Overexpression of hsa-miR-132-5p in ovarian endometriotic stromal cells promoted acquisition of endometriotic phenotype

Objective: The microRNA hsa-miR-132-5p is upregulated in endometriotic cyst stromal cells (ECSCs). We investigate how hsa-miR-132-5p affects the progression of endometriosis. Methods: Normal endometrial stromal cells (NESCs) that have been isolated from normal eutopic endometrium without endometriosis and ECSCs isolated ovarian endometriotic cysts were assayed. We then evaluated how hsa-miR-132-5p impacted apoptosis, motility, and cell viability in hsa-miR-132-5p-transfected NESCs. Results: Transfection with hsa-miR-132-5p promoted cell motility and viability and inhibited the apoptosis of NESCs. Conclusions: Our results indicate that the expression of hsa-miR-132-5p promotes the acquisition of endometriosis-specific features during the progression of endometriosis. Thus, hsa-miR-132-5p may have potential value in the treatment of endometriosis.

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Publication Details

Journal
Journal of Endometriosis and Pelvic Pain Disorders
Published
2025-05-15
DOI
https://doi.org/10.1177/22840265251340361
Primary Topic
Endometriosis Research and Treatment
Type
article
Field-Weighted Citation Impact
0.00

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article

Overexpression of hsa-miR-132-5p in ovarian endometriotic stromal cells promoted acquisition of endometriotic phenotype

Kentaro Kai, Kaei Nasu, Saki Aso, Eiji Kobayashi et al.
Journal of Endometriosis and Pelvic Pain Disorders
Endometriosis Research and Treatment
article

Overexpression of hsa-miR-132-5p in ovarian endometriotic stromal cells promoted acquisition of endometriotic phenotype

Kentaro Kai, Kaei Nasu, Saki Aso, Eiji Kobayashi, Mamiko Okamoto, Yoko Aoyagi
article en

Abstract

Objective: The microRNA hsa-miR-132-5p is upregulated in endometriotic cyst stromal cells (ECSCs). We investigate how hsa-miR-132-5p affects the progression of endometriosis. Methods: Normal endometrial stromal cells (NESCs) that have been isolated from normal eutopic endometrium without endometriosis and ECSCs isolated ovarian endometriotic cysts were assayed. We then evaluated how hsa-miR-132-5p impacted apoptosis, motility, and cell viability in hsa-miR-132-5p-transfected NESCs. Results: Transfection with hsa-miR-132-5p promoted cell motility and viability and inhibited the apoptosis of NESCs. Conclusions: Our results indicate that the expression of hsa-miR-132-5p promotes the acquisition of endometriosis-specific features during the progression of endometriosis. Thus, hsa-miR-132-5p may have potential value in the treatment of endometriosis.

Journal of Endometriosis and Pelvic Pain DisordersVol. 17(4)
Oita University (JP)
Japan Society for the Promotion of Science
Openalex Percentile: Top 85%
Endometriosis Research and Treatment
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