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Published on: September 17, 2021
NADPH oxidase 4-mediating oxidative stress contributes to endometriosis
Xiaojie Wang1, Xiaona Jiang1, Xin Lv1
1Department of Gynecology, the Affiliated Yantai Yuhuangding Hospital of Qingdao University, No.20 Yuhuangding East Road, Yantai, 264000, Shandong, China.
Abstract:
NADPH oxidase 4 (NOX4) plays an important role in the regulation of oxidative stress, which is associated with endometriosis. This study aims to investigate the effects of NOX4 in endometriosis and its molecular mechanisms. Clinical specimens were collected, and human endometrial stromal cells (HESCs) were isolated. The knockdown of NOX4 cell lines was established on the HESCs and induced by peritoneal fluid. The levels of NOX4 were determined by using immunohistochemistry (IHC) staining, western blotting, and qPCR, respectively. The levels of oxidative stress markers were determined by using western blotting and ELISAs, respectively. The correlation of NOX4 and oxidative stress markers was analyzed by the Pearson correlation coefficient. The levels of NOX4 were dramatically elevated in the ectopic endometrium. Besides, oxidative stress biomarkers were also dysregulated in the ectopic endometrium as compared to the normal endometrium. Pearson's correlation coefficient analysis revealed a relationship between NOX4 and oxidative stress biomarkers in the ectopic endometrium. NOX4 modulated the expressions of oxidative stress markers in endometrial stromal cells stimulated by the peritoneal fluid from endometriosis. The effects of NOX4 on endometriosis are in part by its regulatory effects against oxidative stress.
Insights
NADPH oxidase 4 (NOX4) is elevated in endometriosis and linked to oxidative stress. Targeting NOX4 may offer a therapeutic strategy by regulating oxidative stress markers in endometrial cells.
Area of Science:
- Reproductive Biology
- Molecular Biology
- Cell Biology
Background:
- Endometriosis is a condition linked to oxidative stress.
- NADPH oxidase 4 (NOX4) is implicated in regulating oxidative stress.
Purpose of the Study:
- To investigate the role of NOX4 in endometriosis.
- To elucidate the molecular mechanisms of NOX4 in this condition.
Main Methods:
- Collected clinical specimens and isolated human endometrial stromal cells (HESCs).
- Established NOX4 knockdown HESC lines and induced them with peritoneal fluid.
- Quantified NOX4 and oxidative stress markers using IHC, western blotting, qPCR, and ELISAs.
- Analyzed correlations using Pearson correlation coefficient.
Main Results:
- NOX4 levels were significantly higher in ectopic endometrium compared to normal endometrium.
- Oxidative stress biomarkers were dysregulated in ectopic endometrium.
- A positive correlation was found between NOX4 and oxidative stress biomarkers.
- NOX4 modulated oxidative stress markers in HESCs stimulated by endometriosis peritoneal fluid.
Conclusions:
- NOX4 is upregulated in endometriosis and associated with oxidative stress.
- NOX4 plays a role in endometriosis pathogenesis, partly through regulating oxidative stress.
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