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hsa_circRNA_BECN1 acts as a ceRNA to promote polycystic ovary syndrome progression by sponging the miR-619-5p/Rab5b axis.
- Source :
-
Molecular human reproduction [Mol Hum Reprod] 2023 Nov 01; Vol. 29 (11). - Publication Year :
- 2023
-
Abstract
- Polycystic ovary syndrome (PCOS) is a common reproductive endocrine disease that affects women of reproductive age. It is also a significant cause of infertility. Circular RNAs have been found to have a crucial role in the development and progression of reproductive system diseases. In this study, we focused on circ&#95;BECN1 and aimed to investigate its role and mechanism in PCOS, providing a foundation for early diagnosis and treatment of this condition. Our findings revealed an upregulation of circ&#95;BECN1 expression in the ovarian granulosa cells (GCs) of PCOS patients. Additionally, the silencing of circ&#95;BECN1 resulted in inhibited proliferation and enhanced apoptosis of the human ovarian granulosa-like tumor cell line (KGN), therefore implicating circ&#95;BECN1 in the cell cycle process. Through a dual-luciferase reporting assay, we determined that circ&#95;BECN1 acts as a sponge for miR-619-5p and that Rab5b is the target gene of miR-619-5p. Moreover, the expression of Rab5b was found to be upregulated in the ovarian tissue of PCOS patients. Knocking down circ&#95;BECN1 resulted in decreased Rab5b expression, which was then restored by using a miR-619-5p inhibitor. Additionally, rescue experiments demonstrated that overexpressing Rab5b reversed the effects of circ&#95;BECN1 knockdown on cell proliferation and apoptosis in KGN cells. In summary, our findings indicate that circ&#95;BECN1 is upregulated in PCOS GCs and promotes cell growth and cell cycle progression, and reduces cell apoptosis by modulating the miR-619-5p/Rab5b axis. Therefore, circ&#95;BECN1 may serve as a potential therapeutic target for PCOS treatment.<br /> (© The Author(s) 2023. Published by Oxford University Press on behalf of European Society of Human Reproduction and Embryology. All rights reserved. For permissions, please email: journals.permissions@oup.com.)
Details
- Language :
- English
- ISSN :
- 1460-2407
- Volume :
- 29
- Issue :
- 11
- Database :
- MEDLINE
- Journal :
- Molecular human reproduction
- Publication Type :
- Academic Journal
- Accession number :
- 37882757
- Full Text :
- https://doi.org/10.1093/molehr/gaad036