Association between Morphological Patterns of Myometrial Invasion and Cancer Stem Cell Markers in Endometrial Endometrioid Carcinoma

other OA: closed public-domain-us
Full text JSON View on PubMed View at publisher
AI-generated summary by claude@2026-06, 2026-06-13

This study analyzed myometrial invasion patterns in endometrial endometrioid adenocarcinoma and found infiltrating/MELF patterns are associated with high grade, reduced hormone receptors, CSC markers, and lymph node metastasis, indicating a worse prognosis.

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

AI-generated deep summary by claude@2026-06, 2026-06-13 · read from full text

This study examined 73 cases of endometrial endometrioid carcinoma with myometrial invasion to assess how different invasion morphology patterns relate to cancer stem cell (CSC) marker expression and clinicopathological outcomes. Myometrial invasion patterns on hematoxylin-and-eosin slides were categorized as infiltrating, expansile, adenomyosis (AM)-like, or MELF-type, and immunohistochemistry evaluated CSC markers CD44, CD133, and Nanog1 along with estrogen and progesterone receptor status; age, depth of invasion, lymphovascular invasion, lymph node metastasis, progression, and survival were also recorded. Tumors with infiltrating invasion were associated with higher FIGO grade, reduced ER/PR, and higher CD44 expression, while MELF-type invasion was associated with lymph node metastasis and lymphovascular invasion and with reduced ER, CD44, and CD133; the authors reported that infiltrating/MELF patterns corresponded to worse prognosis and an unfavorable CSC expression profile. Limitations included reliance on immunohistochemical marker expression within a retrospective case series rather than functional characterization of CSCs. Relevance to endometriosis and adenomyosis: although the paper is about endometrial endometrioid carcinoma and myometrial invasion morphology, it explicitly includes an “adenomyosis (AM)-like” invasion pattern category, which directly ties the invasion pattern framework to adenomyosis-like histology in the context of endometriosis-related disease research.

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

Abstract

In endometrial endometrioid adenocarcinoma (EEC), the depth of myometrial invasion (MI) is an important parameter for determining whether additional treatment is warranted. The present study investigated the association between MI patterns, cancer stem cell (CSC) phenotypes, and their clinicopathological significance in EEC. A total of 73 cases of EEC with MI were examined in this study. Haematoxylin and eosin-stained tissue specimens were analysed for MI pattern, which was categorised as infiltrating; expansile; adenomyosis (AM)-like; or microcystic, elongated, and fragmented (MELF)-type. The expression of CSC markers such as cluster of differentiation (CD)44, CD133, and Nanog1, as well as oestrogen receptor (ER) and progesterone receptor (PR) was examined by immunohistochemistry. Clinicopathological features including age, DOI, MI pattern, LVI, lymph node (LN) metastasis, disease progression, and survival outcome were recorded. Most examined cases (45/73) were International Federation of Gynecology and Obstetrics (FIGO) stage I. MI showed infiltrating (49.3%), AM-like (26.3%), MELF (15.1%), and expansile (9.6%) patterns. Tumours with the infiltrating pattern were associated with high FIGO grade (P = 0.002), reduced ER and PR, and CD44 expression (P = 0.014, 0.026, and 0.030, respectively); those with a MELF pattern showed LN metastasis (P < 0.001), lymphovascular invasion (P = 0.011), and reduced ER, CD44, and CD133 expression (P = 0.036, 0.006, and 0.016, respectively). EEC with infiltrating/MELF patterns of MI is associated with worse prognosis. These results suggest that CSC expression profiles are an unfavourable indicator of EEC.
Full text 9,759 characters · extracted from oa-doi-fallback · 2 sections · click to expand

