Tanshinone IIA inhibits the proliferation, migration and invasion of ectopic endometrial stromal cells of adenomyosis via 14-3-3ζ downregulation

article OA: closed CC0 ⤵ 14 in-corpus citations
AI-generated summary by claude@2026-06+body, 2026-06-28

Tanshinone IIA inhibited ectopic endometrial stromal cell viability, migration, and invasion while inducing apoptosis, effects mediated by 14-3-3ζ downregulation for viability, migration, and invasion.

One-sentence paraphrase of the abstract; not a substitute for reading it. No clinical advice. How this works

AI-generated deep summary by claude@2026-07, 2026-07-16 · read from full text

The study evaluated whether Tanshinone IIA (TSIIA) affects adenomyosis-associated ectopic endometrial stromal cells (EESCs) and whether its effects involve the protein 14-3-3ζ. EESCs isolated from 3 patients were treated with TSIIA, with or without adenoviral 14-3-3ζ overexpression, and outcomes were assessed using western blotting for 14-3-3ζ, CCK-8 for viability, transwell assays for migration and invasion, and flow cytometry for apoptosis. TSIIA reduced cell viability, induced apoptosis, and inhibited migration and invasion; TSIIA also decreased 14-3-3ζ expression, and 14-3-3ζ overexpression restored viability, migration, and invasion but did not reverse apoptosis, which the authors report as 14-3-3ζ-independent. The main caveat is the small sample size (3 patients) and the in vitro focus on isolated cells. This paper is centrally about endometriosis and adenomyosis — it specifically investigates TSIIA effects on ectopic endometrial stromal cells of adenomyosis via 14-3-3ζ downregulation.

Read from the paper's body, not the abstract. Not a substitute for reading the paper. No clinical advice. How this works

Abstract

BackgroundAdenomyosis is a specific subtype of endometriosis and recent evidences have indicated that Tanshinone IIA (TSIIA) might be a potential therapeutic option for endometriosis. Meanwhile, endometrial stromal cells (ESCs) of adenomyosis might play crucial roles in the progression of this disease, emphasizing the importance of targeting ESCs in the treatment of adenomyosis. Furthermore, previous evidences also implicated that deregulated 14-3-3ζ expression might be associated with therapeutic effects of certain drugs.Aim of the studyThe aim of this study is to evaluate the potential involvement of 14-3-3ζ in the process of TSIIA-treated adenomyosis.Materials and methodsEctopic endometrial stromal cells (EESCs) were isolated from a total of 3 patients with adenomyosis. Cells were treated with TSIIA and infected with 14-3-3ζ-overexpressing adenovirus, the expression level of 14-3-3ζ was determined by western blotting (WB), cell viability was detected by Cell Counting Kit-8 (CCK8), cell invasion and migration was evaluated by transwell assay, and cell apoptosis was detected by flow cytometry.ResultsTSIIA could decrease cell viability, induce cell apoptosis, and inhibit cell migration and invasion in EESCs. Mechanistically, TSIIA markedly reduced the expression of 14-3-3ζ in EESCs, and overexpression of 14-3-3ζ could restore the ability of cell viability, migration and invasion, but has no effect on cell apoptosis.ConclusionsTSIIA could be a promising novel therapeutic agent for adenomyosis, via inducing cell apoptosis, inhibiting cell viability, migration and invasion in EESCs. Furthermore, the effects of cell viability, migration and invasion were mediated in 14-3-3ζ-dependent manner while that of cell apoptosis was mediated in 14-3-3ζ-independent manner.
Full text 10,609 characters · extracted from oa-doi-fallback · 5 sections · click to expand

Abstract

Background Adenomyosis is a specific subtype of endometriosis and recent evidences have indicated that Tanshinone IIA (TSIIA) might be a potential therapeutic option for endometriosis. Meanwhile, endometrial stromal cells (ESCs) of adenomyosis might play crucial roles in the progression of this disease, emphasizing the importance of targeting ESCs in the treatment of adenomyosis. Furthermore, previous evidences also implicated that deregulated 14-3-3ζ expression might be associated with therapeutic effects of certain drugs. Aim of the study The aim of this study is to evaluate the potential involvement of 14-3-3ζ in the process of TSIIA-treated adenomyosis.

