Fibrinogen alpha chain is up-regulated and affects the pathogenesis of endometriosis. Issue 6 (December 2019)

• Record Type: Journal Article
• Authors: Chen, Ying; Li, Hui; Cheng, Hong-yan; Rui-qiong, Ma; Ye, Xue; Cui, Heng; Hong-lan, Zhu; Chang, Xiao-hong
• Is Part Of: Reproductive biomedicine online. Volume 39:Issue 6(2019)
• Page Start: 893
• Page End: 904
• Publication Date: 2019-12
• Subjects: Endometriosis -- Fibrinogen alpha chain -- Invasion -- Migration; Human reproductive technology -- Periodicals; Human embryo -- Periodicals; Reproduction -- Periodicals; 616.692
• DOI: 10.1016/j.rbmo.2019.07.002
• Languages: English
• ISSNs: 1472-6483

Abstract

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.