Stem cell theory for the pathogenesis of endometriosis

review OA: bronze public-domain-us ⤵ 1 in-corpus citation
AI-generated summary by claude@2026-06, 2026-06-08

This paper proposes that endometriotic lesions may originate from ectopic endometrial stem/progenitor cells, adding to existing theories about retrograde menstruation and other proposed mechanisms.

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, 2026-06-10 · read from full text

This paper reviews existing hypothetical causes of endometriosis—including retrograde menstruation, lymphatic/vascular spread, iatrogenic implantation, coelomic metaplasia, embryonic rests, and mesenchymal differentiation—and argues that no single theory explains all lesion types, implying combined and/or type-specific mechanisms. It synthesizes recent evidence for endometrial stem/progenitor cells and their potential role in regenerating and differentiating eutopic endometrium. The central proposed addition is that endometriotic lesions may originate from ectopic endometrial stem/progenitor cells. The paper is a narrative review based on the current evidence rather than presenting new experimental data. This paper is centrally about endometriosis — it proposes an additional stem/progenitor-cell–based mechanism for lesion origin within endometriosis pathogenesis.

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

Abstract

Proposed hypothetical causes of endometriosis include retrograde menstruation, lymphatic and vascular metastasis, iatrogenic direct implantation, coelomic metaplasia, embryonic rest, and mesenchymal cell differentiation (induction). Each theory, individually, fails to account for all types of endometriotic lesions, thereby implicating combined and/or type-specific mechanisms. Recent evidence supports the presence of endometrial stem/progenitor cells and their possible involvement in eutopic endometrial regeneration and differentiation. Thus an additional novel mechanism for the origin of endometriotic lesions is that they arise from ectopic endometrial stem/progenitor cells.
Full text 1,412 characters · extracted from oa-doi-fallback · 2 sections · click to expand

Abstract

Proposed hypothetical causes of endometriosis include retrograde menstruation, lymphatic and vascular metastasis, iatrogenic direct implantation, coelomic metaplasia, embryonic rest, and mesenchymal cell differentiation (induction). Each theory, individually, fails to account for all types of endometriotic lesions, thereby implicating combined and/or type-specific mechanisms. Recent evidence supports the presence of endometrial stem/progenitor cells and their possible involvement in eutopic endometrial regeneration and differentiation. Thus an additional novel mechanism for the origin of endometriotic lesions is that they arise from ectopic endometrial stem/progenitor cells.

Keywords

- Endometriosis - Endometrium - Stem - Progenitor Cells - Pathogenesis - Implantation - Metaplasia - Bone Marrow - Regeneration - Endothelial Progenitor Cells - Endothelial Cells - Review

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

endometriosis

MeSH descriptors

Endometriosis Models, Theoretical Stem Cells Endometriosis Endometriosis Female Humans Stem Cells

Citation neighborhood (sparse)

Too few in-corpus citations on either side for a chart; here are the lists.

Cited by (1)

Cited by (1)

Source provenance

europepmc
last seen: 2026-06-13T06:22:48.782012+00:00
pubmed
last seen: 2026-05-13T22:16:11.197438+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