Materials and methods

Ectopic endometrial stromal cells (EESCs) were isolated from a total of 3 patients with adenomyosis. Cells were treated with TSIIA and infected with 14-3-3ζ-overexpressing adenovirus, the expression level of 14-3-3ζ was determined by western blotting (WB), cell viability was detected by Cell Counting Kit-8 (CCK8), cell invasion and migration was evaluated by transwell assay, and cell apoptosis was detected by flow cytometry.

Results

TSIIA could decrease cell viability, induce cell apoptosis, and inhibit cell migration and invasion in EESCs. Mechanistically, TSIIA markedly reduced the expression of 14-3-3ζ in EESCs, and overexpression of 14-3-3ζ could restore the ability of cell viability, migration and invasion, but has no effect on cell apoptosis.

Conclusions

TSIIA could be a promising novel therapeutic agent for adenomyosis, via inducing cell apoptosis, inhibiting cell viability, migration and invasion in EESCs. Furthermore, the effects of cell viability, migration and invasion were mediated in 14-3-3ζ-dependent manner while that of cell apoptosis was mediated in 14-3-3ζ-independent manner. Similar content being viewed by others

References

Benagiano G, Habiba M, Brosens I (2012) The pathophysiology of uterine adenomyosis: an update. Fertil Steril 98(3):572–579 Maheshwari A, Gurunath S, Fatima F et al (2012) Adenomyosis and subfertility: a systematic review of prevalence, diagnosis, treatment and fertility outcomes. Hum Reprod Update 18(4):374–392 Hudelist G, Keckstein J, Wright JT (2009) The migrating adenomyoma: past views on the etiology of adenomyosis and endometriosis. Fertil Steril 92(5):1536–1543 Genc M, Genc B, Cengiz H (2015) Adenomyosis and accompanying gynecological pathologies. Arch Gynecol Obstet 291(4):877–881 Leyendecker G, Bilgicyildirim A, Inacker M et al (2015) Adenomyosis and endometriosis. Re-visiting their association and further insights into the mechanisms of auto-traumatisation. An MRI study. Arch Gynecol Obstet 291(4):917–932 Bergeron C, Amant F, Ferenczy A (2006) Pathology and physiopathology of adenomyosis. Best Pract Res Clin Obstet Gynaecol 20(4):511–521 Liu X, Nie J, Guo SW (2011) Elevated immunoreactivity to tissue factor and its association with dysmenorrhea severity and the amount of menses in adenomyosis. Hum Reprod 26(2):337–345 Parente Barbosa C, Bentes De Souza AM, Bianco B et al (2011) The effect of hormones on endometriosis development. Minerva Ginecol 63(4):375–386 Xiong X, Yang X, Liu Y et al (2013) Chinese herbal formulas for treating hypertension in traditional Chinese medicine: perspective of modern science. Hypertens Res 36(7):570–579 Zhang HW, Lin ZX, Tung YS et al (2014) Cordyceps sinensis (a traditional Chinese medicine) for treating chronic kidney disease. Cochrane Database Syst Rev 12. doi:10.1002/14651858.CD14008353 Flower A, Liu JP, Lewith G et al (2012) Chinese herbal medicine for endometriosis. Cochrane Database Syst Rev 5. doi:10.1002/14651858.CD14006568 Yi KW, Kim SH, Ihm HJ et al (2015) Increased expression of p21-activated kinase 4 in adenomyosis and its regulation of matrix metalloproteinase-2 and -9 in endometrial cells. Fertil Steril. doi:10.1016/j.fertnstert.2014.1012.1124 Xue J, Zhang H, Liu W et al (2013) Metformin inhibits growth of eutopic stromal cells from adenomyotic endometrium via AMPK activation and subsequent inhibition of AKT phosphorylation: a possible role in the treatment of adenomyosis. Reproduction 146(4):397–406 Wang Q, Wang L, Shao J et al (2014) L-22 enhances the invasiveness of endometrial stromal cells of adenomyosis in an autocrine manner. Int J Clin Exp Pathol 7(9):5762–5771 Xu S, Liu P (2013) Tanshinone II-A: new perspectives for old remedies. Expert Opin Ther Pat 23(2):149–153 Wang J, Lu W, Wang W et al (2013) Promising therapeutic effects of sodium tanshinone IIA sulfonate towards pulmonary arterial hypertension in patients. J Thorac Dis 5(2):169–172 Shang Q, Xu H, Huang L (2012) Tanshinone IIA: a Promising Natural Cardioprotective Agent. Evid Based Complement Altern Med 2012:716459 Wei B, Li WW, Ji J et al (2014) The cardioprotective effect of sodium tanshinone IIA sulfonate and the optimizing of therapeutic time window in myocardial ischemia/reperfusion injury in rats. Atherosclerosis 235(2):318–327 Munagala R, Aqil F, Jeyabalan J et al (2015) Tanshinone IIA inhibits viral oncogene expression leading to apoptosis and inhibition of cervical cancer. Cancer Lett 356(2 Pt B):536–546 Lin LL, Hsia CR, Hsu CL et al (2015) Integrating transcriptomics and proteomics to show that tanshinone IIA suppresses cell growth by blocking glucose metabolism in gastric cancer cells. BMC Genom 16(1):41 Shen W, Zhang Y, Li W et al (2013) Effects of tanshinone on hyperandrogenism and the quality of life in women with polycystic ovary syndrome: protocol of a double-blind, placebo-controlled, randomised trial. BMJ Open 3(10):e003646 Zhou ZH, Weng Q, Zhou JH et al (2012) Extracts of