Abstract

In endometrial endometrioid adenocarcinoma (EEC), the depth of myometrial invasion (MI) is an important parameter for determining whether additional treatment is warranted. The present study investigated the association between MI patterns, cancer stem cell (CSC) phenotypes, and their clinicopathological significance in EEC. A total of 73 cases of EEC with MI were examined in this study. Haematoxylin and eosin-stained tissue specimens were analysed for MI pattern, which was categorised as infiltrating; expansile; adenomyosis (AM)-like; or microcystic, elongated, and fragmented (MELF)-type. The expression of CSC markers such as cluster of differentiation (CD)44, CD133, and Nanog1, as well as oestrogen receptor (ER) and progesterone receptor (PR) was examined by immunohistochemistry. Clinicopathological features including age, DOI, MI pattern, LVI, lymph node (LN) metastasis, disease progression, and survival outcome were recorded. Most examined cases (45/73) were International Federation of Gynecology and Obstetrics (FIGO) stage I. MI showed infiltrating (49.3%), AM-like (26.3%), MELF (15.1%), and expansile (9.6%) patterns. Tumours with the infiltrating pattern were associated with high FIGO grade (P = 0.002), reduced ER and PR, and CD44 expression (P = 0.014, 0.026, and 0.030, respectively); those with a MELF pattern showed LN metastasis (P < 0.001), lymphovascular invasion (P = 0.011), and reduced ER, CD44, and CD133 expression (P = 0.036, 0.006, and 0.016, respectively). EEC with infiltrating/MELF patterns of MI is associated with worse prognosis. These results suggest that CSC expression profiles are an unfavourable indicator of EEC. Access this article We’re sorry, something doesn't seem to be working properly. Please try refreshing the page. If that doesn't work, please contact support so we can address the problem. Similar content being viewed by others Abbreviations - AM: - adenomyosis - CD: - cluster of differentiation - EEC: - endometrial endometrioid carcinoma - ER: - oestrogen receptor - CSC: - cancer stem cells - DOI: - depth of invasion - EMT: - epithelial-mesenchymal transition - FIGO: - International Federation of Gynecology and Obstetrics - LN: - lymph node. - LNI: - lymph node involvement. - LUS: - lower uterine segment. - LVI: - lymphovascular invasion. - MELF: - microcystic, elongated, and fragmented. - MI: - myometrial invasion. - PR: - progesterone receptor.

