucial for TNBC growth and metastasis. SERPINE1 is a key transcriptional target of NONO and PKM2 in TNBC cells Next, we sought to understand how NONO and PKM2 regulate the migration and invasion of TNBC cells. To identify potential transcriptional targets of the NONO/PKM2 complex, we performed RNA-seq analysis to profile co-regulated target genes. Through integrated analysis of RNA-seq results following NONO and PKM2 knockdown in MDA-MB-231 cells, we found that nearly half of the differentially expressed genes DEGs (451/999) following NONO knockdown were also regulated by PKM2 (Fig. 4 A, GSE266177). Further analysis revealed that SERPINE1 (encoding the PAI-1 protein) [ 22 , 23 , 32 ] was the gene whose expression was most downregulated by either NONO or PKM2 knockdown (Fig. 4 B, GSE266177). In the top 10 heatmaps, IL11, CCN2, RCN1, VDAC1, CDKN1A (P21), ADAMTSL4, MATN2, FERMT2, and MCAM, which play key roles in cell growth, adhesion, migration, and differentiation [ 33 – 40 ], were significantly downregulated when either NONO or PKM2 was knocked down. Given that PAI-1 facilitates tumor cell detachment from the matrix and promotes tumor dissemination and metastasis, which has been recommended as a promising biomarker for poor prognosis in primary breast cancer patients by the American Society of Clinical Oncology (ASCO) and the European Organization for Research and Treatment of Cancer (EORTC) clinical operation guidelines [ 22 , 23 ], we selected SERPINE1 as a primary target for further study. We confirmed that NONO knockdown in MDA-MB-231 cells significantly reduced the expression of SERPINE1 at both the transcriptional and protein level (Fig. 4 C and D). Subsequently, we examined whether the enforced expression of PAI-1 would compensate for NONO knockdown. We first overexpressed exogenous PAI-1 in NONO-depleted MAD-MB-231 cells (Fig. 4 E). We then performed CCK-8, colony formation, and Transwell assays using these cells. We found that the overexpression of PAI-1 significantly rescued the reduced proliferation, migration, and invasion of NONO-depleted cells (Fig. 4 F, G, and H). To further support the in vitro results, we performed in vivo analysis using xenograft models in nude mice. We showed that overexpression of PAI-1 significantly reversed the growth defects in NONO-depleted MDA-MB-231 xenograft tumors (Fig. 4 I, J, and K). Similarly, we found that knockdown of PKM2 significantly reduced SERPINE1 transcription in MDA-MB-231 cells (Fig. 4 L and M). The proliferative, migratory, and invasive capabilities of PKM2-depleted MDA-MB-231 cells could be rescued by ectopic expression of PAI-1 (Fig. 4 N, O, P, and Q). Consistent experimental results were obtained regarding the roles of NONO and PKM2 in human BT-549 TNBC cells (Additional file 1: Fig. S2A-L). To further investigate the clinical relevance of PAI-1 expression in patients with TNBC, we examined its expression using IHC on tissue microarrays containing 60 pairs of TNBC samples and their matched adjacent normal tissues. We demonstrated that PAI-1 was notably upregulated in TNBC tissues compared to adjacent normal tissues (Additional file 1: Fig. S2M and N). Importantly, the expression levels of NONO and PAI-1, as well as those of PKM2 and PAI-1, were significantly positively correlated in human TNBC samples according to Pearson correlation analysis (Fig. 4 R), further confirming that SERPINE1 is the downstream target gene of NONO/PKM2 in TNBC cells. Collectively, these data suggest that NONO/PKM2 promotes TNBC progression by activating SERPINE1 transcription. NONO-dependent PKM2 and its nuclear protein kinase activity are critical for SERPINE1 transcription and TNBC progression Given that NONO and PKM2 positively regulate SERPINE1 transcription in TNBC cells, and that they directly interact in the nucleus, we investigated how they regulate SERPINE1 expression. As expected, enforced the overexpression of PKM2 enhanced SERPINE1 expression. However, this increase in expression was abolished by NONO knockdown (Fig. 5 A and B). Next, we examined whether PKM2-mediated H3T11ph modifications at the SERPINE1 promoter were enriched in a NONO-dependent manner. ChIP‒qPCR revealed a significant reduction in H3T11ph enrichment at the SERPINE1 promoter in the NONO knockdown group compared to that in the negative control (NC) group (Fig. 5 C). Previous studies have demonstrated that PKM2 exhibits pyruvate kinase or protein kinase activity, which depends on its cytosolic tetramer or nuclear dimer state [ 19 , 41 , 42 ]. To further explore whether the protein kinase of PKM2 is crucial for SERPINE1 transcriptional activation, we utilized two well-established PKM2 mutants, PKM2-Y105F (predominant tetramer form harboring pyruvate kinase activity) [ 42 ] and PKM2-R399E (predominant dimer form harboring protein kinase activity) [ 19 ] to examine their effects on SERPINE1 expression. We overexpressed PKM2-WT, PKM2-Y105F, or PKM2-R399E in PKM2-depleted MDA-MB-231 cells. We found that the PKM2-Y105F mutant did not activate SERPINE1 expression, whereas the PKM2-R399E mutant had an activating effect on SERPINE1 expression similar to that of PKM2-WT (Fig. 6 D and E). These results suggest that the protein kinase activity of PKM2 is key to activating SERPINE1 expression in the nucleus. To identify the potential key residues of PKM2 responsible for NONO interactions, we used the ZDOCK server ( https://zdock.umassmed.edu/ ) for molecular docking analyses. Molecular docking confirmed good and stable binding of NONO to PKM2 (Additional file 1: Fig. S3A) and revealed seven positions of PKM2 that may play important roles in the interaction between PKM2 and NONO (Additional file 1: Fig. S3B). GST pull-down assays demonstrated that the PKM2-S406A mutant (Ser to Ala at aa 406) significantly reduced this interaction, whereas the interactions of PKM2-R400A, T412A, D476A, D487A, W515A, and R526A mutants with NONO were similar to those of wild-type PKM2 (PKM2-WT, Fig. 5 F). To explore the effect of the S406A mutation of PKM2 on TNBC progression, we overexpressed PKM2-WT or the PKM2-S406A mutant in MDA-MB-231 cells. Consistently, the PKM2-S406A mutant immunoprecipitated significantly less NONO in the MDA-MB-231 cells (Fig. 5 G). Notably, the PKM2-S406A mutant exhibited the same subcellular distribution as that of PKM2-WT (Fig. 5 H). However, compared with PKM2-WT, PKM2-S406A overexpression in MDA-MB-231 cells failed to activate SERPINE1 expression (Fig. 5 I and J). In addition, we found that compared to PKM2-WT, PKM2-S406A overexpression in MDA-MB-231 cells significantly inhibited cell growth, migration, and invasion (Fig. 5 K, L, and M). Taken together, these results demonstrated that NONO-dependent PKM2 and its nuclear protein kinase activity are crucial for SERPINE1 expression and TNBC cell invasion. PKM2-mediated H3T11ph cooperates with TIP60-mediated H3K27ac to promote SERPINE1 expression A previous study has revealed that PKM2 mediates H3T11ph, which is involved in transcriptional regulation [ 21 ]. To explore the effect of PKM2 on other histone modifications, we examined global changes in other key histone H3 modifications upon PKM2 knockdown in MDA-MB-231 cells. As expected, the levels of H3T11ph were markedly decreased upon PKM2 knockdown (Fig. 6 A). Interestingly, we found that the levels of H3K27ac, a promoter and enhancer marker [ 43 – 45 ], were markedly lower in PKM2-knockdown cells than in NC cells (Fig. 6 A). Additionally, we observed that the levels of the histone markers H3K4me1 and H3K9ac, which have been previously described [ 21 ], decreased upon PKM2 knockdown (Fig. 6 A). There were no obvious changes in the levels of H3T3ph, H3K4me2/3, H3K4ac, H3K9me3, H3S10ph, H3K14ac, H3K14la, H3R17me2s, H3K18ac, or H3K27me2/3 modifications between PKM2 knockdown cells and NC cells (Fig. 6 A). These data suggested that PKM2-mediated H3T11ph cooperates with H3K27ac to regulate gene transcription in TNBC cells. To understand how NONO, H3T11ph, and H3K27ac collaborate to regulate gene transcription, we performed cleavage under targets and tagmentation (CUT&Tag) experiments in MDA-MB-231 cells to determine the enrichment profiles of NONO, H3T11ph, and H3K27ac in the whole genome. Interestingly, we found that NONO, H3T11ph, and H3K27ac signals were significantly enriched at transcription start sites (TSSs), implying that they may perform transcriptional regulatory functions (Fig. 6 B, GSE266179). In addition, H3T11ph and H3K27ac signals were markedly reduced in PKM2-KD cells compared to their respective NC cells (Fig. 6 B), which was in good agreement with our western blot analysis results (Fig. 6 A). In fact, we found that NONO, H3T11ph, and H3K27ac were co-enriched in the promoter, TSS, and 3’-end regions of SERPINE1 (Fig. 6 C). These results were further confirmed by ChIP‒qPCR in MDA-MB-231 cells (Fig. 6 D). Notably, NONO enrichment largely overlapped with H3T11ph peaks genome-wide in MDA-MB-231 cells (Additional file 1: Fig. S4A, GSE266179). Moreover, through bioinformatics analysis, we found that the genome-wide occupancy of NONO and H3T11ph, H3T11ph, and H3K27ac was highly correlated, although there was no significant correlation between NONO and H3K27ac (Additional file 1: Fig. S4B). These results further suggest that PKM2-mediated H3T11ph could be enriched in promoters through NONO recruitment of PKM2, where H3T11ph cooperates with H3K27ac to activate SERPINE1 transcription. Next, we explored the possible link between H3T11ph and H3K27ac. We searched the RNA-seq data obtained upon PKM2 knockdown (GSE266177) and examined changes in the expression levels of histone acetyltransferases KAT5 (encoding TIP60), KAT3B (encoding PCAF), CREBBP (encoding CBP), and EP300 (encoding P300), which are associated with histone acetylation. We then performed western blot analyses and found that PKM2 knockdown significantly reduced the expression of TIP60 but upregulated P300 expression in MDA-MB-231 cells, whereas the expression of PCAF and CBP remained unchanged compared with that in NC controls (Additional file 1: Fig. S5A). Therefore, we selected KAT5/TIP60 for further study. RT-qPCR assays confirmed that KAT5 mRNA levels significantly decreased following PKM2 knockdown (Additional file 1: Fig. S5B). Similar results were obtained for the BT-549 cells (Additional file 1: Fig. S6A and B). In addition, our CUT&Tag data demonstrated that H3T11ph modifications were enriched in the KAT5 promoter and that H3T11ph enrichment was significantly reduced in the promoter upon PKM2 knockdown (Additional file 1: Fig. S5C). Consistent results were obtained by ChIP‒qPCR in MDA-MB-231 cells (Additional file 1: Fig. S5D). These data indicated that PKM2 directly activates KAT5 transcription. To determine whether TIP60 regulates SERPINE1 expression, we knocked down KAT5 expression in MDA-MB-231 cells. KAT5 knockdown significantly reduced SERPINE1 expression in MDA-MB-231 cells compared to that in NC control cells (Additional file 1: Fig. S5E and F). As expected, the levels of H3K27ac were markedly reduced following KAT5 knockdown (Additional file 1: Fig. S5F). Importantly, the levels of PAI-1 and H3K27ac in PKM2-depleted MDA-MB-231 cells were partially restored by ectopic TIP60 expression (Additional file 1: Fig. S5G). These results were also observed in BT-549 cells (Additional file 1: Fig. S6C, D and E). In addition, we analyzed the expression profiles extracted from GEO datasets (GSE76275) and found that the expression of PKM2 and KAT5 was positively correlated in human TNBC samples (Additional file 1: Fig. S6F). Taken together, these results suggest that PKM2 can also transcriptionally regulate KAT5 expression and that TIP60-mediated H3K27ac cooperates with PKM2-mediated H3T11ph to activate SERPINE1 expression. NONO or PKM2 deficiency reduces PAI-1 expression and inhibits the malignant progression of spontaneous mammary tumors in mice The nuclear protein NONO is highly conserved in humans and mice, and shares 98% amino acid sequence similarity [ 7 , 8 ]. To further assess the role of NONO in regulating mammary tumor progression in vivo , we constructed a spontaneous mammary tumor mouse line in which NONO was specifically knocked out in the breast tissue (Fig. 7 A). Consistent with our previous results, conditional loss of NONO in mammary tissue significantly inhibited tumor growth (Fig. 7 B and C; Additional file 1: Fig. S7A). In addition, knockout of NONO markedly reduced the lung metastatic capacity and suppressed the formation of larger metastatic nodules in spontaneous mammary tumor model mice (Fig. 7 D). The intratumoral levels of NONO, PAI-1, and Ki67 were analyzed using western blotting and immunohistochemical (IHC) staining. Conditional mammary NONO depletion significantly reduced PAI-1 and Ki67 expression (Fig. 7 E and F; Additional file 1: Fig. S7B). We also generated a mouse model of spontaneous breast cancer with mammary-specific PKM2 knockout (Fig. 7 G). Similarly, tumor growth and lung metastatic capacity were significantly inhibited by conditional PKM2 knockout in breast tissue (Fig. 7 H, I, and J; Additional file 1: Fig. S7C). The intratumoral levels of PKM2, PAI-1, and Ki67 were analyzed using western blotting and immunohistochemical (IHC) staining. Conditional mammary PKM2 depletion significantly reduced PAI-1 and Ki67 expression (Fig. 7 K and L; Additional file 1: Fig. S7D). Taken together, these in vivo data reinforce the notion that NONO and PKM2 are critical for the malignant progression of breast tumors via SERPINE1 transcriptional activation. Discussion The prognosis of patients with TNBC remains poor because of the lack of specific biomarkers for effective interventions [ 2 , 46 ]. Therefore, elucidating novel molecular mechanisms and developing effective therapeutic targets for TNBC is highly important. In this study, we found that NONO specifically interacts with nuclear PKM2 to transcriptionally activate SERPINE1 expression and promote TNBC cell metastasis. In addition, we found that PKM2-mediated H3T11ph cooperates with TIP60-mediated H3K27ac to regulate gene transcription in an NONO-dependent manner. These results revealed a novel mechanism by which PKM2, a protein kinase, directly regulates gene transcription and promotes TNBC metastasis. As a multifunctional nuclear protein, NONO has diverse functions in tumorigenesis, through which it may interact with distinct protein partners [ 12 ]. Previous studies have shown that NONO interacts with the Hippo pathway effector TAZ to undergo liquid–liquid phase separation, which promotes TAZ-mediated oncogenic transcription [ 47 ]. In addition, a recent study demonstrated that NONO is important for transactivation of EGFR by stabilizing nuclear EGFR expression and recruiting other transcriptional coactivators [ 14 ]. However, how the NONO-driven transcriptional program facilitates malignant development of cancer remains unclear. In this study, we found that PKM2 directly interacted with NONO and executed its protein kinase function to facilitate TNBC metastasis. Our data showed that NONO enrichment was strongly correlated with nuclear PKM2-mediated H3T11ph marks along genomic loci, including SERPINE1 . Interestingly, we observed that approximately 45% of the NONO-targeting genes were also regulated by PKM2 in TNBC cells. These findings suggested that nuclear PKM2 is important for NONO-mediated gene expression in TNBC cells. In addition to its glycolytic function, PKM2 has non-metabolic functions that are critical for gene expression. Within the nucleus, PKM2 is a transcriptional coactivator that confers malignant potential to cancer cells through its association with various transcription factors including Oct-4, HIF-1α, β-catenin, and