Fibrinogen alpha chain is up-regulated and affects the pathogenesis of endometriosis

Ying Chen, Chen Y, Hui Li, Li H, Hong-Yan Cheng, Cheng HY, Ma Rui-Qiong, Rui-Qiong M, Xue Ye, Ye X, Heng Cui, Cui H, Zhu Hong-Lan, Hong-Lan Z, Xiao-Hong Chang, Chang XH
Reproductive BioMedicine Online · 2019 · vol. 39(6) , pp. 893–904 · doi:10.1016/j.rbmo.2019.07.002 · PMID:31740226
Other OA: closed public-domain-us
View on PubMed View at publisher
⚙ AI-generated summary by gemini-2.5-flash-lite, 2026-07-16 ⓘ

Fibrinogen alpha chain (FGA) expression was up-regulated in women with endometriosis and in their tissues, where it enhanced cell adhesion, migration, and invasion, potentially contributing to the disease's pathogenesis.

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

Abstract

RESEARCH QUESTION: In the group's previous study, fibrinogen alpha chain (FGA) was identified as an up-regulated differential protein that was highly expressed in women with endometriosis. The current study investigated the expression and effects of FGA in endometriosis. It also evaluated the effects of FGA on human endometrial stromal cells and studied the possible mechanism. DESIGN: This was a cross-sectional analysis of FGA expression in plasma and endometrial tissue of matched eutopic and ectopic samples from women with endometriosis undergoing laparoscopic surgery and samples from women without endometriosis. Forty-four patients with endometriosis and 32 healthy control subjects who donated plasma for FGA analysis, including 26 matched cases of eutopic and ectopic endometria from endometriosis patients and 22 endometria from healthy control subjects, were analysed. The effects of FGA were studied in a human endometrial stromal cell line after transfection with FGA short interfering RNA (siRNA). RESULTS: FGA concentrations in serum and expression in eutopic and ectopic endometrial tissue were significantly higher in women with endometriosis than controls (P < 0.05 and P < 0.01 respectively), whereas FGA expression was not significantly different in eutopic compared with ectopic endometrial tissues from the same patients. High FGA concentrations in serum were related to disease stage and ovarian involvement, but were not affected by age and menstrual cycle. The knockdown of FGA expression by FGA siRNA inhibited hEM15A cellular adhesion, migration and invasion, and attenuated matrix metalloproteinase-2 (MMP-2) expression. CONCLUSIONS: High FGA expression in endometriosis was closely related to disease severity and affected cell adhesion, migration and invasion, which might play an important role in the pathogenesis of endometriosis.

My notes (saved in your browser only)

Condition tags

endometriosis

MeSH descriptors

Endometriosis Endometrium Fibrinogen Adult Adult Apoptosis Apoptosis Case-Control Studies Case-Control Studies Cell Adhesion Cell Adhesion Cell Line Cell Line Cell Movement Cell Movement Cell Proliferation Cell Proliferation Endometriosis Endometriosis Endometriosis

Funding

funders
[{'doi': '10.13039/501100001809', 'name': 'National Natural Science Foundation of China', 'awards': []}]

Citation neighborhood (2-hop)

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. Outer rings show 2-hop neighbours — papers reached through the immediate citers/citees. [ collapse to 1-hop ]

References (27)

Source provenance

crossref
last seen: 2026-08-20T06:29:56.412022+00:00
europepmc
last seen: 2026-10-16T06:09:50.462052+00:00
pubmed
last seen: 2026-10-08T21:26:00.687991+00:00
unpaywall
last seen: 2026-10-16T06:24:35.758740+00:00
License: public-domain-us · commercial use OK · attribution required
Courtesy of the U.S. National Library of Medicine