Salvia miltiorrhiza Bunge on the cytokines of rat endometriosis models. Afr J Tradit Complement Altern Med 9(3):303–314 Zhao J, Meyerkord CL, Du Y et al (2011) 14-3-3 proteins as potential therapeutic targets. Semin Cell Dev Biol 22(7):705–712 Freeman AK, Morrison DK (2011) 14-3-3 Proteins: diverse functions in cell proliferation and cancer progression. Semin Cell Dev Biol 22(7):681–687 Matta A, Siu KW, Ralhan R (2012) 14-3-3 zeta as novel molecular target for cancer therapy. Expert Opin Ther Targets 16(5):515–523 Zannis-Hadjopoulos M, Yahyaoui W, Callejo M (2008) 14-3-3 cruciform-binding proteins as regulators of eukaryotic DNA replication. Trends Biochem Sci 33(1):44–50 Chen M, Liu T, Xu L et al (2014) Direct interaction of 14-3-3zeta with ezrin promotes cell migration by regulating the formation of membrane ruffle. J Mol Biol 426(18):3118–3133 Li Y, Zou L, Li Q et al (2010) Amplification of LAPTM4B and YWHAZ contributes to chemotherapy resistance and recurrence of breast cancer. Nat Med 16(2):214–218 Bergamaschi A, Christensen BL, Katzenellenbogen BS (2011) Reversal of endocrine resistance in breast cancer: interrelationships among 14-3-3zeta, FOXM1, and a gene signature associated with mitosis. Breast Cancer Res 13(3):R70 Schwab KE, Hutchinson P, Gargett CE (2008) Identification of surface markers for prospective isolation of human endometrial stromal colony-forming cells. Hum Reprod 23(4):934–943 Chan RW, Schwab KE, Gargett CE (2004) Clonogenicity of human endometrial epithelial and stromal cells. Biol Reprod 70(6):1738–1750 Tseng PY, Lu WC, Hsieh MJ et al (2014) Tanshinone IIA induces apoptosis in human oral cancer KB cells through a mitochondria-dependent pathway. Biomed Res Int 2014:540516 Wang JF, Feng JG, Han J et al (2014) The molecular mechanisms of Tanshinone IIA on the apoptosis and arrest of human esophageal carcinoma cells. Biomed Res Int 2014:582730 Chiu SC, Huang SY, Chang SF et al (2015) Potential therapeutic roles of tanshinone IIA in human bladder cancer cells. Int J Mol Sci 15(9):15622–15637 Lu Q, Zhang P, Zhang X et al (2009) Experimental study of the anti-cancer mechanism of tanshinone IIA against human breast cancer. Int J Mol Med 24(6):773–780 Lin C, Wang L, Wang H et al (2013) Tanshinone IIA inhibits breast cancer stem cells growth in vitro and in vivo through attenuation of IL-6/STAT3/NF-kB signaling pathways. J Cell Biochem 114(9):2061–2070 Gong Y, Li Y, Abdolmaleky HM et al (2012) Tanshinones inhibit the growth of breast cancer cells through epigenetic modification of Aurora A expression and function. PLoS ONE 7(4):e33656 Pan Y, Zhong LJ, Zhou H et al (2012) Roles of vimentin and 14-3-3 zeta/delta in the inhibitory effects of heparin on PC-3M cell proliferation and B16-F10-luc-G5 cells metastasis. Acta Pharmacol Sin 33(6):798–808 Zhao L, Zhou S, Zou L et al (2013) The expression and functionality of stromal caveolin 1 in human adenomyosis. Hum Reprod 28(5):1324–1338 Weimar CH, Macklon NS, Post Uiterweer ED et al (2013) The motile and invasive capacity of human endometrial stromal cells: implications for normal and impaired reproductive function. Hum Reprod Update 19(5):542–557 Shan YF, Shen X, Xie YK et al (2009) Inhibitory effects of tanshinone II-A on invasion and metastasis of human colon carcinoma cells. Acta Pharmacol Sin 30(11):1537–1542 Yamazaki S, Miyoshi N, Kawabata K et al (2014) Quercetin-3-O-glucuronide inhibits noradrenaline-promoted invasion of MDA-MB-231 human breast cancer cells by blocking beta(2)-adrenergic signaling. Arch Biochem Biophys 557:18–27 Tsai MY, Yang RC, Wu HT et al (2011) Anti-angiogenic effect of Tanshinone IIA involves inhibition of matrix invasion and modification of MMP-2/TIMP-2 secretion in vascular endothelial cells. Cancer Lett 310(2):198–206 He Y, Wu X, Liu X et al (2010) LC-MS/MS analysis of ovarian cancer metastasis-related proteins using a nude mouse model: 14-3-3 zeta as a candidate biomarker. J Proteome Res 9(12):6180–6190 Wei X, Zhou L, Hu L et al (2012) Tanshinone IIA arrests cell cycle and induces apoptosis in 786-O human renal cell carcinoma cells. Oncol Lett 3(5):1144–1148 Liu C, Li J, Wang L et al (2012) Analysis of tanshinone IIA induced cellular apoptosis in leukemia cells by genome-wide expression profiling. BMC Complement Altern Med 12:5 Acknowledgments This work was supported by the Natural Science Foundations of China (Nos. 81260097 and 81160079). Conflict of interest The authors declare that there is no conflict of interest. Author information Authors and Affiliations Corresponding author Rights and permissions About this article Cite this article Wan, L., Zou, Y., Wan, LH. et al. Tanshinone IIA inhibits the proliferation, migration and invasion of ectopic endometrial stromal cells of adenomyosis via 14-3-3ζ downregulation. Arch Gynecol Obstet 292, 1301–1309 (2015). https://doi.org/10.1007/s00404-015-3766-2 Received: Accepted: Published: Issue date: DOI: https://doi.org/10.1007/s00404-015-3766-2