STAT3 [ 19 , 20 , 48 , 49 ]. However, the regulatory processes associated with non-metabolic PKM2 involve non-histone phosphorylation (H3T11ph)-mediated transcription of downstream target genes. Intriguingly, upon EGF receptor activation, PKM2 binds histone H3 and phosphorylates histone H3 at T11, resulting in the acetylation of histone H3 at K9 to activate CCND1 and MYC expression in glioblastoma cells [ 21 ]. In addition, a recent study reported that PKM2 interacts with the histone methyltransferase EZH2 to regulate the metabolic switch from glycolysis to fatty acid βoxidation in TNBC [ 30 ]. However, there was no indication of how PKM2/EZH2 was recruited to the target genes in this study [ 30 ]. In contrast, we did not observe any change in H3K27me3 levels upon PKM2 knockdown compared with the NC control in MDA-MB-231 cells in our study. This discrepancy could be due to different cell sources and manipulations. Interestingly, in the current study, we found that PKM2 phosphorylated histone H3 at T11 in a NONO-dependent manner, and this phosphorylation coincided with the acetylation of histone H3 at K27 to activate SERPINE1 expression in TNBC. These results revealed more precise genome-wide enrichment of PKM2-mediated H3T11ph and demonstrated a novel crosslink between histone marks. H3K27ac is an active enhancer mark [ 43 – 45 ]. Thus, our data suggests that PKM2-mediated H3T11ph may also be associated with active enhancers. NONO can bind to enhancer regions in human glioblastoma cells and mouse retina [ 47 , 50 ]. Therefore, the mechanism by which PKM2-mediated H3T11ph modification is linked to the NONO-mediated regulation of enhancer activity warrants further investigation. Nevertheless, the specific role of PKM2 makes it an attractive therapeutic target in cancer treatment. However, the complexity of PKM2 regulation and signaling has led researchers to face the following dilemma: whether to use PKM2 activators or inhibitors for cancer treatment [ 17 ]. The current study provides an alternative intervention strategy for treating TNBC by inhibiting or interfering with the interaction between NONO and PKM2. PAI-1 is a major member of the serine protease inhibitor (serpin) superfamily and functions as an inhibitor of tissue-type plasminogen activator (tPA) and urokinase-type plasminogen activator (uPA) [ 51 ]. tPA/uPA is mainly involved in the conversion of plasminogen to active plasmin, leading to fibrin clot hydrolysis [ 51 ]. Therefore, PAI-1 plays an important role in various vascular disorders such as thrombosis, atherosclerosis, and myocardial infarction [ 52 ]. Interestingly, accumulating evidence has demonstrated that PAI-1 plays a pro-tumorigenic role in cancer, although it was originally hypothesized to have antitumor effects [ 53 ]. Owing to the strong correlation between PAI-1 levels and prognosis in patients with breast cancer, PAI-1 has been recommended as a biomarker for therapeutic decisions in patients with clinically node-negative breast cancer [ 54 ]. Several studies have shown that PAI-1 is critical for TNBC cell growth and metastasis [ 32 , 55 , 56 ]. In the present study, we demonstrated that NONO can recruit nuclear PKM2, which triggers the phosphorylation of histone H3 at T11 to directly activate SERPINE1 expression and mediate cell proliferation, migration, and invasion in TNBC cells. More importantly, NONO and PKM2 expression strongly correlated with the expression of PAI-1 in TNBC tissues. These findings identified a novel transcriptional regulatory pathway for SERPINE1 expression and support the function of the NONO-PKM2 interaction in the malignant progression of TNBC. Conclusion Taken together, our findings demonstrate that NONO interacts with nuclear PKM2 and directs histone H3 phosphorylation to promote tumor metastasis, highlighting the potential of disrupting the association between NONO and PKM2 for the targeted therapy of malignant TNBC. Abbreviations NONO Non-POU domain-containing octamer-binding protein PKM2 Pyruvate kinase isozyme type M2 H3T11ph Phosphorylation of histone H3 at threonine 11 H3K27ac Acetylation of histone H3 at lysine 27 SERPINE1 Serine protease inhibitor family E member 1 PAI-1 Plasminogen Activator Inhibitor 1 TNBC Triple-negative breast cancer ChIP Chromatin immunoprecipitation CUT&Tag Cleavage under targets and tagmentation TSS transcription start sites IHC immunohistochemical staining. DEG:Differentially expressed genes. TIP60:HIV-tat interacting protein 60kD. Declarations Acknowledgments We thank the members of the Zhao Laboratory for their helpful discussions. Authors’ contributions Q.L., H.C., P.Z., D.Y., Y.Z., P.C., D.W., W.S., W.L., X.M., M.X., and Y.C. performed biochemical experiments and bioinformatics analysis. Q.L., H.C., P.Z., Y.C., B.C., and Z.J. performed animal experiments and provided pathology expertise. M.Z., L.K., K.Z., and D.C.S.H. provided critical reagents and expertise. Q.L., Z.J. and Q.Z. designed the project and wrote the manuscript. Funding This work was supported by the National Natural Science Foundation of China (NSFC #32270619 and #31970615), Fundamental Research Fund of the State Key Laboratory of Pharmaceutical Biotechnology (#LNSN-202403), Key Project of Natural Science Research for the University of Anhui Province (No. 2023AH051989), and Natural Science Foundation of Bengbu Medical College (2021byzd141, 2023bypy013). Availability of data and materials All relevant data are available within the article and additional files or from the authors upon request. Raw mass spectrometry proteomics data were deposited in the ProteomeXchange consortium under the accession number PXD051842. The RNA-Seq and CUT&Tag data generated for this study were deposited in the Gene Expression Omnibus (GSE266177, GSE266179). 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Also discoverable on Platform About Our Team In Review Editorial Policies Advisory Board Help Center Resources Author Services Accessibility API Access RSS feed Manage Cookie Preferences © Research Square 2026 | ISSN 2693-5015 (online) Privacy Policy Terms of Service Do Not Sell My Personal Information {"props":{"pageProps":{"initialData":{"identity":"rs-5280141","acceptedTermsAndConditions":true,"allowDirectSubmit":true,"archivedVersions":[],"articleType":"Research Article","associatedPublications":[],"authors":[{"id":369119701,"identity":"bf7cc557-d2c4-4c5d-9002-4c4d642d19fc","order_by":0,"name":"Qixiang Li","email":"","orcid":"","institution":"Nanjing University","correspondingAuthor":false,"prefix":"","firstName":"Qixiang","middleName":"","lastName":"Li","suffix":""},{"id":369119702,"identity":"23597a21-0044-40c5-ba53-2c248596abf1","order_by":1,"name":"Hongfei Ci","email":"","orcid":"","institution":"The First Affiliated Hospital of Bengbu Medical University","correspondingAuthor":false,"prefix":"","firstName":"Hongfei","middleName":"","lastName":"Ci","suffix":""},{"id":369119703,"identity":"2942f423-cc07-44fa-82b0-cadc89274d5b","order_by":2,"name":"Pengpeng Zhao","email":"","orcid":"","institution":"The First Affiliated Hospital of Bengbu Medical University","correspondingAuthor":false,"prefix":"","firstName":"Pengpeng","middleName":"","lastName":"Zhao","suffix":""},{"id":369119704,"identity":"ac9d2bc2-10e4-42ba-a7d9-bd75c65a774d","order_by":3,"name":"Dongjun Yang","email":"","orcid":"","institution":"Nanjing University","correspondingAuthor":false,"prefix":"","firstName":"Dongjun","middleName":"","lastName":"Yang","suffix":""},{"id":369119705,"identity":"864f620d-7893-4c28-9799-34a957e13679","order_by":4,"name":"Yi Zou","email":"","orcid":"","institution":"China Pharmaceutical University","correspondingAuthor":false,"prefix":"","firstName":"Yi","middleName":"","lastName":"Zou","suffix":""},{"id":369119706,"identity":"9637246c-4fbb-4537-b75e-6f0fa5d5d646","order_by":5,"name":"Panhai Chen","email":"","orcid":"","institution":"China-Australia Institute of Translational Medicine Co. Ltd.","correspondingAuthor":false,"prefix":"","firstName":"Panhai","middleName":"","lastName":"Chen","suffix":""},{"id":369119707,"identity":"9ea779e6-62c8-45af-bc7c-51d7561df287","order_by":6,"name":"Dongliang Wu","email":"","orcid":"","institution":"Nanjing University","correspondingAuthor":false,"prefix":"","firstName":"Dongliang","middleName":"","lastName":"Wu","suffix":""},{"id":369119708,"identity":"0c92a58c-cdfd-42f6-91ca-3eb2091802f0","order_by":7,"name":"Wenbing Shangguan","email":"","orcid":"","institution":"Nanjing University","correspondingAuthor":false,"prefix":"","firstName":"Wenbing","middleName":"","lastName":"Shangguan","suffix":""},{"id":369119709,"identity":"6467d243-ce1b-4ff6-8025-de33763fbe46","order_by":8,"name":"Wenyang Li","email":"","orcid":"","institution":"Nanjing University","correspondingAuthor":false,"prefix":"","firstName":"Wenyang","middleName":"","lastName":"Li","suffix":""},{"id":369119710,"identity":"6b7e916f-233d-4619-bb73-992c4988c1fd","order_by":9,"name":"Xingjun Meng","email":"","orcid":"","institution":"Nanjing University","correspondingAuthor":false,"prefix":"","firstName":"Xingjun","middleName":"","lastName":"Meng","suffix":""},{"id":369119711,"identity":"4f3fc4c4-1a43-4641-9adc-e97b57189ccb","order_by":10,"name":"Mengying Xing","email":"","orcid":"","institution":"Nanjing University","correspondingAuthor":false,"prefix":"","firstName":"Mengying","middleName":"","lastName":"Xing","suffix":""},{"id":369119712,"identity":"431868b1-317d-4355-9e21-d71bec7f6f80","order_by":11,"name":"Yuzhong Chen","email":"","orcid":"","institution":"Nanjing University","correspondingAuthor":false,"prefix":"","firstName":"Yuzhong","middleName":"","lastName":"Chen","suffix":""},{"id":369119713,"identity":"6fba7084-17ba-4093-bba0-1ed28e26c7d5","order_by":12,"name":"Ming Zhang","email":"","orcid":"","institution":"China-Australia Institute of Translational Medicine Co. Ltd.","correspondingAuthor":false,"prefix":"","firstName":"Ming","middleName":"","lastName":"Zhang","suffix":""},{"id":369119714,"identity":"77b737e6-0328-46f8-b49c-879f8a76670c","order_by":13,"name":"Bing Chen","email":"","orcid":"","institution":"The Affiliated Drum Tower Hospital of Nanjing University Medical School","correspondingAuthor":false,"prefix":"","firstName":"Bing","middleName":"","lastName":"Chen","suffix":""},{"id":369119715,"identity":"a443d50c-9175-4691-8530-069b1fefff7e","order_by":14,"name":"Lingdong Kong","email":"","orcid":"","institution":"Nanjing University","correspondingAuthor":false,"prefix":"","firstName":"Lingdong","middleName":"","lastName":"Kong","suffix":""},{"id":369119716,"identity":"53e506e8-93ca-45d1-8512-fa92e3dfd428","order_by":15,"name":"Ke Zen","email":"","orcid":"","institution":"Nanjing University","correspondingAuthor":false,"prefix":"","firstName":"Ke","middleName":"","lastName":"Zen","suffix":""},{"id":369119717,"identity":"82d3118d-ba9b-460f-b7df-08cd69b42d9b","order_by":16,"name":"David C.S. Huang","email":"","orcid":"","institution":"Walter and Eliza Hall Institute of Medical Research","correspondingAuthor":false,"prefix":"","firstName":"David","middleName":"C.S.","lastName":"Huang","suffix":""},{"id":369119718,"identity":"09362956-bcb0-42cc-a714-9ae1b3fc2595","order_by":17,"name":"Zhiwei Jiang","email":"","orcid":"","institution":"The Affiliated Hospital of Nanjing University of Chinese Medicine","correspondingAuthor":false,"prefix":"","firstName":"Zhiwei","middleName":"","lastName":"Jiang","suffix":""},{"id":369119719,"identity":"6d0483c2-294e-4a54-8793-79bc9bf5d905","order_by":18,"name":"Quan Zhao","email":"data:image/png;base64,iVBORw0KGgoAAAANSUhEUgAAAZAAAAAyAQMAAABI0h/eAAAABlBMVEX///8AAABVwtN+AAAACXBIWXMAAA7EAAAOxAGVKw4bAAAAu0lEQVRIiWNgGAWjYFACHiCuYGAGMSVI0HKGZC2MbRAmcVr4zp89+OHjvDvsBgeYD97mYbDLI6hF8sC5ZMmZ254xGxxgS7bmYUguJqjF4GCPgTTvtsNALTxm0jwMBxIbCGo5zGP8m3cOSAv/NyK1HAMaztsAtoWNOC2SZ3jMLGccO8wseZjN2HKOQTJhLXznzxjf+FBzOJnvePPDG28q7AhrYTgAoZIhkWlAUD1Cix0xakfBKBgFo2CEAgDOJTlH/mbo0gAAAABJRU5ErkJggg==","orcid":"","institution":"Nanjing University","correspondingAuthor":true,"prefix":"","firstName":"Quan","middleName":"","lastName":"Zhao","suffix":""}],"badges":[],"createdAt":"2024-10-17 06:23:31","currentVersionCode":1,"declarations":"","doi":"10.21203/rs.3.rs-5280141/v1","doiUrl":"https://doi.org/10.21203/rs.3.rs-5280141/v1","draftVersion":[],"editorialEvents":[],"editorialNote":"","failedWorkflow":false,"files":[{"id":67765460,"identity":"257a6bd2-0ef3-4310-8999-36bf526496ae","added_by":"auto","created_at":"2024-10-29 13:08:00","extension":"jpg","order_by":1,"title":"Figure 1","display":"","copyAsset":false,"role":"figure","size":848641,"visible":true,"origin":"","legend":"\u003cp\u003eNONO directly interacts with nuclear PKM2. \u003cstrong\u003eA.\u003c/strong\u003eProteins biotinylated by BioID2alone or NONO-BioID2 in MDA-MB-231 cells were examined via western blotting with HRP-conjugated streptavidin following SDS‒PAGEseparation. \u003cstrong\u003eB.\u003c/strong\u003e Endogenous PKM2 was coimmunoprecipitated withanti-Flag M2 Sepharosebeads in MDA-MB-231 and BT-549 cells overexpressing Flag-tagged NONO. IgG served as the negative control. \u003cstrong\u003eC.\u003c/strong\u003e Coimmunoprecipitation of endogenous NONO with PKM2-Flag from MDA-MB-231 and BT-549 cells. \u003cstrong\u003eD.\u003c/strong\u003e The cellular localization of NONO and PKM2 in MDA-MB-231 cells was examined by immunofluorescence with anti-NONO and anti-PKM2 antibodies and by nuclear counterstaining with DAPI. \u003cstrong\u003eE.\u003c/strong\u003e A GST pull-down assay was used to detect the interaction between NONO and PKM2\u003cem\u003e in vitro\u003c/em\u003e (top). Purified GST and GST-NONO fusion proteins preabsorbed to glutathione-Sepharose beads were incubated with the prokaryotic His-PKM2 fusion protein. GST and GST-NONO fusion proteins were visualized by Coomassie blue staining (bottom). \u003cstrong\u003eF.\u003c/strong\u003e Schematic diagram of NONO truncation mutants(top). The binding of His-PKM2 fusion proteins to purified GST, GST-NONO fragments F1 (1-143 aa), F2 (1-228 aa), F3 (144-471 aa), and F4 (229-471 aa) was assessed by a GST pull-down assay (middle). GST, GST-NONO F1, F2, F3, and F4 fusion proteins were visualized by Coomassie blue staining (bottom). \u003cstrong\u003eG.\u003c/strong\u003eSchematic diagram of PKM2 in different truncated constructs (top). The binding of the His-NONO fusion protein topurified GST, GST-PKM2 fragments F1 (1-116 aa), F2 (117-218 aa), F3 (219-389 aa), and F4 (390-531 aa) was assessed by a GST pull-down assay (middle). GST, GST-PKM2 F1, F2, F3, and F4 fusion proteins were visualized by Coomassie blue staining (bottom).\u003c/p\u003e","description":"","filename":"Picture1.jpg","url":"https://assets-eu.researchsquare.com/files/rs-5280141/v1/751ffd3caa581be0862acf2a.jpg"},{"id":67764333,"identity":"485b8b8f-0fc3-4e1c-945a-863205018f3b","added_by":"auto","created_at":"2024-10-29 13:00:00","extension":"jpg","order_by":2,"title":"Figure 2","display":"","copyAsset":false,"role":"figure","size":1760568,"visible":true,"origin":"","legend":"\u003cp\u003eUpregulation of NONO is associated with poor prognosis inTNBC patients and promotes TNBC cell proliferation and metastasis \u003cem\u003ein vitro\u003c/em\u003e and \u003cem\u003ein vivo\u003c/em\u003e. \u003cstrong\u003eA. \u003c/strong\u003eRepresentative images of IHC staining of NONO in matched normal tissues (n = 60) and TNBC tissues (n = 60). Scale bar, 50 μm. \u003cstrong\u003eB.\u003c/strong\u003eQuantitative analysis of NONO expression levels in matched normal tissue (Normal) and TNBC tissue (Tumor) samples. The data are presented as the mean ± SD. ***\u003cem\u003eP\u003c/em\u003e \u0026lt; 0.001. \u003cstrong\u003eC.