References

Cole AJ, Quick CM (2013) Patterns of myoinvasion in endometrial adenocarcinoma: recognition and implications. Adv Anat Pathol 20(3):141–147 Euscher E, Fox P, Bassett R, Al-Ghawi H, Ali-Fehmi R, Barbuto D, Malpica A (2013) The pattern of myometrial invasion as a predictor of lymph node metastasis or extrauterine disease in low-grade endometrial carcinoma. Am J Surg Pathol 37(11):1728–1736 Clarke MF, Dick JE, Dirks PB, Eaves CJ, Jamieson CH, Jones DL, Wahl GM (2006) Cancer stem cells–perspectives on current status and future directions: AACR Workshop on cancer stem cells. Cancer Res 66(19):9339–9344 Lapidot T, Sirard C, Vormoor J, Murdoch B, Hoang T, Caceres-Cortes J, Dick JE (1994) A cell initiating human acute myeloid leukaemia after transplantation into SCID mice. Nature 367(6464):645–648 Al-Hajj M, Wicha MS, Benito-Hernandez A, Morrison SJ, Clarke MF (2003) Prospective identification of tumorigenic breast cancer cells. Proc Natl Acad Sci U S A 100(7):3983–3988 Singh SK, Hawkins C, Clark ID, Squire JA, Bayani J, Hide T, Dirks PB (2004) Identification of human brain tumour initiating cells. Nature 432(7015):396–401 Brendel C, Scharenberg C, Dohse M, Robey RW, Bates SE, Shukla S, Neubauer A (2007) Imatinib mesylate and nilotinib (AMN107) exhibit high-affinity interaction with ABCG2 on primitive hematopoietic stem cells. Leukemia 21(6):1267–1275 Fan X, Matsui W, Khaki L, Stearns D, Chun J, Li YM, Eberhart CG (2006) Notch pathway inhibition depletes stem-like cells and blocks engraftment in embryonal brain tumors. Cancer Res 66(15):7445–7452 Phillips TM, McBride WH, Pajonk F (2006) The response of CD24(−/low)/CD44+ breast cancer-initiating cells to radiation. J Natl Cancer Inst 98(24):1777–1785 Szotek PP, Pieretti-Vanmarcke R, Masiakos PT, Dinulescu DM, Connolly D, Foster R, Donahoe PK (2006) Ovarian cancer side population defines cells with stem cell-like characteristics and Mullerian Inhibiting Substance responsiveness. Proc Natl Acad Sci U S A 103(30):11154–11159 Bissell MJ, Radisky D (2001) Putting tumours in context. Nat Rev Cancer 1(1):46–54 Gupta GP, Massague J (2006) Cancer metastasis: building a framework. Cell 127(4):679–695 Hu M, Polyak K (2008) Microenvironmental regulation of cancer development. Curr Opin Genet Dev 18(1):27–34 Mirantes C, Espinosa I, Ferrer I, Eaton EN, Ayyanan A, Zhou AY, Weinberg RA (2013) Epithelial-to-mesenchymal transition and stem cells in endometrial cancer. Hum Pathol 44(10):1973–1981 Hollier BG, Evans K, Mani SA The epithelial-to-mesenchymal transition and cancer stem cells: a coalition against cancer therapies. J Mammary Gland Biol Neoplasia 14(1):29–43 Hugo H, Ackland ML, Blick T, Lawrence MG, Clements JA, Williams ED, Thompson EW (2007) Epithelial-mesenchymal and mesenchymal-epithelial transitions in carcinoma progression. J Cell Physiol 213(2):374–383 Singh A, Settleman J (2010) EMT, cancer stem cells and drug resistance: an emerging axis of evil in the war on cancer. Oncogene 29(34):4741–4751 Mani SA, Guo W, Liao MJ, Dolcet X, Prat J, Matias-Guiu X (2008) The epithelial-mesenchymal transition generates cells with properties of stem cells. Cell 133(4):704–715 Nakamura M, Kyo S, Zhang B, Zhang X, Mizumoto Y, Takakura M, Inoue M (2010) Prognostic impact of CD133 expression as a tumor-initiating cell marker in endometrial cancer. Hum Pathol 41(11):1516–1529 Mizrak D, Brittan M, Alison M (2008) CD133: molecule of the moment. J Pathol 214(1):3–9 Hammond ME, Hayes DE, Dowsett M, Allred DC, Hagerty KL, Badve S American Society of Clinical Oncology/College of American Pathologists guideline recommendations for immunohistochemical testing of estrogen and progesterone receptors in breast cancer (unabridged version). Arch Pathol Lab Med 134(7):48–72 Koyuncuoglu M, Okysy E, Saatli B, Olgan S, Akin M, Saygili U (2012) Tumor budding and E-Cadherin expression in endometrial carcinoma: are they prognostic factors in endometrial cancer? Gynecol Oncol 125(1):208–213 Rutella S, Bonanno G, Procoli A, Mariotti A, Corallo M, Prisco MG, Ferrandina G (2009) Cells with characteristics of cancer stem/progenitor cells express the CD133 antigen in human endometrial tumors. Clin Cancer Res 