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Cellular senescence of granulosa cells in the pathogenesis of polycystic ovary syndrome

Tsurugi Tanaka, Yoko Urata, Miyuki Harada, Chisato Kunitomi, Akari Kusamoto, Hiroshi Koike, Zixin Xu, Nanoka Sakaguchi, Chihiro Tsuchida, Airi Komura, Ayaka Teshima, Nozomi Takahashi, Osamu Wada‐Hiraike, Yasushi Hirota, Yutaka Osuga

Molecular Human Reproduction · 2024 · ▲ 13 citations

Abstract

Polycystic ovary syndrome (PCOS) is one of the most common endocrine disorders in women of reproductive age, but its pathology has not been fully characterized and the optimal treatment strategy remains unclear. Cellular senescence(definition) is a permanent state of cell-cycle arrest that can be induced by multiple stresses. Senescent cells contribute to the pathogenesis of various diseases, owing to an alteration in secretory profile, termed 'senescence-associated secretory phenotype' (SASP), including with respect to pro-inflammatory cytokines. Senolytics(definition), a class of drugs that selectively eliminate senescent cells, are now being used clinically, and a combination of dasatinib and quercetin (DQ) has been extensively used as a senolytic. We aimed to investigate whether cellular senescence is involved in the pathology of PCOS and whether DQ treatment has beneficial effects in patients with PCOS. We obtained ovaries from patients with or without PCOS, and established a mouse model of PCOS by injecting dehydroepiandrosterone. The expression of the senescence markers p16INK4a, p21, p53, γH2AX, and senescence-associated β-galactosidase and the SASP-related factor interleukin-6 was significantly higher in the ovaries of patients with PCOS and PCOS mice than in controls. To evaluate the effects of hyperandrogenism and DQ on cellular senescence in vitro, we stimulated cultured human granulosa cells (GCs) with testosterone and treated them with DQ. The expression of markers of senescence and a SASP-related factor was increased by testosterone, and DQ reduced this increase. DQ reduced the expression of markers of senescence and a SASP-related factor in the ovaries of PCOS mice and improved their morphology. These results indicate that cellular senescence occurs in PCOS. Hyperandrogenism causes cellular senescence in GCs in PCOS, and senolytic treatment reduces the accumulation of senescent GCs and improves ovarian morphology under hyperandrogenism. Thus, DQ might represent a novel therapy for PCOS.

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Provenance

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OpenAlex
DOI
10.1093/molehr/gaae015
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2026-06-19 MST

Cite this

APA
Tanaka, T., Urata, Y., Harada, M., Kunitomi, C., Kusamoto, A., Koike, H., Xu, Z., Sakaguchi, N., Tsuchida, C., Komura, A., Teshima, A., Takahashi, N., Wada‐Hiraike, O., Hirota, Y., &amp; Osuga, Y. (2024). Cellular senescence of granulosa cells in the pathogenesis of polycystic ovary syndrome. <em>Molecular Human Reproduction</em>. https://doi.org/10.1093/molehr/gaae015
Vancouver
Tanaka T, Urata Y, Harada M, Kunitomi C, Kusamoto A, Koike H, et al. Cellular senescence of granulosa cells in the pathogenesis of polycystic ovary syndrome. Molecular Human Reproduction. 2024. doi:10.1093/molehr/gaae015.
BibTeX
@article{tsurugi2024Cellul, title = {Cellular senescence of granulosa cells in the pathogenesis of polycystic ovary syndrome}, author = {Tsurugi Tanaka and Yoko Urata and Miyuki Harada and Chisato Kunitomi and Akari Kusamoto and Hiroshi Koike and Zixin Xu and Nanoka Sakaguchi and Chihiro Tsuchida and Airi Komura and Ayaka Teshima and Nozomi Takahashi and Osamu Wada‐Hiraike and Yasushi Hirota and Yutaka Osuga}, journal = {Molecular Human Reproduction}, year = {2024}, doi = {10.1093/molehr/gaae015}, }

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