\u003c/strong\u003e Percentage of TNBC patients with high expression or low expression of NONO stratified according to lymph node status (N0 or N1–3) (n = 60); two-sided Fisher’s exact test, *\u003cem\u003eP\u003c/em\u003e \u0026lt; 0.05. \u003cstrong\u003eD. \u003c/strong\u003eKaplan‒Meier plot of the overall survival of TNBC patients with high expression (n = 31) or low expression (n = 29) of NONO. Long-rank test, \u003cem\u003eP\u003c/em\u003e \u0026lt; 0.05. \u003cstrong\u003eE. \u003c/strong\u003eNONO protein expression was detected by western blot in MDA-MB-231 and BT-549 cells infected with scramble control (Scr) or NONO shRNA lentivirus. GAPDH was used as a loading control. \u003cstrong\u003eF. \u003c/strong\u003eCell proliferation was examined by CCK-8 assays in MDA-MB-231 and BT-549 cells infected with Scr, NONO sh1, orNONO sh2 lentivirus. The data are presented as the mean ± SD. ****\u003cem\u003eP\u003c/em\u003e \u0026lt; 0.0001 compared to the Scr control group. \u003cstrong\u003eG. \u003c/strong\u003eColony formation assay of MDA-MB-231 and BT-549 cells with Scr control orNONO knockdown. The number of colonies isshown in the bar graph (right panels). The data are presented as the mean ± SD (n = 3). ****\u003cem\u003eP\u003c/em\u003e \u0026lt; 0.0001 compared to the Scr control group. \u003cstrong\u003eH.\u003c/strong\u003eRepresentative images of the migration (left panels) and invasion (right panels) of MDA-MB-231 and BT-549 cells in the Scr control and NONO knockdown groups. The data are presented as the mean ± SD(n = 5). ****\u003cem\u003eP\u003c/em\u003e \u0026lt; 0.0001 compared to the Scr control group. \u003cstrong\u003eI-M. \u003c/strong\u003eRepresentative images of excised tumors (\u003cstrong\u003eI\u003c/strong\u003e), tumor growth curves (\u003cstrong\u003eJ\u003c/strong\u003e), and tumor weights (\u003cstrong\u003eK\u003c/strong\u003e); representative H\u0026amp;E staining images of lungs (\u003cstrong\u003eL\u003c/strong\u003e); and images of the number of lung metastases (\u003cstrong\u003eM\u003c/strong\u003e) in MMTV-PyMT (FVB background) mice injected with Scr, NONO sh1, and NONO sh2 adeno-associated viruses (AAVs). Scale bar, 100 μm. All data are presented as the mean ± SD (n = 6). ****\u003cem\u003eP\u003c/em\u003e \u0026lt; 0.0001 compared to the Scr control group.\u003c/p\u003e","description":"","filename":"Picture2.jpg","url":"https://assets-eu.researchsquare.com/files/rs-5280141/v1/f493982781d265aa35a1c1e9.jpg"},{"id":67765461,"identity":"280991e9-f797-471b-9a45-68acb2cbf5cb","added_by":"auto","created_at":"2024-10-29 13:08:01","extension":"jpg","order_by":3,"title":"Figure 3","display":"","copyAsset":false,"role":"figure","size":1676099,"visible":true,"origin":"","legend":"\u003cp\u003ePKM2 expression is upregulated in TNBC, and knockdown of PKM2 diminishes TNBC cell proliferation and metastasis both \u003cem\u003ein vitro\u003c/em\u003e and \u003cem\u003ein vivo\u003c/em\u003e.\u003cstrong\u003e A.\u003c/strong\u003e Representative images of IHC staining of PKM2 in matched normal tissues (n = 60) and TNBC tissues (n = 60). Scale bar, 50 μm. \u003cstrong\u003eB.\u003c/strong\u003e Quantitative analysis of PKM2 expression levels in matched normal tissue (Normal) and TNBC tissue (Tumor) samples. The data are presented as the mean ± SD. **\u003cem\u003eP\u003c/em\u003e \u0026lt; 0.01.\u003cstrong\u003e C.\u003c/strong\u003e Percentage of TNBC patients with high expression or low expression of PKM2 stratified according to lymph node status (N0 or N1–3) (n = 60); two-sided Fisher’s exact test, *\u003cem\u003eP\u003c/em\u003e \u0026lt; 0.05. \u003cstrong\u003eD. \u003c/strong\u003ePKM2 protein expression was detected by western blot in MDA-MB-231 and BT-549 cells infected with the Scr, PKM2 sh1, or sh2 lentivirus. GAPDH served as a loading control. \u003cstrong\u003eE. \u003c/strong\u003eCell proliferation was examined by CCK-8 assays in MDA-MB-231 and BT-549 cells infected with the Scr, PKM2 sh1, or sh2 lentivirus. The dataare presented as the mean ± SD. ****\u003cem\u003eP\u003c/em\u003e \u0026lt; 0.0001 compared to the Scr control group. \u003cstrong\u003eF. \u003c/strong\u003eColony formation assay of MDA-MB-231 and BT-549 cells with Scr control or PKM2 knockdown. The number of colonies is shown in the bar graph (right panels). The data are presented as the mean ± SD (n = 3). ***\u003cem\u003eP\u003c/em\u003e \u0026lt; 0.001, ****\u003cem\u003eP\u003c/em\u003e \u0026lt; 0.0001 compared to the Scr control group. \u003cstrong\u003eG.\u003c/strong\u003e Representative images of the migration (top panels) and invasion (bottom panels) of MDA-MB-231 and BT-549 cells after Scr control orPKM2 knockdown. The data are presented as the mean ± SD(n = 5). ***\u003cem\u003eP\u003c/em\u003e \u0026lt; 0.001, ****\u003cem\u003eP\u003c/em\u003e \u0026lt; 0.0001 compared to the Scr control group. \u003cstrong\u003eH-L \u003c/strong\u003eRepresentative images of excised tumors (\u003cstrong\u003eH\u003c/strong\u003e), tumor growth curves (\u003cstrong\u003eI\u003c/strong\u003e), and tumor weights (\u003cstrong\u003eJ\u003c/strong\u003e); representative H\u0026amp;E staining images of lungs (\u003cstrong\u003eK\u003c/strong\u003e); and the number of lung metastases (\u003cstrong\u003eL\u003c/strong\u003e) from MMTV-PyMT (FVB background) mice injected with Scr, PKM2 sh1, or sh2 AAVs. Scale bar, 100 μm. All data are presented as the mean ± SD (n = 6). ***\u003cem\u003eP\u003c/em\u003e \u0026lt; 0.001, ****\u003cem\u003eP\u003c/em\u003e \u0026lt; 0.0001 compared to the Scr control group.\u003c/p\u003e","description":"","filename":"Picture3.jpg","url":"https://assets-eu.researchsquare.com/files/rs-5280141/v1/88845694e8af79b342c1d74d.jpg"},{"id":67764335,"identity":"b88a98e4-b718-41d8-87d2-a291c5feb782","added_by":"auto","created_at":"2024-10-29 13:00:00","extension":"jpg","order_by":4,"title":"Figure 4","display":"","copyAsset":false,"role":"figure","size":1757551,"visible":true,"origin":"","legend":"\u003cp\u003e\u003cem\u003eSERPINE1\u003c/em\u003e is a key transcriptional target of NONO and PKM2 in TNBC.\u003cstrong\u003e A.\u003c/strong\u003e Venn diagram depicting the overlap of NONO- and PKM2-regulated differentially expressedgenes (DEGs) in MDA-MB-231 cells obtained from RNA-seq analysis. \u003cstrong\u003eB.\u003c/strong\u003e Heatmap showing the top 20 most differentially expressed genes whose expression was coupregulated orcodownregulated by NONO or PKM2. NC: negative control; KD: knockdown. \u003cstrong\u003eC. \u003c/strong\u003eRelative mRNA levels of \u003cem\u003eSERPINE1\u003c/em\u003e, \u003cem\u003eIL11\u003c/em\u003e, \u003cem\u003eCCN2\u003c/em\u003e, \u003cem\u003eRCN1\u003c/em\u003e, \u003cem\u003eVDAC1\u003c/em\u003e, \u003cem\u003eCDKN1A\u003c/em\u003e, \u003cem\u003eADAMTSL4\u003c/em\u003e, \u003cem\u003eMATN2\u003c/em\u003e, \u003cem\u003eFERMT2\u003c/em\u003e and \u003cem\u003eMCAM\u003c/em\u003enormalized to those of \u003cem\u003eGAPDH\u003c/em\u003ewere examined by RT‒qPCR in negative control (NC) or NONO-silenced MDA-MB-231 cells. The data are presented as the mean ± SD (n = 3). *\u003cem\u003eP\u003c/em\u003e \u0026lt; 0.05, **\u003cem\u003eP\u003c/em\u003e \u0026lt; 0.01, ***\u003cem\u003eP\u003c/em\u003e \u0026lt; 0.001, ****\u003cem\u003eP\u003c/em\u003e \u0026lt; 0.0001 compared to NC. \u003cstrong\u003eD.\u003c/strong\u003eThe protein expression of PAI-1 in NC and NONO-KD MDA-MB-231 cells was assessed by western blot analyses with the indicated antibodies. \u003cstrong\u003eE. \u003c/strong\u003eWestern blot analysis of the indicated proteins in MDA-MB-231 cells treated with NC, NONO-KD, orNONO-KD + PAI-1. GAPDH served as a loading control.\u003cstrong\u003e F.\u003c/strong\u003e Cell proliferation was examined by a CCK-8 assay in MDA-MB-231 cells treated with NC, NONO-KD, or NONO-KD + PAI-1. The data are presented as the mean ± SD (n = 5). ****\u003cem\u003eP\u003c/em\u003e \u0026lt; 0.0001 compared to the NONO-KD group. \u003cstrong\u003eG.\u003c/strong\u003eColony formation was determined in MDA-MB-231 cells treated with NC, NONO-KD, or NONO-KD + PAI-1. The data are presented as the mean ± SD (n = 3). **\u003cem\u003eP\u003c/em\u003e \u0026lt; 0.01, ***\u003cem\u003eP\u003c/em\u003e \u0026lt; 0.001 compared to the corresponding control. \u003cstrong\u003eH.\u003c/strong\u003e Representative images of the migration (top panels) and invasion (bottom panels) of MDA-MB-231 cells treated with NC, NONO-KD, or NONO-KD + PAI-1. The data are presented as the mean ± SD (n = 5). ***\u003cem\u003eP\u003c/em\u003e \u0026lt; 0.001, ****\u003cem\u003eP\u003c/em\u003e \u0026lt; 0.0001 compared to the corresponding control. \u003cstrong\u003eI-K.\u003c/strong\u003e Photographs (\u003cstrong\u003eI\u003c/strong\u003e), tumor growth curves (\u003cstrong\u003eJ\u003c/strong\u003e), and tumor weights (\u003cstrong\u003eK\u003c/strong\u003e) of MDA-MB-231 xenograft tumors from the scrambled (Scr), NONO-KD, and NONO-KD + PAI-1 groups. The data are presented as the mean ± SD (n = 6). ***\u003cem\u003eP\u003c/em\u003e \u0026lt; 0.001, ****\u003cem\u003eP\u003c/em\u003e \u0026lt; 0.0001 compared to the corresponding control. \u003cstrong\u003eL. \u003c/strong\u003eRelative mRNA levels of \u003cem\u003eSERPINE1\u003c/em\u003e, \u003cem\u003eIL11\u003c/em\u003e, \u003cem\u003eCCN2\u003c/em\u003e, \u003cem\u003eRCN1\u003c/em\u003e, \u003cem\u003eVDAC1\u003c/em\u003e, \u003cem\u003eCDKN1A\u003c/em\u003e, \u003cem\u003eADAMTSL4\u003c/em\u003e, \u003cem\u003eMATN2\u003c/em\u003e, \u003cem\u003eFERMT2\u003c/em\u003e and \u003cem\u003eMCAM\u003c/em\u003e (normalized to \u003cem\u003eGAPDH\u003c/em\u003e) were examined by RT‒qPCR in NC and PKM2-KD MDA-MB-231 cells. The data are presented as the mean ± SD(n = 3). **\u003cem\u003eP\u003c/em\u003e \u0026lt; 0.01, ***\u003cem\u003eP\u003c/em\u003e \u0026lt; 0.001, ****\u003cem\u003eP\u003c/em\u003e \u0026lt; 0.0001 compared to NC. \u003cstrong\u003eM. \u003c/strong\u003eThe protein expression of PAI-1 in NC and PKM2-KD MDA-MB-231 cells was assessed by western blot analyses with the indicated antibodies. \u003cstrong\u003eN. \u003c/strong\u003eWestern blot analysis of the indicated proteins in MDA-MB-231 cells treated with NC, PKM2-KD, orPKM2-KD + PAI-1. GAPDH served as a loading control. \u003cstrong\u003eO.\u003c/strong\u003e Cell proliferation was examined by a CCK-8 assay in MDA-MB-231 cells treated with NC, PKM2-KD, or PKM2-KD + PAI-1. The data are presented as the mean ± SD (n = 5). ***\u003cem\u003eP\u003c/em\u003e \u0026lt; 0.001 compared to the PKM2-KD group. \u003cstrong\u003eP. \u003c/strong\u003eColony formation was determined in MDA-MB-231 cells treated with NC, PKM2-KD, or PKM2-KD + PAI-1. The data are presented as the mean ± SD (n = 3). **\u003cem\u003eP\u003c/em\u003e \u0026lt; 0.01, ***\u003cem\u003eP\u003c/em\u003e \u0026lt; 0.001 compared with the PKM2-KD group. \u003cstrong\u003eQ.\u003c/strong\u003e Representative images of the migration (top panels) and invasion (bottom panels) of MDA-MB-231 cells treated with NC, PKM2-KD, orPKM2-KD + PAI-1. The data are presented as the mean ± SD(n = 5). **\u003cem\u003eP\u003c/em\u003e \u0026lt; 0.01, ****\u003cem\u003eP\u003c/em\u003e \u0026lt; 0.0001 compared to the corresponding control. \u003cstrong\u003eR.\u003c/strong\u003e Pearson correlation scatter plot of H scores forNONO, PKM2, and PAI-1 in human TNBC tissues (n = 60).\u003c/p\u003e","description":"","filename":"Picture4.jpg","url":"https://assets-eu.researchsquare.com/files/rs-5280141/v1/2c08585040a10ba864027e26.jpg"},{"id":67765462,"identity":"a47f5890-35bd-427c-8662-42f4314cc2a8","added_by":"auto","created_at":"2024-10-29 13:08:01","extension":"jpg","order_by":5,"title":"Figure 5","display":"","copyAsset":false,"role":"figure","size":1251950,"visible":true,"origin":"","legend":"\u003cp\u003eNONO-dependent PKM2 and its nuclear protein kinase activity are critical for \u003cem\u003eSERPINE1\u003c/em\u003etranscription and TNBC progression.\u003cstrong\u003e A \u003c/strong\u003eand \u003cstrong\u003eB.\u003c/strong\u003e The protein and mRNA expression of PAI-1 wasassessed by western blot (\u003cstrong\u003eA\u003c/strong\u003e) and RT‒qPCR(\u003cstrong\u003eB\u003c/strong\u003e) analyses in NC and NONO-KD MDA-MB-231 cells with or without PKM2 overexpression. GAPDH served as a loading control. The data are presented as the mean ± SD(n = 3). **\u003cem\u003eP\u003c/em\u003e \u0026lt; 0.01, N.S. (not significant) compared to the corresponding control. \u003cstrong\u003eC. \u003c/strong\u003eChIP‒qPCR was used to assess the enrichment of H3T11ph on \u003cem\u003eSERPINE1 \u003c/em\u003eat the TSS in NC and NONO-KD MDA-MB-231 cells. IgG served as a negative control. The data are presented as the mean ± SD(n = 3). ***\u003cem\u003eP\u003c/em\u003e \u0026lt; 0.001 compared to the NC group. \u003cstrong\u003eD.\u003c/strong\u003eWestern blot analysis of the indicated protein levels in NC cells, PKM2-KD cells, PKM2-KD + PKM2-WT cells, PKM2-KD + PKM2-Y105F cells and PKM2-KD + PKM2-R399E cells. GAPDH served as a loading control. \u003cstrong\u003eE.\u003c/strong\u003e RT‒qPCRanalysis of the mRNA levels of \u003cem\u003eSERPINE1\u003c/em\u003e (normalized to the level of \u003cem\u003eGAPDH\u003c/em\u003e) in NC cells, PKM2-KD cells, PKM2-KD + PKM2-WT cells, PKM2-KD + PKM2-Y105F cells and PKM2-KD + PKM2-R399E cells. The data are presented as the mean ± SD (n = 3). **\u003cem\u003eP\u003c/em\u003e \u0026lt; 0.01, ***\u003cem\u003eP\u003c/em\u003e \u0026lt; 0.001, N.S. (notsignificant) compared to the corresponding control. \u003cstrong\u003eF. \u003c/strong\u003eA\u003cstrong\u003e \u003c/strong\u003eGST pull-down assay was utilized to examine the binding of prokaryotic GST, wild-type (WT) GST-PKM2 and GST-PKM2 point mutants with purified His-NONO fusion proteins (top). GST, GST-PKM2 WT, and diverse GST-PKM2 point mutants were visualized by Commassie staining (bottom). \u003cstrong\u003eG.\u003c/strong\u003eEndogenous NONO was coimmunoprecipitated in MDA-MB-231 cells overexpressing Flag-tagged PKM2-WT and PKM2-S406A. IgG served as the negative control. \u003cstrong\u003eH.\u003c/strong\u003e The distribution of endogenous PKM2 and exogenous PKM2-Flag proteins in the nucleus and cytoplasm in MDA-MB-231 cells overexpressing Flag-tagged PKM2-WT and PKM2-S406A was examined by western blot. GAPDH and Lamin B1 served as loading controls. \u003cstrong\u003eI.\u003c/strong\u003eWestern blot analysis of the indicated proteins in PKM2-WT- and PKM2-S406A-overexpressing MDA-MB-231 cells. GAPDH and histone H3 served as loading controls. \u003cstrong\u003eJ.\u003c/strong\u003e RT‒qPCR analysis of the mRNA levels of \u003cem\u003eSERPINE1\u003c/em\u003e(normalized to the level of \u003cem\u003eGAPDH\u003c/em\u003e) in MDA-MB-231 cells overexpressing PKM2-WT or thePKM2-S406A mutant. The data are presented as the mean ± SD(n = 3). ***\u003cem\u003eP\u003c/em\u003e \u0026lt; 0.001.\u003cstrong\u003e K. \u003c/strong\u003eCell proliferation was examined by CCK-8 assays in MDA-MB-231 cells overexpressing PKM2-WT or thePKM2-S406A mutant. \u003cstrong\u003eL.\u003c/strong\u003e Colony formation assay of MDA-MB-231 cells overexpressing PKM2-WT and the PKM2-S406A mutant. The number of colonies is shown in the bar graph (right panels). The data are presented as the mean ± SD (n = 3). **\u003cem\u003eP\u003c/em\u003e \u0026lt; 0.01 compared to the PKM2-WT group. \u003cstrong\u003eM.\u003c/strong\u003eRepresentative images of the migration (top panels) and invasion (bottom panels) of MDA-MB-231 cells overexpressing PKM2-WT or the PKM2-S406A mutant. The data are presented as the mean ± SD (n = 5). ***\u003cem\u003eP\u003c/em\u003e \u0026lt; 0.001 compared to the corresponding control.