Text is read by the "Ask this paper" AI Q&A widget below. Extraction quality varies by source — PMC NXML preserves structure cleanly, OA-HTML may include some navigation residue, and OA-PDF can have broken hyphenation. The publisher copy (via DOI) is the canonical version.

My notes (saved in your browser only)

Ask this paper AI returns verbatim quotes from the full text · source: oa-doi-fallback

Answers must be backed by verbatim quotes from this paper's full text. Hallucinated quotes are dropped automatically; if no verbatim passage answers the question, we say so. How this works

Condition tags

endometriosisadenomyosis

MeSH descriptors

14-3-3 Proteins Abietanes Adenomyosis Antineoplastic Agents, Phytogenic Apoptosis Cell Movement Endometrium Stromal Cells 14-3-3 Proteins 14-3-3 Proteins Abietanes Adenomyosis Adenomyosis Antineoplastic Agents, Phytogenic Apoptosis Cell Movement Cell Proliferation Cell Proliferation Cell Survival Cell Survival

Citation neighborhood

Papers in the corpus that this work cites (lower rings, blue) and that cite this one (upper rings, green). Dot size scales with the paper's in-corpus citation count — bigger dot = more influential within the endo/adeno field. Click a dot to open that paper. [ expand to 2 hops ] — adds papers reached through this work's immediate citers/citees. Heavier; up to 60 extra dots.

References (47)

Cited by (14)

Source provenance

europepmc
last seen: 2026-07-27T06:15:28.040536+00:00
openalex
last seen: 2026-06-10T17:14:06.276822+00:00
pubmed
last seen: 2026-05-13T22:17:52.213533+00:00
unpaywall
last seen: 2026-07-27T06:55:32.580041+00:00
License: CC0 · commercial use OK