15(13):4299–4311 Friel AM, Zhang L, Curley MD, Therrien VA, Sergent PA, Belden SE, Rueda BR (2010) Epigenetic regulation of CD133 and tumorigenicity of CD133 positive and negative endometrial cancer cells. Reprod Biol Endocrinol 8:147–160 Zagorianakou N, Ioachim E, Mitselou A, Kitsou E, Zagorianakou P, Stefanaki S, Agnantis NJ (2003) Glycoprotein CD44 expression in normal, hyperplasic and neoplastic endometrium. An immunohistochemical study including correlations with p53, steroid receptor status and proliferative indices (PCNA, MIB1). Eur J Gynaecol Oncol 24(6):500–504 Murray SK, Young RH, Scully RE (2003) Unusual epithelial and stromal changes in myoinvasive endometrioid adenocarcinoma: a study of their frequency, associated diagnostic problems, and prognostic significance. Int J Gynecol Pathol 22(4):324–333 Castilla MA, Moreno-Bruno G, Romero-Perez L, Van De Vijver K, Biscuola M, Lopez-Garcia MA, Palacios J (2011) Micro-RNA signature of the epithelial-mesenchymal transition in endometrial carcinosarcoma. J Pathol 223(1):72–80 Wik E, Raeder MB, Krakstad C, Trovik J, Birkeland E, Hoivik EA, Salvesen HB (2013) Lack of estrogen receptor-alpha is associated with epithelial-mesenchymal transition and PI3K alterations in endometrial carcinoma. Clin Cancer Res 19(5):1094–1105 Stewart CJ, Little L (2009) Immunophenotypic features of MELF pattern invasion in endometrial adenocarcinoma: evidence for epithelial-mesenchymal transition. Histopathology 55(1):91–101 Hanekamp EE, Gielen SC, De Ruiter PE, Chadha-Ajwani S, Brinkmann AO, Blok LJ (2005) Differences in invasive capacity of endometrial cancer cell lines expressing different progesterone receptor isotypes: possible involvement of cadherins. J Soc Gynecol Investig 12(4):278–284 Dai D, Wolf DM, Litman ES, White MJ, Leslie KK (2002) Progesterone inhibits human endometrial cancer cell growth and invasiveness: down-regulation of cellular adhesion molecules through progesterone B receptors. Cancer Res 62(3):881–886 Hanekamp EE, Kuhne EC, Smid-Koopman E, Chadha-Ajwani S, Huikeshoven FJ, Burger CW, Blok LJ (2002) Loss of progesterone receptor may lead to an invasive phenotype in human endometrial cancer. Eur J Cancer 38(Suppl 6):S71–SS2 Guarino M, Rubino B, Ballabio G (2007) The role of epithelial-mesenchymal transition in cancer pathology. Pathology 39(3):305–318 Thiery JP (2002) Epithelial-mesenchymal transitions in tumour progression. Nat Rev Cancer 2(6):442–454 Acknowledgments This work was supported by Biomedical Research Institute grant, Kyungpook National University Hospital (2014). Author information Authors and Affiliations Corresponding author Ethics declarations Conflict of Interest The authors declare that they have no conflict of interest. Rights and permissions About this article Cite this article Park, J.Y., Hong, D. & Park, J.Y. Association between Morphological Patterns of Myometrial Invasion and Cancer Stem Cell Markers in Endometrial Endometrioid Carcinoma. Pathol. Oncol. Res. 25, 123–130 (2019). https://doi.org/10.1007/s12253-017-0320-5 Received: Accepted: Published: Issue date: DOI: https://doi.org/10.1007/s12253-017-0320-5

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

adenomyosis

MeSH descriptors

Biomarkers, Tumor Carcinoma, Endometrioid Endometrial Neoplasms Epithelial-Mesenchymal Transition Myometrium Neoplastic Stem Cells Adult Aged Biomarkers, Tumor Carcinoma, Endometrioid Carcinoma, Endometrioid Carcinoma, Endometrioid Case-Control Studies Endometrial Neoplasms Endometrial Neoplasms Endometrial Neoplasms Female Follow-Up Studies Humans Lymphatic Metastasis

Citation neighborhood (no data yet)

We don't have any in-corpus citations linked to this paper yet. The paper's references may be in our DB but unresolved to ``paper_id`` (resolution happens at ingest when the cited DOI matches a row we already have). Run the cross-source citation reconcile pass to retry.

Source provenance

europepmc
last seen: 2026-06-19T06:14:56.452680+00:00
pubmed
last seen: 2026-05-13T22:20:13.663096+00:00
unpaywall
last seen: 2026-05-14T19:30:52.867331+00:00
License: public-domain-us · commercial use OK · attribution required
Courtesy of the U.S. National Library of Medicine