\u003c/p\u003e","description":"","filename":"Picture5.jpg","url":"https://assets-eu.researchsquare.com/files/rs-5280141/v1/bcd1a9cc24d929b971d8ecf6.jpg"},{"id":67764338,"identity":"78a960e6-6e3b-4f25-9bf3-9fb4aa8ab4af","added_by":"auto","created_at":"2024-10-29 13:00:01","extension":"jpg","order_by":6,"title":"Figure 6","display":"","copyAsset":false,"role":"figure","size":1561525,"visible":true,"origin":"","legend":"\u003cp\u003eNONO and PKM2-mediated H3T11ph coordinate with H3K27ac on \u003cem\u003eSERPINE1\u003c/em\u003e gene loci.\u003cstrong\u003e A.\u003c/strong\u003eWestern blot analysis of the indicated histone H3 modifications in NC and PKM2-silenced MDA-MB-231 cells. Histone H3 served as a loading control. \u003cstrong\u003eB.\u003c/strong\u003e Heatmaps of CUT\u0026amp;Tag data showing that NONO, H3T11ph, and H3K27ac levels at the transcription start site (TSS) significantly decreased (Decreased) or unchanged (Others) in the NC, NONO-KD, or PKM2-KD MDA-MB-231 cells, respectively. \u003cstrong\u003eC.\u003c/strong\u003e Integrative Genomics Viewer (IGV) tracks representing the signals of NONO, H3T11ph, and H3K27ac at \u003cem\u003eSERPINE1\u003c/em\u003e gene loci from CUT\u0026amp;Tag data in MDA-MB-231 cells. \u003cstrong\u003eD. \u003c/strong\u003eChIP‒qPCR analysis of the enrichment of NONO, H3T11ph, and H3K27ac at \u003cem\u003eSERPINE1\u003c/em\u003e gene loci at the indicated positions as in (\u003cstrong\u003eC)\u003c/strong\u003e in MDA-MB-231 cells. IgG served as a negative control. The data are presented as the mean ± SD(n = 3). *\u003cem\u003eP\u003c/em\u003e \u0026lt; 0.05, **\u003cem\u003eP \u003c/em\u003e\u0026lt; 0.01, ***\u003cem\u003eP\u003c/em\u003e \u0026lt; 0.001, and\u003cem\u003e \u003c/em\u003e****\u003cem\u003eP\u003c/em\u003e \u0026lt; 0.0001 compared to the corresponding control.\u003c/p\u003e","description":"","filename":"Picture6.jpg","url":"https://assets-eu.researchsquare.com/files/rs-5280141/v1/d50c1f325821377d4dd93f82.jpg"},{"id":67764336,"identity":"112980e0-19bd-4965-bcfa-ab274e8311f2","added_by":"auto","created_at":"2024-10-29 13:00:00","extension":"jpg","order_by":7,"title":"Figure 7","display":"","copyAsset":false,"role":"figure","size":1540367,"visible":true,"origin":"","legend":"\u003cp\u003eNONO or PKM2 deficiency reduces PAI-1 expression and inhibits the malignant progression of spontaneous mammary tumors in mice.\u003cstrong\u003e A.\u003c/strong\u003e Breeding strategy for mammary-specific NONO-knockout (KO) transgenic mice. The genotype of the NONO-KO female mice was Cre\u003csup\u003e+/-\u003c/sup\u003e::PyMT\u003csup\u003e+\u003c/sup\u003e::NONO\u003csup\u003efl/fl\u003c/sup\u003e, and Cre\u003csup\u003e-/-\u003c/sup\u003e::PyMT\u003csup\u003e+\u003c/sup\u003e::NONO\u003csup\u003efl/fl\u003c/sup\u003e female mice were used as control mice. \u003cstrong\u003eB-D. \u003c/strong\u003eRepresentative images of excised tumors (\u003cstrong\u003eB\u003c/strong\u003e), tumor growth curves (\u003cstrong\u003eC\u003c/strong\u003e), representative H\u0026amp;E staining images of lungs (left panels) and the number of lung metastases (right panels) (\u003cstrong\u003eD\u003c/strong\u003e) from control (n = 6) and NONO-KO (n = 8) mice. Scale bar, 100 μm. All data are presented as the mean ± SD. **\u003cem\u003eP \u003c/em\u003e\u0026lt; 0.01 compared to the control group. \u003cstrong\u003eE.\u003c/strong\u003e Western blot analysis of the indicated proteins in tumors extracted from control and NONO-KO mice. GAPDH served as a loading control. \u003cstrong\u003eF.\u003c/strong\u003e Representative H\u0026amp;E staining and IHC staining of NONO, PAI-1, and Ki-67 in mammary tumor tissues from MMTV-PyMT mice (C57BL/6 background) in the control and NONO-KO groups. Scale bar, 25 μm. \u003cstrong\u003eG.\u003c/strong\u003e Breeding strategy for mammary-specific PKM2-knockout (KO) transgenic mice. The genotype of the PKM2-KO female mice was Cre\u003csup\u003e+/-\u003c/sup\u003e::PyMT\u003csup\u003e+\u003c/sup\u003e::PKM2\u003csup\u003efl/fl\u003c/sup\u003e, and Cre\u003csup\u003e-/-\u003c/sup\u003e::PyMT\u003csup\u003e+\u003c/sup\u003e::PKM2\u003csup\u003efl/fl\u003c/sup\u003e female mice were used as control mice.\u003cstrong\u003e H-I. \u003c/strong\u003eRepresentative images of excised tumors (\u003cstrong\u003eH\u003c/strong\u003e), tumor growth curves (\u003cstrong\u003eI\u003c/strong\u003e), representative H\u0026amp;E staining images of lungs (left panels) and the number of lung metastases (right panels) (\u003cstrong\u003eJ\u003c/strong\u003e) from control (n = 5) and PKM2-KO (n = 5) mice. Scale bar, 100 μm. All data are presented as the mean ± SD. **\u003cem\u003eP \u003c/em\u003e\u0026lt; 0.01 compared to the control group. \u003cstrong\u003eK.\u003c/strong\u003e Western blot analysis of the indicated proteins in tumors extracted from control and PKM2-KO mice. GAPDH and histone H3 served as loading controls. \u003cstrong\u003eL.\u003c/strong\u003e Representative H\u0026amp;E staining and IHC staining of PKM2, PAI-1, H3T11ph and Ki-67 in mammary tumor tissues from MMTV-PyMT mice in the control and PKM2-KO groups. Scale bar, 25 μm.\u003c/p\u003e","description":"","filename":"Picture7.jpg","url":"https://assets-eu.researchsquare.com/files/rs-5280141/v1/e0df83fd0321cdeadbb21ae3.jpg"},{"id":68869649,"identity":"3cd230af-e497-4981-89b0-b35bf337bf36","added_by":"auto","created_at":"2024-11-13 02:47:11","extension":"pdf","order_by":0,"title":"","display":"","copyAsset":false,"role":"manuscript-pdf","size":11451985,"visible":true,"origin":"","legend":"","description":"","filename":"manuscript.pdf","url":"https://assets-eu.researchsquare.com/files/rs-5280141/v1/949e76a8-fc5a-420d-a466-cb056529f9fa.pdf"},{"id":67764341,"identity":"05d1c901-cd1f-4bf7-9481-c34d4871f512","added_by":"auto","created_at":"2024-10-29 13:00:01","extension":"docx","order_by":1,"title":"","display":"","copyAsset":false,"role":"supplement","size":37988064,"visible":true,"origin":"","legend":"","description":"","filename":"LiAddfiles.docx","url":"https://assets-eu.researchsquare.com/files/rs-5280141/v1/694d0a313197d66c748b335d.docx"}],"financialInterests":"No competing interests reported.","formattedTitle":"NONO directs PKM2-mediated H3T11ph to promote triple-negative breast cancer metastasis by activating SERPINE1 expression","fulltext":[{"header":"Background","content":"\u003cp\u003eThe latest international cancer survey report shows that there are approximately 20\u0026nbsp;million new cancer cases and 9.7\u0026nbsp;million cancer deaths worldwide in the year 2022, among which breast cancer ranks second for approximately 2.3\u0026nbsp;million new cases and fourth for approximately 0.67\u0026nbsp;million deaths [\u003cspan citationid=\"CR1\" class=\"CitationRef\"\u003e1\u003c/span\u003e]. Triple-negative breast cancer (TNBC) is a type of breast cancer that lacks the expression of estrogen receptor (ER), progesterone receptor (PR), and human epidermal growth factor receptor 2 (HER2) and has high malignancy, easy metastasis, and poor prognosis [\u003cspan citationid=\"CR2\" class=\"CitationRef\"\u003e2\u003c/span\u003e]. Currently, owing to the lack of specific and effective therapeutic targets, treatments for TNBC are limited, resulting in a shorter survival time for patients with TNBC. The mortality rate within five years of diagnosis for TNBC is as high as 40%, seriously threatening the physical and mental health of women [\u003cspan citationid=\"CR3\" class=\"CitationRef\"\u003e3\u003c/span\u003e]. Therefore, there is an urgent need to explore the pathogenesis and therapeutic strategies of TNBC.\u003c/p\u003e \u003cp\u003eTranscriptional dysregulation has been recognized as a hallmark of cancer, where abnormal gene expression leads to tumor initiation and malignant progression [\u003cspan citationid=\"CR4\" class=\"CitationRef\"\u003e4\u003c/span\u003e, \u003cspan citationid=\"CR5\" class=\"CitationRef\"\u003e5\u003c/span\u003e]. The aberrant interplay between transcription factors and epigenetic regulators is key to cancer pathogenesis [\u003cspan citationid=\"CR6\" class=\"CitationRef\"\u003e6\u003c/span\u003e]. The multifunctional nuclear protein NONO (also known as P54nrb) was initially defined as a non-POU domain-containing octamer-binding protein belonging to the Drosophila behavior/human splicing (DBHS) family [\u003cspan citationid=\"CR7\" class=\"CitationRef\"\u003e7\u003c/span\u003e, \u003cspan citationid=\"CR8\" class=\"CitationRef\"\u003e8\u003c/span\u003e]. The protein structure of NONO contains RNA and DNA-binding domains, allowing it to participate in important biological processes such as precursor mRNA splicing, transcriptional regulation, nuclear retention of defective RNA, and DNA damage repair [\u003cspan citationid=\"CR9\" class=\"CitationRef\"\u003e9\u003c/span\u003e]. Our recent study revealed that the interaction between the transcription factors NONO and SOX6 synergistically silences γ-globin gene transcription in human erythroid cells [\u003cspan citationid=\"CR10\" class=\"CitationRef\"\u003e10\u003c/span\u003e]. The C-terminus of NONO has a nuclear localization sequence that assists in its distribution mainly in the nucleus and serves as an important component of paraspeckles [\u003cspan citationid=\"CR11\" class=\"CitationRef\"\u003e11\u003c/span\u003e]. However, NONO rarely functions alone and often interacts with other effector proteins to exert its biological effects [\u003cspan citationid=\"CR12\" class=\"CitationRef\"\u003e12\u003c/span\u003e].\u003c/p\u003e \u003cp\u003eIn fact, as a binding protein of the TNBC subtype-specific and highly expressed membrane spike protein Moesin (MSN), NONO plays an important role in guiding the localization of MSN to nuclei and subsequent CREB phosphorylation activation to regulate TNBC progression [\u003cspan citationid=\"CR13\" class=\"CitationRef\"\u003e13\u003c/span\u003e]. Additionally, NONO can bind to EGFR in the nucleus to increase its stability and recruit CBP/P300 to enhance the transcriptional activity of EGFR, thereby enhancing nuclear EGFR-mediated tumorigenesis of TNBC [\u003cspan citationid=\"CR14\" class=\"CitationRef\"\u003e14\u003c/span\u003e]. NONO can also bind to IGFBP3 to activate PARP-dependent DNA damage repair, thereby increasing TNBC chemotherapy tolerance [\u003cspan citationid=\"CR15\" class=\"CitationRef\"\u003e15\u003c/span\u003e]. These studies clearly indicate that NONO is crucial for the development of TNBC. However, little is known about whether and how NONO, as a transcription factor, promotes malignant progression or metastasis of TNBC.\u003c/p\u003e \u003cp\u003ePyruvate kinase (PK), a rate-limiting enzyme in glycolysis, catalyzes the transfer of a phosphate group from phosphoenolpyruvate (PEP) to adenosine diphosphate (ADP) to yield pyruvate and ATP [\u003cspan citationid=\"CR16\" class=\"CitationRef\"\u003e16\u003c/span\u003e]. In the mammalian genome, the PKM1 and PKM2 isoforms are alternatively spliced products of the \u003cem\u003ePKM\u003c/em\u003e gene by mutually exclusive use of exon 9 or exon 10, respectively. PKM1 is distributed in many normal differentiated tissues, whereas PKM2 is mainly expressed in most proliferating cells, including fetal and cancerous cells [\u003cspan citationid=\"CR17\" class=\"CitationRef\"\u003e17\u003c/span\u003e, \u003cspan citationid=\"CR18\" class=\"CitationRef\"\u003e18\u003c/span\u003e]. PKM2 has been characterized as a unique biomarker in cancer and has been shown to promote cancer cell proliferation and metastasis by driving the Warburg effect. However, its role in tumorigenesis in different cancers is controversial [\u003cspan citationid=\"CR17\" class=\"CitationRef\"\u003e17\u003c/span\u003e, \u003cspan citationid=\"CR18\" class=\"CitationRef\"\u003e18\u003c/span\u003e]. Importantly, in addition to its canonical metabolic enzyme function, PKM2 can translocate into the nucleus and function as a protein kinase and transcriptional co-activator [\u003cspan citationid=\"CR19\" class=\"CitationRef\"\u003e19\u003c/span\u003e, \u003cspan citationid=\"CR20\" class=\"CitationRef\"\u003e20\u003c/span\u003e]. PKM2 phosphorylates histone H3 at threonine 11 (H3T11ph), which is implicated in transcriptional activation [\u003cspan citationid=\"CR21\" class=\"CitationRef\"\u003e21\u003c/span\u003e]. However, the molecular mechanisms by which PKM2 is recruited to participate in gene transcriptional regulation and is precisely enriched across the genome within the nucleus are poorly understood.\u003c/p\u003e \u003cp\u003eIn this study, we found that NONO and PKM2 are important regulatory molecules involved in TNBC metastasis. We showed that NONO can specifically recruit PKM2 to coordinate the phosphorylation of threonine 11 of histone H3 (H3T11ph) and the acetylation of lysine 27 of histone H3 (H3K27ac), activating the transcription of multiple key genes, such as \u003cem\u003eSERPINE1\u003c/em\u003e (serine protease inhibitor family E member 1, encoding the PAI-1 protein) [\u003cspan citationid=\"CR22\" class=\"CitationRef\"\u003e22\u003c/span\u003e, \u003cspan citationid=\"CR23\" class=\"CitationRef\"\u003e23\u003c/span\u003e], thus promoting the migration and metastasis of TNBC cells. PAI-1 facilitates tumor cell detachment from the matrix and promotes tumor dissemination and metastasis and has been recommended as a promising biomarker for poor prognosis in primary breast cancer patients by the American Society of Clinical Oncology (ASCO) and the European Organization for Research and Treatment of Cancer (EORTC) clinical operation guidelines [\u003cspan citationid=\"CR22\" class=\"CitationRef\"\u003e22\u003c/span\u003e, \u003cspan citationid=\"CR23\" class=\"CitationRef\"\u003e23\u003c/span\u003e]. Our study revealed that NONO-dependent PKM2 coordinates histone H3 phosphorylation and acetylation to promote gene transcription and metastasis in TNBC cells.\u003c/p\u003e"},{"header":"Methods","content":"\u003cdiv id=\"Sec3\" class=\"Section2\"\u003e \u003ch2\u003eCell culture\u003c/h2\u003e \u003cp\u003eHuman embryonic kidney (HEK293T) cells and two human TNBC cell lines (MDA-MB-231 and BT-549) were obtained from Shanghai Institute of Cell Biology, Chinese Academy of Sciences (Shanghai, China). MDA-MB-231 and HEK293T cells were cultured in Dulbecco\u0026rsquo;s modified Eagle\u0026rsquo;s medium (DMEM) (Gibco), and BT-549 cells were cultured in RPMI-1640 medium (Gibco) supplemented with 10% FBS (ExCell Bio) and 1% penicillin-streptomycin (100 U/ml, 100 \u0026micro;g/ml; Gibco). Cells were maintained at 37\u0026deg;C in a humidified incubator with 5% carbon dioxide. Cells were authenticated by short tandem repeat (STR) profiling and were negative for mycoplasma contamination.\u003c/p\u003e \u003c/div\u003e\n\u003ch3\u003esiRNA infection and shRNA lentiviral transduction\u003c/h3\u003e\n\u003cp\u003eThe shRNA lentivirus was produced in HEK293T cells by co-transfection with PLKO.1-shRNA, the viral envelope plasmid pMD2. G, and the viral packaging plasmid psPAX2 using Lipofectamine 3000 (Invitrogen) following the manufacturer\u0026rsquo;s instructions. The scrambled (Scr) sequence was used as the negative control. At 48 h after infection, the viral supernatants were harvested and used to infect cells or stored at -80\u0026deg;C. To obtain stable cell lines, the cells were selected using 1 \u0026micro;g/mL puromycin (Yeasen, 60209ES100). The Scr and shRNA sequences used were as follows.\u003c/p\u003e \u003cp\u003eScr: 5\u0026rsquo;-CCTAAGGTTAAGTCGCCCTCG-3\u0026rsquo;\u003c/p\u003e \u003cp\u003ehuman NONO shRNA-1: 5\u0026rsquo;-CAGGCGAAGTCTTCATTCATA-3\u0026rsquo;\u003c/p\u003e \u003cp\u003ehuman NONO shRNA-2: 5\u0026rsquo;-TCCAGAGAAGCTGGTTATAAA-3\u0026rsquo;;\u003c/p\u003e \u003cp\u003ehuman PKM2 shRNA-1: 5\u0026rsquo;-CTACCACTTGCAATTATTTGA-3\u0026rsquo;\u003c/p\u003e \u003cp\u003ehuman PKM2 shRNA-2: 5\u0026rsquo;-CCACTTGCAATTATTTGAGGA-3\u0026rsquo;\u003c/p\u003e \u003cp\u003eNegative control (NC) and specific siRNAs against NONO, PKM2, and TIP60 were synthesized by GenePharma (Suzhou, China). Cells were transiently transfected with 25 nM siRNA using the Lipofectamine 3000 transfection reagent. The siRNA sequences used were as follows:\u003c/p\u003e\n\u003ch3\u003eNC: 5’-UUCUCCGAACGUGUCACGU-3’\u003c/h3\u003e\n\u003cp\u003ehuman NONO siRNA-1: 5\u0026rsquo;-CCUUACAGUUCGAAACCUU-3\u0026rsquo;;\u003c/p\u003e \u003cp\u003ehuman NONO siRNA-2: 5\u0026rsquo;-GGAAGGCACUCAUUGAGAU-3\u0026rsquo;;\u003c/p\u003e \u003cp\u003ehuman PKM2 siRNA-1: 5\u0026rsquo;-CCAUAAUCGUCCUCACCAA-3\u0026rsquo;\u003c/p\u003e \u003cp\u003ehuman PKM2 siRNA-2: 5\u0026rsquo;-GCCAUAAUCGUCCUCACCA-3\u0026rsquo;;\u003c/p\u003e \u003cp\u003ehuman TIP60 siRNA-1: 5\u0026rsquo;-GGACAGCUCUGAUGGAAUA-3\u0026rsquo;;\u003c/p\u003e \u003cp\u003ehuman TIP60 siRNA-2: 5\u0026rsquo;-GAUCGAGUUCAGCUAUGAA-3\u0026rsquo;;\u003c/p\u003e \u003cp\u003eTo overexpress PAI-1, human \u003cem\u003eSERPINE1\u003c/em\u003e cDNA was cloned and inserted into the lentiviral vector pLVX-IRES-mCherry at EcoRI and XbaI sites. Human \u003cem\u003eKAT5\u003c/em\u003e cDNA was cloned and inserted into the pcDNA3.1(+) vector at BamHI and XhoI sites for TIP60 overexpression.\u003c/p\u003e\n\u003ch3\u003eCell proliferation, migration and invasion assays\u003c/h3\u003e\n\u003cp\u003eFor the CCK-8 assay, cells were plated in 96-well plates at a concentration of 1.5 \u0026times; 10\u003csup\u003e3\u003c/sup\u003e cells per well. After the addition of CCK-8 reagent (Vazyme Biotech, A311-01), the cells were incubated for 1.5 h at 37\u0026deg;C, after which absorbance at a wavelength of 450 nm was detected to construct a growth curve.\u003c/p\u003e \u003cp\u003eFor the colony formation assay, cells were seeded in 6-well plates at a density of 1 \u0026times; 10\u003csup\u003e3\u003c/sup\u003e cells/well and cultured for 10 days. The cloned cells were fixed with 4% paraformaldehyde (PFA) for 30 min and stained with 0.1% crystal violet solution for 30 min. Finally, colonies were washed with distilled water, dried, and photographed.\u003c/p\u003e \u003cp\u003eFor cell migration assays, 3.5 \u0026times; 10\u003csup\u003e4\u003c/sup\u003e cells were seeded on the chamber inserts of the Transwell apparatus (Corning, 3422) in serum-free medium, and medium supplemented with 10% FBS was added to the bottom chamber. After 12 h, the uninvaded cells on the upper surface of the Transwell chamber were removed using a moistened cotton swab. The migrated cells on the lower membrane surface were fixed with 4% PFA for 30 min and stained with a 0.1% crystal violet solution for 30 min. Imaging was performed using a fluorescence microscope at \u0026times;100 magnification, and images (six fields per membrane) were acquired using ImageJ software. The invasion assay was performed as described for the migration assay, except that the upper chamber was precoated with 50 \u0026micro;l of Matrigel solution.\u003c/p\u003e\n\u003ch3\u003eWestern blot analysis\u003c/h3\u003e\n\u003cdiv class=\"Heading\"\u003eWestern blot analysis\u003c/div\u003e \u003cp\u003eTotal cell proteins were extracted using a cell lysis buffer (Beyotime, P0013) for western blotting and immunoprecipitation. Histone proteins were extracted using a standard protocol for acid extraction of histones from chromatin as previously reported [\u003cspan citationid=\"CR24\" class=\"CitationRef\"\u003e24\u003c/span\u003e]. Proteins were separated using 10% or 15% SDS-PAGE and transferred onto polyvinylidene difluoride (PVDF) membranes (Roche, Basel, Switzerland). The membranes were blocked for 1 h at room temperature in either 5% nonfat milk or BSA (Sigma) and then incubated with primary antibodies overnight at 4\u0026deg;C. After incubation with secondary antibodies, the protein bands were visualized using enhanced chemiluminescence (Tanon). All the primary antibodies used in this study are listed in Additional file 2: Table S4.\u003c/p\u003e \u003cdiv id=\"Sec8\" class=\"Section2\"\u003e \u003ch2\u003eQuantitative real-time PCR analysis (RT‒qPCR)\u003c/h2\u003e \u003cp\u003eTotal RNA was prepared using TRIzol reagent (Invitrogen) according to the manufacturer\u0026rsquo;s instructions and assessed using a Nanodrop 2000 spectrophotometer (Thermo Fisher Scientific). Complementary DNAs (cDNAs) was produced using a HiScript II 1st Strand cDNA Synthesis Kit (Vazyme Biotech, R212-01). Quantitative real-time PCR analysis was performed using the AceQ qPCR SYBR Green Master Mix (Vazyme Biotech, R121-02) in a StepOnePlus RT‒PCR system (Thermo Fisher Scientific). GAPDH was used as a loading control. The primers used for qRT-PCR are listed in Additional file 2: Table S5.\u003c/p\u003e \u003c/div\u003e\n\u003ch3\u003eBioID2 pull-down and mass spectrometry analysis\u003c/h3\u003e\n\u003cp\u003eBioID2 pull-down experiments were performed as previously described with minor modifications [\u003cspan citationid=\"CR25\" class=\"CitationRef\"\u003e25\u003c/span\u003e]. Briefly, MDA-MB-231 cells transduced with the NONO-BioID2 fusion protein or BioID2-only control were seeded in 10-cm dishes. When the cells reached 80% confluence, the medium was replaced with complete medium containing 50 \u0026micro;M biotin (Sigma, B4501) and the cells were cultured for 16\u0026ndash;18 h. The cells were subsequently lysed in lysis buffer (50 mM Tris HCl (pH 7.4), 500 mM NaCl, 0.2% SDS, 1 mM DTT, and 1\u0026times; protease inhibitors), 0.1 \u0026micro;l of Pierce universal nuclease (Thermo Fisher Scientific, 88701) was added to each sample, and the mixture was incubated for 10 min at room temperature. After sonication and streptavidin affinity purification, the precipitates were washed with a wash buffer (8 M urea in 50 mM Tris, pH 7.4). Finally, the levels of biotinylated proteins were determined by mass spectrometry in collaboration with the BioProfile (Shanghai, China).\u003c/p\u003e\n\u003ch3\u003eGST pull-down assay\u003c/h3\u003e\n\u003cp\u003eThe GST pull-down assay was performed as previously described [\u003cspan citationid=\"CR26\" class=\"CitationRef\"\u003e26\u003c/span\u003e]. Briefly, the pGEX-6P-1 plasmid encoding GST, full-length GST-NONO and fragments, full-length GST-PKM2, fragments, and mutants, as well as the pET28a plasmid encoding His-NONO and His-PKM2, were expressed in \u003cem\u003eE. coli\u003c/em\u003e BL21 and purified using glutathione S-transferase beads (GenScript, L00206) or nickel-nitrilotriacetic acid beads (GenScript, L00206) according to standard protocols. The His-PKM2 protein was mixed with purified GST, full-length GST-NONO, or fragments for 4 h at 4\u0026deg;C. Similarly, His-NONO proteins were incubated with GST, GST-PKM2 full-length or fragments or mutants at 4\u0026deg;C for 4 h. The beads were washed five times, and the results were analyzed by western blotting.\u003c/p\u003e \u003cdiv id=\"Sec11\" class=\"Section2\"\u003e \u003ch2\u003eImmunofluorescence staining\u003c/h2\u003e \u003cp\u003eThe cells were cultured overnight on glass coverslips, fixed with 4% PFA for 20 min, and permeabilized with 0.2% Triton X-100 for 20 min. After blocking with 5% BSA for 30 min, cells were incubated with primary antibodies against NONO (HUABIO, ET7108-81) and PKM2 (Proteintech, 60268-1-lg) overnight at 4\u0026deg;C, followed by incubation with fluorescence-conjugated secondary antibodies for 1 h at room temperature. The cells were then gently washed with PBS and the nuclei were stained with DAPI for 5 min at room temperature. Images were acquired using a confocal laser scanning microscope (Olympus).\u003c/p\u003e \u003c/div\u003e \u003cdiv id=\"Sec12\" class=\"Section2\"\u003e \u003ch2\u003eRNA-seq and data analysis\u003c/h2\u003e \u003cp\u003eTotal RNA was isolated from the NC, NONO-knockdown, and PKM2-knockdown MDA-MB-231 cells. RNA purification, reverse transcription, library construction, and sequencing were performed in collaboration with Majorbio Biotechnology (Shanghai, China) according to the manufacturer\u0026rsquo;s instructions (Illumina, San Diego, CA, USA). To identify differentially expressed genes (DEGs), gene expression was calculated as transcripts per million reads (TPM). A fold change\u0026thinsp;\u0026gt;\u0026thinsp;2.0, and a \u003cem\u003eP\u003c/em\u003e value\u0026thinsp;\u0026lt;\u0026thinsp;0.05 were used as the cutoff values and were considered to indicate significantly differentially expressed genes.\u003c/p\u003e \u003c/div\u003e \u003cdiv id=\"Sec13\" class=\"Section2\"\u003e \u003ch2\u003eChromatin immunoprecipitation (ChIP) assay\u003c/h2\u003e \u003cp\u003eChIP assays were performed using MDA-MB-231 cells in accordance with previously described methods [\u003cspan citationid=\"CR26\" class=\"CitationRef\"\u003e26\u003c/span\u003e]. Normal rabbit IgG (ab172730; Abcam) was used as the control. ChIP DNAs was analyzed by quantitative PCR using Rotor-Gene 6000 (Corbett Research). Primer sequences used for ChIP are listed in Additional file 2: Table S6.\u003c/p\u003e \u003c/div\u003e \u003cdiv id=\"Sec14\" class=\"Section2\"\u003e \u003ch2\u003eCUT\u0026amp;Tag\u003c/h2\u003e \u003cp\u003eCUT\u0026amp;Tag was processed according to a previously reported protocol [\u003cspan citationid=\"CR27\" class=\"CitationRef\"\u003e27\u003c/span\u003e]. This experiment was performed in MDA-MB-231 cells, and antibodies against NONO (Abcam, ab70335), H3T11ph (Active motif, 39151), and H3K27ac (Abcam, ab4729) were used in this study. DNA libraries were sequenced on an Illumina NovaSeq 6000 platform (DIATRE Biotechnology, Shanghai, China).\u003c/p\u003e \u003c/div\u003e \u003cdiv id=\"Sec15\" class=\"Section2\"\u003e \u003ch2\u003eTissue microarrays and IHC staining\u003c/h2\u003e \u003cp\u003eHuman TNBC tissue microarrays (no. TNBC1202), and clinicopathological data were obtained from Shanghai Superbiotek (Shanghai, China). IHC staining was performed according to the standard protocol of the Cell Signaling Technology. Tissue slides were incubated with primary antibodies specific for NONO (HUABIO, ET7108-81), PKM2 (Proteintech, 15822-1-AP), PAI-1 (Abcam, ab125687), and Ki-67 (Abcam, ab15580), followed by incubation with horseradish peroxidase (HRP)-conjugated secondary antibodies. The staining of NONO, PKM2, and PAI-1 in human TNBC tissues was independently assessed using a semi-quantitative H-score system by two experienced pathologists blinded to the clinical data [\u003cspan citationid=\"CR28\" class=\"CitationRef\"\u003e28\u003c/span\u003e].\u003c/p\u003e \u003c/div\u003e \u003cdiv id=\"Sec16\" class=\"Section2\"\u003e \u003ch2\u003eAnimal studies\u003c/h2\u003e \u003cp\u003eMice were maintained in a specific pathogen-free (SPF) facility on a 12 h light/dark cycle at a controlled temperature (20\u0026ndash;23\u0026deg;C) and humidity (45\u0026ndash;65%). The sample size was chosen with adequate power based on the literature and our previous experience [\u003cspan citationid=\"CR28\" class=\"CitationRef\"\u003e28\u003c/span\u003e]. For each experiment, it is indicated in the figure legend. Prior to the experiment, the mice were randomly assigned to different treatment groups. MMTV-PyMT mice on the FVB background were purchased from GemPharmatech (Nanjing, China). For NONO or PKM2 knockdown in MMTV-PyMT (FVB) mice, pAAV-U6-EGFP plasmids were transformed with shRNAs and AAVs were obtained from Syngentech (Beijing, China). AAVs were intraductally injected into the mammary glands of 5-week-old female MMTV-PyMT (FVB) mice as previously described [\u003cspan citationid=\"CR29\" class=\"CitationRef\"\u003e29\u003c/span\u003e]. After 2 weeks, tumor size was determined once a week, and tumor volumes were calculated using the following formula: volume (mm\u003csup\u003e3\u003c/sup\u003e)\u0026thinsp;=\u0026thinsp;1/2 \u0026times; length \u0026times; width\u003csup\u003e2\u003c/sup\u003e. All mice were euthanized at 12 weeks of age, and tumor and lung samples were collected, weighed, photographed, and stained with H\u0026amp;E. The Scr sequence was used as the negative control. The shRNA sequences used were as follows:\u003c/p\u003e \u003cp\u003eScr: 5\u0026rsquo;-CCTAAGGTTAAGTCGCCCTCGC-3\u0026rsquo;\u003c/p\u003e \u003cp\u003eMouse NONO shRNA-1: 5\u0026rsquo;-GCTGCAACAATGGAAGGAATT-3\u0026rsquo;\u003c/p\u003e \u003cp\u003eMouse NONO shRNA-2: 5\u0026rsquo;-ACACGAACCCTAGCGGAAATT-3\u0026rsquo;\u003c/p\u003e \u003cp\u003eMouse PKM2 shRNA-1: 5\u0026rsquo;-CTACCACTTGCAGCTATTCGA-3\u0026rsquo;\u003c/p\u003e \u003cp\u003eMouse PKM2 shRNA-1: 5\u0026rsquo;-CCACTTGCAGCTATTCGAGGA-3\u0026rsquo;\u003c/p\u003e \u003cp\u003eFor xenograft models, 6-week-old female BALB/c nude mice were purchased from GemPharmatech (Nanjing, China). MDA-MB-231 cells were infected individually with Scr, NONO-KD, or NONO-KD\u0026thinsp;+\u0026thinsp;PAI-1 lentivirus to establish stable cell lines. Subsequently, each mouse was injected subcutaneously with 5 \u0026times; 10\u003csup\u003e6\u003c/sup\u003e cells (suspended in 100 \u0026micro;l of PBS with 100 \u0026micro;l of Matrigel). Tumor size was measured every 3 days with a caliper, and the average tumor volume reached 100 mm\u003csup\u003e3\u003c/sup\u003e. After 21 days, all nude mice were sacrificed, and subcutaneous tumors were harvested, weighed, and photographed.\u003c/p\u003e \u003cp\u003eTo establish mammary-specific NONO or PKM2 knockout models in spontaneous mammary tumor mice, MMTV-Cre and NONO-floxed mice on a C57BL/6 strain background were obtained from GemPharmatech (Nanjing, China). MMTV-PyMT mice and PKM2-floxed mice on a C57BL/6 background were purchased from Jackson Laboratory (New York, USA). To obtain NONO knockout (MMTV-Cre\u003csup\u003e+/\u0026minus;\u003c/sup\u003e::MMTV-PyMT\u003csup\u003e+\u003c/sup\u003e::NONO\u003csup\u003efl/fl\u003c/sup\u003e) female mice, MMTV-Cre\u003csup\u003e+/\u0026minus;\u003c/sup\u003e::NONO\u003csup\u003efl/fl\u003c/sup\u003e female mice were crossed with the male MMTV-PyMT\u003csup\u003e+\u003c/sup\u003e::NONO\u003csup\u003efl/Y\u003c/sup\u003e mice. Female littermates (MMTV-Cre\u003csup\u003e\u0026minus;/\u0026minus;\u003c/sup\u003e::MMTV-PyMT\u003csup\u003e+\u003c/sup\u003e::NONO\u003csup\u003efl/fl\u003c/sup\u003e) were used as controls. Similarly, to obtain PKM2 knockout (MMTV-Cre\u003csup\u003e+/\u0026minus;\u003c/sup\u003e::MMTV-PyMT\u003csup\u003e+\u003c/sup\u003e::PKM2\u003csup\u003efl/fl\u003c/sup\u003e) female mice, MMTV-Cre\u003csup\u003e+/\u0026minus;\u003c/sup\u003e::PKM2\u003csup\u003efl/fl\u003c/sup\u003e female mice were crossed with MMTV-PyMT\u003csup\u003e+\u003c/sup\u003e::PKM2\u003csup\u003efl/fl\u003c/sup\u003e male mice. Female littermates (MMTV-Cre\u003csup\u003e\u0026minus;/\u0026minus;\u003c/sup\u003e::MMTV-PyMT\u003csup\u003e+\u003c/sup\u003e::PKM2\u003csup\u003efl/fl\u003c/sup\u003e) were used as controls. The overall tumor burden was measured once a week using a digital caliper beginning at week 16, and the mice were humanely euthanized at 24 weeks of age. Mammary tumors were harvested for histology, flash-frozen for protein and RNA isolation, and subjected to IHC staining with the indicated antibodies, whereas the lungs were extracted for H\u0026amp;E staining. A blinding strategy was used whenever possible when assessing outcomes. The sequences of the PCR primers used for genotyping transgenic mice are listed in Additional file 2: Table S7.\u003c/p\u003e \u003c/div\u003e \u003cdiv id=\"Sec17\" class=\"Section2\"\u003e \u003ch2\u003eStatistical analysis\u003c/h2\u003e \u003cp\u003eAll data are presented as mean\u0026thinsp;\u0026plusmn;\u0026thinsp;SD unless otherwise indicated. GraphPad Prism software (version 7.0) was used to assess significant differences between groups. Comparisons between two groups were performed using an unpaired two-tailed Student\u0026rsquo;s t-test. Multiple comparisons were performed using a one-way analysis of variance (ANOVA). \u003cem\u003eP\u003c/em\u003e\u0026thinsp;\u0026lt;\u0026thinsp;0.05. One, two, three, and four asterisks indicate \u003cem\u003eP\u003c/em\u003e\u0026thinsp;\u0026lt;\u0026thinsp;0.05, \u003cem\u003eP\u003c/em\u003e\u0026thinsp;\u0026lt;\u0026thinsp;0.01, \u003cem\u003eP\u003c/em\u003e\u0026thinsp;\u0026lt;\u0026thinsp;0.001, and \u003cem\u003eP\u003c/em\u003e\u0026thinsp;\u0026lt;\u0026thinsp;0.0001, respectively.\u003c/p\u003e \u003c/div\u003e"},{"header":"Results","content":"\u003cdiv id=\"Sec19\" class=\"Section2\"\u003e \u003ch2\u003eNONO directly interacts with nuclear PKM2 in TNBC cells\u003c/h2\u003e \u003cp\u003eThe paraspeckle protein NONO plays a critical role in TNBC, although its direct downstream transcriptional target genes are unknown [\u003cspan additionalcitationids=\"CR14\" citationid=\"CR13\" class=\"CitationRef\"\u003e13\u003c/span\u003e\u0026ndash;\u003cspan citationid=\"CR15\" class=\"CitationRef\"\u003e15\u003c/span\u003e]. To identify potential proteins that interact with NONO, we used a proximity-dependent biotinylation identification approach known as BioID2 [\u003cspan citationid=\"CR25\" class=\"CitationRef\"\u003e25\u003c/span\u003e], in which NONO is fused to the N-terminus of the BioID2 vector and transduced into human MDA-MB-231 cells. An empty vector containing only BirA biotin ligase was used as the control. After biotin-streptavidin affinity purification, proteins associated with NONO were analyzed using quantitative mass spectrometry. Among the proteins that were specifically enriched in NONO-BioID2-expressing cells, PKM2 was identified as an NONO-interacting protein in the top 10 list (Fig.\u0026nbsp;\u003cspan refid=\"Fig1\" class=\"InternalRef\"\u003e1\u003c/span\u003eA, Additional file 2: Table \u003cspan refid=\"MOESM1\" class=\"InternalRef\"\u003eS1\u003c/span\u003e). In addition, we found that SFPQ, PSPC1, and MSN [\u003cspan additionalcitationids=\"CR13\" citationid=\"CR12\" class=\"CitationRef\"\u003e12\u003c/span\u003e\u0026ndash;\u003cspan citationid=\"CR14\" class=\"CitationRef\"\u003e14\u003c/span\u003e], which are NONO-binding proteins, are also present. To confirm the interaction between NONO and PKM2, we performed co-immunoprecipitation (co-IP) experiments and found that NONO interacted with PKM2 in both MDA-MB-231 and BT-549 cells (Fig.\u0026nbsp;\u003cspan refid=\"Fig1\" class=\"InternalRef\"\u003e1\u003c/span\u003eB and C). Furthermore, immunofluorescence staining revealed that NONO co-localized with PKM2 in the nuclei of MDA-MB-231 cells (Fig.\u0026nbsp;\u003cspan refid=\"Fig1\" class=\"InternalRef\"\u003e1\u003c/span\u003eD). These results agree with previous observations that PKM2 is present in the nucleus [\u003cspan citationid=\"CR20\" class=\"CitationRef\"\u003e20\u003c/span\u003e, \u003cspan citationid=\"CR21\" class=\"CitationRef\"\u003e21\u003c/span\u003e, \u003cspan citationid=\"CR30\" class=\"CitationRef\"\u003e30\u003c/span\u003e].\u003c/p\u003e \u003cp\u003eNext, we found that NONO directly interacted with PKM2 in the GST pull-down experiments (Fig.\u0026nbsp;\u003cspan refid=\"Fig1\" class=\"InternalRef\"\u003e1\u003c/span\u003eE). To further characterize the determinants mediating the association between NONO and PKM2, we mapped NONO protein domains using GST pull-down experiments and demonstrated that the NOPS and coiled-coil domains of NONO were sufficient for their interaction (Fig.\u0026nbsp;\u003cspan refid=\"Fig1\" class=\"InternalRef\"\u003e1\u003c/span\u003eF). Similarly, we demonstrated that the A and C domains of PKM2 were responsible for its interaction with NONO (Fig.\u0026nbsp;\u003cspan refid=\"Fig1\" class=\"InternalRef\"\u003e1\u003c/span\u003eG), indicating that NONO interacts with PKM2 through multiple domains. Taken together, these data indicate that PKM2 is a novel protein that interacts with NONO in the TNBC cell nuclei.\u003c/p\u003e \u003cp\u003e \u003cb\u003eNONO expression is associated with the prognosis of TNBC patients, and NONO is required for TNBC cell metastasis\u003c/b\u003e \u003c/p\u003e \u003cp\u003eTo investigate the clinical significance of NONO expression in patients with TNBC, we first analyzed NONO expression by immunohistochemistry (IHC) using tissue microarrays containing 60 TNBC samples and matched adjacent normal tissues. We observed that NONO expression was significantly upregulated in TNBC tissues compared to that in the adjacent normal tissues (Fig.\u0026nbsp;\u003cspan refid=\"Fig2\" class=\"InternalRef\"\u003e2\u003c/span\u003eA and B). Notably, NONO expression correlated with tumor size and higher-grade lymph node status in patients with TNBC (Fig.\u0026nbsp;\u003cspan refid=\"Fig2\" class=\"InternalRef\"\u003e2\u003c/span\u003eC; Additional file 2: Table S2). Importantly, Kaplan-Meier survival analysis revealed that TNBC patients with high NONO expression had a shorter overall survival (Fig.\u0026nbsp;\u003cspan refid=\"Fig2\" class=\"InternalRef\"\u003e2\u003c/span\u003eD). The expression levels of NONO in TNBC tissues were significantly higher than those in non-TNBC tissues (Additional file 1: Fig. \u003cspan refid=\"MOESM1\" class=\"InternalRef\"\u003eS1\u003c/span\u003eA). These results indicate that NONO is upregulated in human TNBC tissues and correlates with poor prognosis in patients with TNBC, suggesting that NONO may promote cancer cell invasion during malignant progression.\u003c/p\u003e \u003cp\u003eTo determine the effect of NONO on cell growth and invasion, two independent short hairpin RNAs (shRNAs) targeting NONO were used to silence NONO expression. The knockdown efficiency of NONO in human MDA-MB-231 and BT-549 TNBC cell lines was determined by western blot analysis (Fig.\u0026nbsp;\u003cspan refid=\"Fig2\" class=\"InternalRef\"\u003e2\u003c/span\u003eE). CCK-8 and colony formation assays indicated that the proliferation of MDA-MB-231 and BT-549 cells was significantly inhibited upon NONO knockdown compared with that of scrambled control (Scr) cells (Fig.\u0026nbsp;\u003cspan refid=\"Fig2\" class=\"InternalRef\"\u003e2\u003c/span\u003eF and G). Transwell assays revealed that the migratory and invasive abilities of TNBC cells were significantly lower in the NONO knockdown group than in the Scr group (Fig.\u0026nbsp;\u003cspan refid=\"Fig2\" class=\"InternalRef\"\u003e2\u003c/span\u003eH). In addition, the well-established MMTV-PyMT (FVB background) transgenic murine model of spontaneous mammary tumors [\u003cspan citationid=\"CR31\" class=\"CitationRef\"\u003e31\u003c/span\u003e] was used to determine whether NONO directly regulated tumorigenesis. Remarkably, adeno-associated virus (AAV)-mediated NONO depletion in mouse breast tissue was sufficient to attenuate tumor growth (Fig.\u0026nbsp;\u003cspan refid=\"Fig2\" class=\"InternalRef\"\u003e2\u003c/span\u003eI, J, and K). More importantly, NONO depletion substantially reduced the number of metastatic lung nodules (Fig.\u0026nbsp;\u003cspan refid=\"Fig2\" class=\"InternalRef\"\u003e2\u003c/span\u003eL and M). These results indicated that NONO is crucial for TNBC growth and metastasis.\u003c/p\u003e \u003c/div\u003e \u003cdiv id=\"Sec20\" class=\"Section2\"\u003e \u003ch2\u003ePKM2 expression is upregulated in TNBC, and knockdown of PKM2 inhibits TNBC cell metastasis\u003c/h2\u003e \u003cp\u003eSimilarly, we investigated the clinical significance of PKM2 expression in TNBC patients and found that PKM2 expression was upregulated in human TNBC tissues and correlated with poor prognosis in TNBC patients (Fig.\u0026nbsp;\u003cspan refid=\"Fig3\" class=\"InternalRef\"\u003e3\u003c/span\u003eA, B, and C; Additional file 1: Fig. \u003cspan refid=\"MOESM1\" class=\"InternalRef\"\u003eS1\u003c/span\u003eB and Table S3), which is consistent with previous results [\u003cspan citationid=\"CR30\" class=\"CitationRef\"\u003e30\u003c/span\u003e] and further suggests that PKM2 may promote cancer cell invasion during malignant progression. Furthermore, our \u003cem\u003ein vitro\u003c/em\u003e knockdown experiments (Fig.\u0026nbsp;\u003cspan refid=\"Fig3\" class=\"InternalRef\"\u003e3\u003c/span\u003eD, E, F, and G) and \u003cem\u003ein vivo\u003c/em\u003e animal study results (Fig.\u0026nbsp;\u003cspan refid=\"Fig3\" class=\"InternalRef\"\u003e3\u003c/span\u003eH, I, J, K, and L) indicated that PKM2 is crucial for TNBC growth and metastasis.\u003c/p\u003e \u003cp\u003e \u003cb\u003eSERPINE1\u003c/b\u003e \u003cb\u003eis a key transcriptional target of NONO and PKM2 in TNBC cells\u003c/b\u003e\u003c/p\u003e \u003cp\u003eNext, we sought to understand how NONO and PKM2 regulate the migration and invasion of TNBC cells. To identify potential transcriptional targets of the NONO/PKM2 complex, we performed RNA-seq analysis to profile co-regulated target genes. Through integrated analysis of RNA-seq results following NONO and PKM2 knockdown in MDA-MB-231 cells, we found that nearly half of the differentially expressed genes DEGs (451/999) following NONO knockdown were also regulated by PKM2 (Fig.\u0026nbsp;\u003cspan refid=\"Fig4\" class=\"InternalRef\"\u003e4\u003c/span\u003eA, GSE266177). Further analysis revealed that \u003cem\u003eSERPINE1\u003c/em\u003e (encoding the PAI-1 protein) [\u003cspan citationid=\"CR22\" class=\"CitationRef\"\u003e22\u003c/span\u003e, \u003cspan citationid=\"CR23\" class=\"CitationRef\"\u003e23\u003c/span\u003e, \u003cspan citationid=\"CR32\" class=\"CitationRef\"\u003e32\u003c/span\u003e] was the gene whose expression was most downregulated by either NONO or PKM2 knockdown (Fig.\u0026nbsp;\u003cspan refid=\"Fig4\" class=\"InternalRef\"\u003e4\u003c/span\u003eB, GSE266177). In the top 10 heatmaps, IL11, CCN2, RCN1, VDAC1, CDKN1A (P21), ADAMTSL4, MATN2, FERMT2, and MCAM, which play key roles in cell growth, adhesion, migration, and differentiation [\u003cspan additionalcitationids=\"CR34 CR35 CR36 CR37 CR38 CR39\" citationid=\"CR33\" class=\"CitationRef\"\u003e33\u003c/span\u003e\u0026ndash;\u003cspan citationid=\"CR40\" class=\"CitationRef\"\u003e40\u003c/span\u003e], were significantly downregulated when either NONO or PKM2 was knocked down. Given that PAI-1 facilitates tumor cell detachment from the matrix and promotes tumor dissemination and metastasis, which has been recommended as a promising biomarker for poor prognosis in primary breast cancer patients by the American Society of Clinical Oncology (ASCO) and the European Organization for Research and Treatment of Cancer (EORTC) clinical operation guidelines [\u003cspan citationid=\"CR22\" class=\"CitationRef\"\u003e22\u003c/span\u003e, \u003cspan citationid=\"CR23\" class=\"CitationRef\"\u003e23\u003c/span\u003e], we selected \u003cem\u003eSERPINE1\u003c/em\u003e as a primary target for further study. We confirmed that NONO knockdown in MDA-MB-231 cells significantly reduced the expression of \u003cem\u003eSERPINE1\u003c/em\u003e at both the transcriptional and protein level (Fig.\u0026nbsp;\u003cspan refid=\"Fig4\" class=\"InternalRef\"\u003e4\u003c/span\u003eC and D). Subsequently, we examined whether the enforced expression of PAI-1 would compensate for NONO knockdown. We first overexpressed exogenous PAI-1 in NONO-depleted MAD-MB-231 cells (Fig.\u0026nbsp;\u003cspan refid=\"Fig4\" class=\"InternalRef\"\u003e4\u003c/span\u003eE). We then performed CCK-8, colony formation, and Transwell assays using these cells. We found that the overexpression of PAI-1 significantly rescued the reduced proliferation, migration, and invasion of NONO-depleted cells (Fig.\u0026nbsp;\u003cspan refid=\"Fig4\" class=\"InternalRef\"\u003e4\u003c/span\u003eF, G, and H). To further support the \u003cem\u003ein vitro\u003c/em\u003e results, we performed \u003cem\u003ein vivo\u003c/em\u003e analysis using xenograft models in nude mice. We showed that overexpression of PAI-1 significantly reversed the growth defects in NONO-depleted MDA-MB-231 xenograft tumors (Fig.\u0026nbsp;\u003cspan refid=\"Fig4\" class=\"InternalRef\"\u003e4\u003c/span\u003eI, J, and K).\u003c/p\u003e \u003cp\u003eSimilarly, we found that knockdown of PKM2 significantly reduced \u003cem\u003eSERPINE1\u003c/em\u003e transcription in MDA-MB-231 cells (Fig.\u0026nbsp;\u003cspan refid=\"Fig4\" class=\"InternalRef\"\u003e4\u003c/span\u003eL and M). The proliferative, migratory, and invasive capabilities of PKM2-depleted MDA-MB-231 cells could be rescued by ectopic expression of PAI-1 (Fig.\u0026nbsp;\u003cspan refid=\"Fig4\" class=\"InternalRef\"\u003e4\u003c/span\u003eN, O, P, and Q). Consistent experimental results were obtained regarding the roles of NONO and PKM2 in human BT-549 TNBC cells (Additional file 1: Fig. S2A-L).\u003c/p\u003e \u003cp\u003eTo further investigate the clinical relevance of PAI-1 expression in patients with TNBC, we examined its expression using IHC on tissue microarrays containing 60 pairs of TNBC samples and their matched adjacent normal tissues. We demonstrated that PAI-1 was notably upregulated in TNBC tissues compared to adjacent normal tissues (Additional file 1: Fig. S2M and N). Importantly, the expression levels of NONO and PAI-1, as well as those of PKM2 and PAI-1, were significantly positively correlated in human TNBC samples according to Pearson correlation analysis (Fig.\u0026nbsp;\u003cspan refid=\"Fig4\" class=\"InternalRef\"\u003e4\u003c/span\u003eR), further confirming that \u003cem\u003eSERPINE1\u003c/em\u003e is the downstream target gene of NONO/PKM2 in TNBC cells. Collectively, these data suggest that NONO/PKM2 promotes TNBC progression by activating \u003cem\u003eSERPINE1\u003c/em\u003e transcription.\u003c/p\u003e \u003cp\u003e \u003cb\u003eNONO-dependent PKM2 and its nuclear protein kinase activity are critical for\u003c/b\u003e \u003cb\u003eSERPINE1\u003c/b\u003e \u003cb\u003etranscription and TNBC progression\u003c/b\u003e\u003c/p\u003e \u003cp\u003eGiven that NONO and PKM2 positively regulate \u003cem\u003eSERPINE1\u003c/em\u003e transcription in TNBC cells, and that they directly interact in the nucleus, we investigated how they regulate \u003cem\u003eSERPINE1\u003c/em\u003e expression. As expected, enforced the overexpression of PKM2 enhanced \u003cem\u003eSERPINE1\u003c/em\u003e expression. However, this increase in expression was abolished by NONO knockdown (Fig.\u0026nbsp;\u003cspan refid=\"Fig5\" class=\"InternalRef\"\u003e5\u003c/span\u003eA and B). Next, we examined whether PKM2-mediated H3T11ph modifications at the \u003cem\u003eSERPINE1\u003c/em\u003e promoter were enriched in a NONO-dependent manner. ChIP‒qPCR revealed a significant reduction in H3T11ph enrichment at the \u003cem\u003eSERPINE1\u003c/em\u003e promoter in the NONO knockdown group compared to that in the negative control (NC) group (Fig.\u0026nbsp;\u003cspan refid=\"Fig5\" class=\"InternalRef\"\u003e5\u003c/span\u003eC). Previous studies have demonstrated that PKM2 exhibits pyruvate kinase or protein kinase activity, which depends on its cytosolic tetramer or nuclear dimer state [\u003cspan citationid=\"CR19\" class=\"CitationRef\"\u003e19\u003c/span\u003e, \u003cspan citationid=\"CR41\" class=\"CitationRef\"\u003e41\u003c/span\u003e, \u003cspan citationid=\"CR42\" class=\"CitationRef\"\u003e42\u003c/span\u003e]. To further explore whether the protein kinase of PKM2 is crucial for \u003cem\u003eSERPINE1\u003c/em\u003e transcriptional activation, we utilized two well-established PKM2 mutants, PKM2-Y105F (predominant tetramer form harboring pyruvate kinase activity) [\u003cspan citationid=\"CR42\" class=\"CitationRef\"\u003e42\u003c/span\u003e] and PKM2-R399E (predominant dimer form harboring protein kinase activity) [\u003cspan citationid=\"CR19\" class=\"CitationRef\"\u003e19\u003c/span\u003e] to examine their effects on \u003cem\u003eSERPINE1\u003c/em\u003e expression. We overexpressed PKM2-WT, PKM2-Y105F, or PKM2-R399E in PKM2-depleted MDA-MB-231 cells. We found that the PKM2-Y105F mutant did not activate \u003cem\u003eSERPINE1\u003c/em\u003e expression, whereas the PKM2-R399E mutant had an activating effect on \u003cem\u003eSERPINE1\u003c/em\u003e expression similar to that of PKM2-WT (Fig.\u0026nbsp;\u003cspan refid=\"Fig6\" class=\"InternalRef\"\u003e6\u003c/span\u003eD and E). These results suggest that the protein kinase activity of PKM2 is key to activating \u003cem\u003eSERPINE1\u003c/em\u003e expression in the nucleus.\u003c/p\u003e \u003cp\u003eTo identify the potential key residues of PKM2 responsible for NONO interactions, we used the ZDOCK server (\u003cspan class=\"ExternalRef\"\u003e\u003cspan class=\"RefSource\"\u003ehttps://zdock.umassmed.edu/\u003c/span\u003e\u003cspan address=\"https://zdock.umassmed.edu/\" targettype=\"URL\" class=\"RefTarget\"\u003e\u003c/span\u003e\u003c/span\u003e) for molecular docking analyses. Molecular docking confirmed good and stable binding of NONO to PKM2 (Additional file 1: Fig. S3A) and revealed seven positions of PKM2 that may play important roles in the interaction between PKM2 and NONO (Additional file 1: Fig. S3B). GST pull-down assays demonstrated that the PKM2-S406A mutant (Ser to Ala at aa 406) significantly reduced this interaction, whereas the interactions of PKM2-R400A, T412A, D476A, D487A, W515A, and R526A mutants with NONO were similar to those of wild-type PKM2 (PKM2-WT, Fig.\u0026nbsp;\u003cspan refid=\"Fig5\" class=\"InternalRef\"\u003e5\u003c/span\u003eF). To explore the effect of the S406A mutation of PKM2 on TNBC progression, we overexpressed PKM2-WT or the PKM2-S406A mutant in MDA-MB-231 cells. Consistently, the PKM2-S406A mutant immunoprecipitated significantly less NONO in the MDA-MB-231 cells (Fig.\u0026nbsp;\u003cspan refid=\"Fig5\" class=\"InternalRef\"\u003e5\u003c/span\u003eG). Notably, the PKM2-S406A mutant exhibited the same subcellular distribution as that of PKM2-WT (Fig.\u0026nbsp;\u003cspan refid=\"Fig5\" class=\"InternalRef\"\u003e5\u003c/span\u003eH). However, compared with PKM2-WT, PKM2-S406A overexpression in MDA-MB-231 cells failed to activate \u003cem\u003eSERPINE1\u003c/em\u003e expression (Fig.\u0026nbsp;\u003cspan refid=\"Fig5\" class=\"InternalRef\"\u003e5\u003c/span\u003eI and J). In addition, we found that compared to PKM2-WT, PKM2-S406A overexpression in MDA-MB-231 cells significantly inhibited cell growth, migration, and invasion (Fig.\u0026nbsp;\u003cspan refid=\"Fig5\" class=\"InternalRef\"\u003e5\u003c/span\u003eK, L, and M). Taken together, these results demonstrated that NONO-dependent PKM2 and its nuclear protein kinase activity are crucial for \u003cem\u003eSERPINE1\u003c/em\u003e expression and TNBC cell invasion.\u003c/p\u003e \u003cp\u003e \u003cb\u003ePKM2-mediated H3T11ph cooperates with TIP60-mediated H3K27ac to promote\u003c/b\u003e \u003cb\u003eSERPINE1\u003c/b\u003e \u003cb\u003eexpression\u003c/b\u003e\u003c/p\u003e \u003cp\u003eA previous study has revealed that PKM2 mediates H3T11ph, which is involved in transcriptional regulation [\u003cspan citationid=\"CR21\" class=\"CitationRef\"\u003e21\u003c/span\u003e]. To explore the effect of PKM2 on other histone modifications, we examined global changes in other key histone H3 modifications upon PKM2 knockdown in MDA-MB-231 cells. As expected, the levels of H3T11ph were markedly decreased upon PKM2 knockdown (Fig.\u0026nbsp;\u003cspan refid=\"Fig6\" class=\"InternalRef\"\u003e6\u003c/span\u003eA). Interestingly, we found that the levels of H3K27ac, a promoter and enhancer marker [\u003cspan additionalcitationids=\"CR44\" citationid=\"CR43\" class=\"CitationRef\"\u003e43\u003c/span\u003e\u0026ndash;\u003cspan citationid=\"CR45\" class=\"CitationRef\"\u003e45\u003c/span\u003e], were markedly lower in PKM2-knockdown cells than in NC cells (Fig.\u0026nbsp;\u003cspan refid=\"Fig6\" class=\"InternalRef\"\u003e6\u003c/span\u003eA). Additionally, we observed that the levels of the histone markers H3K4me1 and H3K9ac, which have been previously described [\u003cspan citationid=\"CR21\" class=\"CitationRef\"\u003e21\u003c/span\u003e], decreased upon PKM2 knockdown (Fig.\u0026nbsp;\u003cspan refid=\"Fig6\" class=\"InternalRef\"\u003e6\u003c/span\u003eA). There were no obvious changes in the levels of H3T3ph, H3K4me2/3, H3K4ac, H3K9me3, H3S10ph, H3K14ac, H3K14la, H3R17me2s, H3K18ac, or H3K27me2/3 modifications between PKM2 knockdown cells and NC cells (Fig.\u0026nbsp;\u003cspan refid=\"Fig6\" class=\"InternalRef\"\u003e6\u003c/span\u003eA). These data suggested that PKM2-mediated H3T11ph cooperates with H3K27ac to regulate gene transcription in TNBC cells.\u003c/p\u003e \u003cp\u003eTo understand how NONO, H3T11ph, and H3K27ac collaborate to regulate gene transcription, we performed cleavage under targets and tagmentation (CUT\u0026amp;Tag) experiments in MDA-MB-231 cells to determine the enrichment profiles of NONO, H3T11ph, and H3K27ac in the whole genome. Interestingly, we found that NONO, H3T11ph, and H3K27ac signals were significantly enriched at transcription start sites (TSSs), implying that they may perform transcriptional regulatory functions (Fig.\u0026nbsp;\u003cspan refid=\"Fig6\" class=\"InternalRef\"\u003e6\u003c/span\u003eB, GSE266179). In addition, H3T11ph and H3K27ac signals were markedly reduced in PKM2-KD cells compared to their respective NC cells (Fig.\u0026nbsp;\u003cspan refid=\"Fig6\" class=\"InternalRef\"\u003e6\u003c/span\u003eB), which was in good agreement with our western blot analysis results (Fig.\u0026nbsp;\u003cspan refid=\"Fig6\" class=\"InternalRef\"\u003e6\u003c/span\u003eA). In fact, we found that NONO, H3T11ph, and H3K27ac were co-enriched in the promoter, TSS, and 3\u0026rsquo;-end regions of \u003cem\u003eSERPINE1\u003c/em\u003e (Fig.\u0026nbsp;\u003cspan refid=\"Fig6\" class=\"InternalRef\"\u003e6\u003c/span\u003eC). These results were further confirmed by ChIP‒qPCR in MDA-MB-231 cells (Fig.\u0026nbsp;\u003cspan refid=\"Fig6\" class=\"InternalRef\"\u003e6\u003c/span\u003eD). Notably, NONO enrichment largely overlapped with H3T11ph peaks genome-wide in MDA-MB-231 cells (Additional file 1: Fig. S4A, GSE266179). Moreover, through bioinformatics analysis, we found that the genome-wide occupancy of NONO and H3T11ph, H3T11ph, and H3K27ac was highly correlated, although there was no significant correlation between NONO and H3K27ac (Additional file 1: Fig. S4B). These results further suggest that PKM2-mediated H3T11ph could be enriched in promoters through NONO recruitment of PKM2, where H3T11ph cooperates with H3K27ac to activate \u003cem\u003eSERPINE1\u003c/em\u003e transcription.\u003c/p\u003e \u003cp\u003eNext, we explored the possible link between H3T11ph and H3K27ac. We searched the RNA-seq data obtained upon PKM2 knockdown (GSE266177) and examined changes in the expression levels of histone acetyltransferases \u003cem\u003eKAT5\u003c/em\u003e (encoding TIP60), \u003cem\u003eKAT3B\u003c/em\u003e (encoding PCAF), \u003cem\u003eCREBBP\u003c/em\u003e (encoding CBP), and \u003cem\u003eEP300\u003c/em\u003e (encoding P300), which are associated with histone acetylation. We then performed western blot analyses and found that PKM2 knockdown significantly reduced the expression of TIP60 but upregulated P300 expression in MDA-MB-231 cells, whereas the expression of PCAF and CBP remained unchanged compared with that in NC controls (Additional file 1: Fig. S5A). Therefore, we selected KAT5/TIP60 for further study. RT-qPCR assays confirmed that \u003cem\u003eKAT5\u003c/em\u003e mRNA levels significantly decreased following PKM2 knockdown (Additional file 1: Fig. S5B). Similar results were obtained for the BT-549 cells (Additional file 1: Fig. S6A and B). In addition, our CUT\u0026amp;Tag data demonstrated that H3T11ph modifications were enriched in the \u003cem\u003eKAT5\u003c/em\u003e promoter and that H3T11ph enrichment was significantly reduced in the promoter upon PKM2 knockdown (Additional file 1: Fig. S5C). Consistent results were obtained by ChIP‒qPCR in MDA-MB-231 cells (Additional file 1: Fig. S5D). These data indicated that PKM2 directly activates \u003cem\u003eKAT5\u003c/em\u003e transcription.\u003c/p\u003e \u003cp\u003eTo determine whether TIP60 regulates \u003cem\u003eSERPINE1\u003c/em\u003e expression, we knocked down \u003cem\u003eKAT5\u003c/em\u003e expression in MDA-MB-231 cells. \u003cem\u003eKAT5\u003c/em\u003e knockdown significantly reduced \u003cem\u003eSERPINE1\u003c/em\u003e expression in MDA-MB-231 cells compared to that in NC control cells (Additional file 1: Fig. S5E and F). As expected, the levels of H3K27ac were markedly reduced following \u003cem\u003eKAT5\u003c/em\u003e knockdown (Additional file 1: Fig. S5F). Importantly, the levels of PAI-1 and H3K27ac in PKM2-depleted MDA-MB-231 cells were partially restored by ectopic TIP60 expression (Additional file 1: Fig. S5G). These results were also observed in BT-549 cells (Additional file 1: Fig. S6C, D and E). In addition, we analyzed the expression profiles extracted from GEO datasets (GSE76275) and found that the expression of \u003cem\u003ePKM2\u003c/em\u003e and \u003cem\u003eKAT5\u003c/em\u003e was positively correlated in human TNBC samples (Additional file 1: Fig. S6F). Taken together, these results suggest that PKM2 can also transcriptionally regulate \u003cem\u003eKAT5\u003c/em\u003e expression and that TIP60-mediated H3K27ac cooperates with PKM2-mediated H3T11ph to activate \u003cem\u003eSERPINE1\u003c/em\u003e expression.\u003c/p\u003e \u003cp\u003e \u003cb\u003eNONO or PKM2 deficiency reduces PAI-1 expression and inhibits the malignant progression of spontaneous mammary tumors in mice\u003c/b\u003e \u003c/p\u003e \u003cp\u003eThe nuclear protein NONO is highly conserved in humans and mice, and shares 98% amino acid sequence similarity [\u003cspan citationid=\"CR7\" class=\"CitationRef\"\u003e7\u003c/span\u003e, \u003cspan citationid=\"CR8\" class=\"CitationRef\"\u003e8\u003c/span\u003e]. To further assess the role of NONO in regulating mammary tumor progression \u003cem\u003ein vivo\u003c/em\u003e, we constructed a spontaneous mammary tumor mouse line in which NONO was specifically knocked out in the breast tissue (Fig.\u0026nbsp;\u003cspan refid=\"Fig7\" class=\"InternalRef\"\u003e7\u003c/span\u003eA). Consistent with our previous results, conditional loss of NONO in mammary tissue significantly inhibited tumor growth (Fig.\u0026nbsp;\u003cspan refid=\"Fig7\" class=\"InternalRef\"\u003e7\u003c/span\u003eB and C; Additional file 1: Fig. S7A). In addition, knockout of NONO markedly reduced the lung metastatic capacity and suppressed the formation of larger metastatic nodules in spontaneous mammary tumor model mice (Fig.\u0026nbsp;\u003cspan refid=\"Fig7\" class=\"InternalRef\"\u003e7\u003c/span\u003eD). The intratumoral levels of NONO, PAI-1, and Ki67 were analyzed using western blotting and immunohistochemical (IHC) staining. Conditional mammary NONO depletion significantly reduced PAI-1 and Ki67 expression (Fig.\u0026nbsp;\u003cspan refid=\"Fig7\" class=\"InternalRef\"\u003e7\u003c/span\u003eE and F; Additional file 1: Fig. S7B).\u003c/p\u003e \u003cp\u003eWe also generated a mouse model of spontaneous breast cancer with mammary-specific PKM2 knockout (Fig.\u0026nbsp;\u003cspan refid=\"Fig7\" class=\"InternalRef\"\u003e7\u003c/span\u003eG). Similarly, tumor growth and lung metastatic capacity were significantly inhibited by conditional PKM2 knockout in breast tissue (Fig.\u0026nbsp;\u003cspan refid=\"Fig7\" class=\"InternalRef\"\u003e7\u003c/span\u003eH, I, and J; Additional file 1: Fig. S7C). The intratumoral levels of PKM2, PAI-1, and Ki67 were analyzed using western blotting and immunohistochemical (IHC) staining. Conditional mammary PKM2 depletion significantly reduced PAI-1 and Ki67 expression (Fig.\u0026nbsp;\u003cspan refid=\"Fig7\" class=\"InternalRef\"\u003e7\u003c/span\u003eK and L; Additional file 1: Fig. S7D). Taken together, these \u003cem\u003ein vivo\u003c/em\u003e data reinforce the notion that NONO and PKM2 are critical for the malignant progression of breast tumors via \u003cem\u003eSERPINE1\u003c/em\u003e transcriptional activation.\u003c/p\u003e \u003c/div\u003e"},{"header":"Discussion","content":"\u003cp\u003eThe prognosis of patients with TNBC remains poor because of the lack of specific biomarkers for effective interventions [\u003cspan citationid=\"CR2\" class=\"CitationRef\"\u003e2\u003c/span\u003e, \u003cspan citationid=\"CR46\" class=\"CitationRef\"\u003e46\u003c/span\u003e]. Therefore, elucidating novel molecular mechanisms and developing effective therapeutic targets for TNBC is highly important. In this study, we found that NONO specifically interacts with nuclear PKM2 to transcriptionally activate \u003cem\u003eSERPINE1\u003c/em\u003e expression and promote TNBC cell metastasis. In addition, we found that PKM2-mediated H3T11ph cooperates with TIP60-mediated H3K27ac to regulate gene transcription in an NONO-dependent manner. These results revealed a novel mechanism by which PKM2, a protein kinase, directly regulates gene transcription and promotes TNBC metastasis.\u003c/p\u003e \u003cp\u003eAs a multifunctional nuclear protein, NONO has diverse functions in tumorigenesis, through which it may interact with distinct protein partners [\u003cspan citationid=\"CR12\" class=\"CitationRef\"\u003e12\u003c/span\u003e]. Previous studies have shown that NONO interacts with the Hippo pathway effector TAZ to undergo liquid\u0026ndash;liquid phase separation, which promotes TAZ-mediated oncogenic transcription [\u003cspan citationid=\"CR47\" class=\"CitationRef\"\u003e47\u003c/span\u003e]. In addition, a recent study demonstrated that NONO is important for transactivation of EGFR by stabilizing nuclear EGFR expression and recruiting other transcriptional coactivators [\u003cspan citationid=\"CR14\" class=\"CitationRef\"\u003e14\u003c/span\u003e]. However, how the NONO-driven transcriptional program facilitates malignant development of cancer remains unclear. In this study, we found that PKM2 directly interacted with NONO and executed its protein kinase function to facilitate TNBC metastasis. Our data showed that NONO enrichment was strongly correlated with nuclear PKM2-mediated H3T11ph marks along genomic loci, including \u003cem\u003eSERPINE1\u003c/em\u003e. Interestingly, we observed that approximately 45% of the NONO-targeting genes were also regulated by PKM2 in TNBC cells. These findings suggested that nuclear PKM2 is important for NONO-mediated gene expression in TNBC cells.\u003c/p\u003e \u003cp\u003eIn addition to its glycolytic function, PKM2 has non-metabolic functions that are critical for gene expression. Within the nucleus, PKM2 is a transcriptional coactivator that confers malignant potential to cancer cells through its association with various transcription factors including Oct-4, HIF-1α, β-catenin, and STAT3 [\u003cspan citationid=\"CR19\" class=\"CitationRef\"\u003e19\u003c/span\u003e, \u003cspan citationid=\"CR20\" class=\"CitationRef\"\u003e20\u003c/span\u003e, \u003cspan citationid=\"CR48\" class=\"CitationRef\"\u003e48\u003c/span\u003e, \u003cspan citationid=\"CR49\" class=\"CitationRef\"\u003e49\u003c/span\u003e]. However, the regulatory processes associated with non-metabolic PKM2 involve non-histone phosphorylation (H3T11ph)-mediated transcription of downstream target genes. Intriguingly, upon EGF receptor activation, PKM2 binds histone H3 and phosphorylates histone H3 at T11, resulting in the acetylation of histone H3 at K9 to activate CCND1 and MYC expression in glioblastoma cells [\u003cspan citationid=\"CR21\" class=\"CitationRef\"\u003e21\u003c/span\u003e]. In addition, a recent study reported that PKM2 interacts with the histone methyltransferase EZH2 to regulate the metabolic switch from glycolysis to fatty acid βoxidation in TNBC [\u003cspan citationid=\"CR30\" class=\"CitationRef\"\u003e30\u003c/span\u003e]. However, there was no indication of how PKM2/EZH2 was recruited to the target genes in this study [\u003cspan citationid=\"CR30\" class=\"CitationRef\"\u003e30\u003c/span\u003e]. In contrast, we did not observe any change in H3K27me3 levels upon PKM2 knockdown compared with the NC control in MDA-MB-231 cells in our study. This discrepancy could be due to different cell sources and manipulations. Interestingly, in the current study, we found that PKM2 phosphorylated histone H3 at T11 in a NONO-dependent manner, and this phosphorylation coincided with the acetylation of histone H3 at K27 to activate \u003cem\u003eSERPINE1\u003c/em\u003e expression in TNBC. These results revealed more precise genome-wide enrichment of PKM2-mediated H3T11ph and demonstrated a novel crosslink between histone marks. H3K27ac is an active enhancer mark [\u003cspan additionalcitationids=\"CR44\" citationid=\"CR43\" class=\"CitationRef\"\u003e43\u003c/span\u003e\u0026ndash;\u003cspan citationid=\"CR45\" class=\"CitationRef\"\u003e45\u003c/span\u003e]. Thus, our data suggests that PKM2-mediated H3T11ph may also be associated with active enhancers. NONO can bind to enhancer regions in human glioblastoma cells and mouse retina [\u003cspan citationid=\"CR47\" class=\"CitationRef\"\u003e47\u003c/span\u003e, \u003cspan citationid=\"CR50\" class=\"CitationRef\"\u003e50\u003c/span\u003e]. Therefore, the mechanism by which PKM2-mediated H3T11ph modification is linked to the NONO-mediated regulation of enhancer activity warrants further investigation. Nevertheless, the specific role of PKM2 makes it an attractive therapeutic target in cancer treatment. However, the complexity of PKM2 regulation and signaling has led researchers to face the following dilemma: whether to use PKM2 activators or inhibitors for cancer treatment [\u003cspan citationid=\"CR17\" class=\"CitationRef\"\u003e17\u003c/span\u003e]. The current study provides an alternative intervention strategy for treating TNBC by inhibiting or interfering with the interaction between NONO and PKM2.\u003c/p\u003e \u003cp\u003ePAI-1 is a major member of the serine protease inhibitor (serpin) superfamily and functions as an inhibitor of tissue-type plasminogen activator (tPA) and urokinase-type plasminogen activator (uPA) [\u003cspan citationid=\"CR51\" class=\"CitationRef\"\u003e51\u003c/span\u003e]. tPA/uPA is mainly involved in the conversion of plasminogen to active plasmin, leading to fibrin clot hydrolysis [\u003cspan citationid=\"CR51\" class=\"CitationRef\"\u003e51\u003c/span\u003e]. Therefore, PAI-1 plays an important role in various vascular disorders such as thrombosis, atherosclerosis, and myocardial infarction [\u003cspan citationid=\"CR52\" class=\"CitationRef\"\u003e52\u003c/span\u003e]. Interestingly, accumulating evidence has demonstrated that PAI-1 plays a pro-tumorigenic role in cancer, although it was originally hypothesized to have antitumor effects [\u003cspan citationid=\"CR53\" class=\"CitationRef\"\u003e53\u003c/span\u003e]. Owing to the strong correlation between PAI-1 levels and prognosis in patients with breast cancer, PAI-1 has been recommended as a biomarker for therapeutic decisions in patients with clinically node-negative breast cancer [\u003cspan citationid=\"CR54\" class=\"CitationRef\"\u003e54\u003c/span\u003e]. Several studies have shown that PAI-1 is critical for TNBC cell growth and metastasis [\u003cspan citationid=\"CR32\" class=\"CitationRef\"\u003e32\u003c/span\u003e, \u003cspan citationid=\"CR55\" class=\"CitationRef\"\u003e55\u003c/span\u003e, \u003cspan citationid=\"CR56\" class=\"CitationRef\"\u003e56\u003c/span\u003e]. In the present study, we demonstrated that NONO can recruit nuclear PKM2, which triggers the phosphorylation of histone H3 at T11 to directly activate \u003cem\u003eSERPINE1\u003c/em\u003e expression and mediate cell proliferation, migration, and invasion in TNBC cells. More importantly, NONO and PKM2 expression strongly correlated with the expression of PAI-1 in TNBC tissues. These findings identified a novel transcriptional regulatory pathway for \u003cem\u003eSERPINE1\u003c/em\u003e expression and support the function of the NONO-PKM2 interaction in the malignant progression of TNBC.\u003c/p\u003e"},{"header":"Conclusion","content":"\u003cp\u003eTaken together, our findings demonstrate that NONO interacts with nuclear PKM2 and directs histone H3 phosphorylation to promote tumor metastasis, highlighting the potential of disrupting the association between NONO and PKM2 for the targeted therapy of malignant TNBC.\u003c/p\u003e"},{"header":"Abbreviations","content":"\u003cdiv class=\"DefinitionList\"\u003e \u003cdiv class=\"DefinitionListEntry\"\u003e \u003cdiv class=\"Term\"\u003eNONO\u003c/div\u003e \u003cdiv class=\"Description\"\u003e \u003cp\u003eNon-POU domain-containing octamer-binding protein\u003c/p\u003e \u003c/div\u003e \u003c/div\u003e \u003cdiv class=\"DefinitionListEntry\"\u003e \u003cdiv class=\"Term\"\u003ePKM2\u003c/div\u003e \u003cdiv class=\"Description\"\u003e \u003cp\u003ePyruvate kinase isozyme type M2\u003c/p\u003e \u003c/div\u003e \u003c/div\u003e \u003cdiv class=\"DefinitionListEntry\"\u003e \u003cdiv class=\"Term\"\u003eH3T11ph\u003c/div\u003e \u003cdiv class=\"Description\"\u003e \u003cp\u003ePhosphorylation of histone H3 at threonine 11\u003c/p\u003e \u003c/div\u003e \u003c/div\u003e \u003cdiv class=\"DefinitionListEntry\"\u003e \u003cdiv class=\"Term\"\u003eH3K27ac\u003c/div\u003e \u003cdiv class=\"Description\"\u003e \u003cp\u003eAcetylation of histone H3 at lysine 27\u003c/p\u003e \u003c/div\u003e \u003c/div\u003e \u003cdiv class=\"DefinitionListEntry\"\u003e \u003cdiv class=\"Term\"\u003eSERPINE1\u003c/div\u003e \u003cdiv class=\"Description\"\u003e \u003cp\u003eSerine protease inhibitor family E member 1\u003c/p\u003e \u003c/div\u003e \u003c/div\u003e \u003cdiv class=\"DefinitionListEntry\"\u003e \u003cdiv class=\"Term\"\u003ePAI-1\u003c/div\u003e \u003cdiv class=\"Description\"\u003e \u003cp\u003ePlasminogen Activator Inhibitor 1\u003c/p\u003e \u003c/div\u003e \u003c/div\u003e \u003cdiv class=\"DefinitionListEntry\"\u003e \u003cdiv class=\"Term\"\u003eTNBC\u003c/div\u003e \u003cdiv class=\"Description\"\u003e \u003cp\u003eTriple-negative breast cancer\u003c/p\u003e \u003c/div\u003e \u003c/div\u003e \u003cdiv class=\"DefinitionListEntry\"\u003e \u003cdiv class=\"Term\"\u003eChIP\u003c/div\u003e \u003cdiv class=\"Description\"\u003e \u003cp\u003eChromatin immunoprecipitation\u003c/p\u003e \u003c/div\u003e \u003c/div\u003e \u003cdiv class=\"DefinitionListEntry\"\u003e \u003cdiv class=\"Term\"\u003eCUT\u0026amp;Tag\u003c/div\u003e \u003cdiv class=\"Description\"\u003e \u003cp\u003eCleavage under targets and tagmentation\u003c/p\u003e \u003c/div\u003e \u003c/div\u003e \u003cdiv class=\"DefinitionListEntry\"\u003e \u003cdiv class=\"Term\"\u003eTSS\u003c/div\u003e \u003cdiv class=\"Description\"\u003e \u003cp\u003etranscription start sites\u003c/p\u003e \u003c/div\u003e \u003c/div\u003e \u003cdiv class=\"DefinitionListEntry\"\u003e \u003cdiv class=\"Term\"\u003eIHC\u003c/div\u003e \u003cdiv class=\"Description\"\u003e \u003cp\u003eimmunohistochemical staining. DEG:Differentially expressed genes. TIP60:HIV-tat interacting protein 60kD.\u003c/p\u003e \u003c/div\u003e \u003c/div\u003e \u003c/div\u003e"},{"header":"Declarations","content":"\u003cp\u003e\u003cstrong\u003eAcknowledgments\u003c/strong\u003e\u003c/p\u003e\n\u003cp\u003eWe thank the members of the Zhao Laboratory for their helpful discussions.\u0026nbsp;\u003c/p\u003e\n\u003cp\u003e\u003cstrong\u003eAuthors\u0026rsquo; contributions\u003c/strong\u003e\u003c/p\u003e\n\u003cp\u003eQ.L., H.C., P.Z., D.Y., Y.Z., P.C., D.W., W.S., W.L., X.M., M.X., and Y.C. performed biochemical experiments and bioinformatics analysis. Q.L., H.C., P.Z., Y.C., B.C., and Z.J. performed animal experiments and provided pathology expertise. M.Z., L.K., K.Z., and D.C.S.H. provided critical reagents and expertise. Q.L., Z.J. and Q.Z. designed the project and wrote the manuscript.\u003c/p\u003e\n\u003cp\u003e\u003cstrong\u003eFunding\u003c/strong\u003e\u003c/p\u003e\n\u003cp\u003eThis work was supported by the\u0026nbsp;National Natural Science Foundation of China (NSFC #32270619 and\u0026nbsp;#31970615), Fundamental Research Fund of the\u0026nbsp;State Key Laboratory of Pharmaceutical Biotechnology\u0026nbsp;(#LNSN-202403), Key Project of Natural Science Research for\u0026nbsp;the University of Anhui Province\u0026nbsp;(No. 2023AH051989), and Natural Science Foundation of Bengbu Medical College (2021byzd141, 2023bypy013).\u003c/p\u003e\n\u003cp\u003e\u003cstrong\u003eAvailability of data and materials\u003c/strong\u003e\u003c/p\u003e\n\u003cp\u003eAll relevant data are available within the article and additional files or from the authors upon request.\u0026nbsp;Raw mass\u0026nbsp;spectrometry proteomics data\u0026nbsp;were\u0026nbsp;deposited in\u0026nbsp;the\u0026nbsp;ProteomeXchange consortium\u0026nbsp;under\u0026nbsp;the accession number PXD051842. The\u0026nbsp;RNA-Seq and CUT\u0026amp;Tag data generated for this study were deposited\u0026nbsp;in\u0026nbsp;the Gene Expression Omnibus (GSE266177, GSE266179).\u003c/p\u003e\n\u003cp\u003e\u003cstrong\u003eEthics approval and consent to participate\u003c/strong\u003e\u003c/p\u003e\n\u003cp\u003eAll experiments involving animals were conducted according to the ethical policies and procedures approved by the Animal Ethical and Welfare Committee of Nanjing University (Nanjing, China) under protocol IACUC-2112006.\u0026nbsp;\u003c/p\u003e\n\u003cp\u003e\u003cstrong\u003eConsent for publication\u003c/strong\u003e\u003c/p\u003e\n\u003cp\u003eNot applicable\u003c/p\u003e\n\u003cp\u003e\u003cstrong\u003eCompeting interests\u003c/strong\u003e\u003c/p\u003e\n\u003cp\u003eThe authors declare that they have no competing interests.\u003c/p\u003e"},{"header":"References","content":"\u003col\u003e\n\u003cli\u003eBray F, Laversanne M, Sung HYA, Ferlay J, Siegel RL, Soerjomataram I, Jemal A. 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Epithelial-mesenchymal transition induced PAI-1 is associated with prognosis of triple-negative breast cancer patients. Gene.\u003cem\u003e \u003c/em\u003e2018; 670\u003cstrong\u003e:\u003c/strong\u003e7-14.\u003c/li\u003e\n\u003c/ol\u003e"}],"fulltextSource":"","fullText":"","funders":[],"hasAdminPriorityOnWorkflow":false,"hasManuscriptDocX":true,"hasOptedInToPreprint":true,"hasPassedJournalQc":"","hasAnyPriority":false,"hideJournal":true,"highlight":"","institution":"","isAcceptedByJournal":false,"isAuthorSuppliedPdf":false,"isDeskRejected":"","isHiddenFromSearch":false,"isInQc":false,"isInWorkflow":false,"isPdf":false,"isPdfUpToDate":true,"isWithdrawnOrRetracted":false,"journal":{"display":true,"email":"[email protected]","identity":"researchsquare","isNatureJournal":false,"hasQc":true,"allowDirectSubmit":true,"externalIdentity":"","sideBox":"","snPcode":"","submissionUrl":"/submission","title":"Research Square","twitterHandle":"researchsquare","acdcEnabled":true,"dfaEnabled":false,"editorialSystem":"","reportingPortfolio":"","inReviewEnabled":false,"inReviewRevisionsEnabled":true},"keywords":"Transcription, Epigenomics, H3T11ph, NONO, PKM2, Triple-negative breast cancer, Metastasis","lastPublishedDoi":"10.21203/rs.3.rs-5280141/v1","lastPublishedDoiUrl":"https://doi.org/10.21203/rs.3.rs-5280141/v1","license":{"name":"CC BY 4.0","url":"https://creativecommons.org/licenses/by/4.0/"},"manuscriptAbstract":"\u003ch2\u003eBackground\u003c/h2\u003e \u003cp\u003eEmerging evidence has revealed that PKM2 has oncogenic functions independent of its canonical pyruvate kinase activity, serving as a protein kinase that regulates gene expression. However, the mechanism by which PKM2, as a histone kinase, regulates the transcription of genes involved in triple-negative breast cancer (TNBC) metastasis remains poorly understood.\u003c/p\u003e\u003ch2\u003eMethods\u003c/h2\u003e \u003cp\u003eWe integrated cellular analysis, including cell viability, proliferation, colony formation, and migration assays; biochemical assays, including protein interaction studies and ChIP; clinical sample analysis; RNA-Seq and CUT\u0026amp;Tag data; and xenograft or mammary-specific gene knockout mouse models, to investigate the epigenetic modulation of TNBC metastasis via NONO-dependent interactions with nuclear PKM2.\u003c/p\u003e\u003ch2\u003eResults\u003c/h2\u003e \u003cp\u003eWe report that the transcription factor NONO directly interacts with nuclear PKM2 and directs PKM2-mediated phosphorylation of histone H3 at threonine 11 (H3T11ph) to promote TNBC metastasis. We show that H3T11ph cooperates with TIP60-mediated acetylation of histone H3 at lysine 27 (H3K27ac) to activate \u003cem\u003eSERPINE1\u003c/em\u003e expression and to increase the proliferative, migratory, and invasive abilities of TNBC cells in a NONO-dependent manner. Conditional mammary loss of NONO or PKM2 markedly suppressed \u003cem\u003eSERPINE1\u003c/em\u003e expression and attenuated the malignant progression of spontaneous mammary tumors in mice. Importantly, elevated expression of NONO or PKM2 in TNBC patients is positively correlated with \u003cem\u003eSERPINE1\u003c/em\u003e expression, enhanced invasiveness, and poor clinical outcomes.\u003c/p\u003e\u003ch2\u003eConclusion\u003c/h2\u003e \u003cp\u003eThese findings revealed that the NONO-dependent interaction with nuclear PKM2 is key for the epigenetic modulation of TNBC metastasis, suggesting a novel intervention strategy for treating TNBC.\u003c/p\u003e","manuscriptTitle":"NONO directs PKM2-mediated H3T11ph to promote triple-negative breast cancer metastasis by activating SERPINE1 expression","msid":"","msnumber":"","nonDraftVersions":[{"code":1,"date":"2024-10-29 12:59:55","doi":"10.21203/rs.3.rs-5280141/v1","editorialEvents":[{"type":"communityComments","content":0}],"status":"published","journal":{"display":true,"email":"[email protected]","identity":"researchsquare","isNatureJournal":false,"hasQc":true,"allowDirectSubmit":true,"externalIdentity":"","sideBox":"","snPcode":"","submissionUrl":"/submission","title":"Research Square","twitterHandle":"researchsquare","acdcEnabled":true,"dfaEnabled":false,"editorialSystem":"","reportingPortfolio":"","inReviewEnabled":false,"inReviewRevisionsEnabled":true}}],"origin":"","ownerIdentity":"1fa35257-d0fa-47e2-93f4-97c0891ed728","owner":[],"postedDate":"October 29th, 2024","published":true,"recentEditorialEvents":[],"rejectedJournal":[],"revision":"","amendment":"","status":"posted","subjectAreas":[],"tags":[],"updatedAt":"2024-11-13T02:38:53+00:00","versionOfRecord":[],"versionCreatedAt":"2024-10-29 12:59:55","video":"","vorDoi":"","vorDoiUrl":"","workflowStages":[]},"version":"v1","identity":"rs-5280141","journalConfig":"researchsquare"},"__N_SSP":true},"page":"/article/[identity]/[[...version]]","query":{"redirect":"/article/rs-5280141","identity":"rs-5280141","version":["v1"]},"buildId":"qtupq5eGEP_6zYnWcrvyt","isFallback":false,"isExperimentalCompile":false,"dynamicIds":[84888],"gssp":true,"scriptLoader":[]}