Department of Obstetrics and Gynecology, Faculty of Medicine, The University of Tokyo, Tokyo, Japan.
Mol Hum Reprod. 2024 Apr 30;30(5). doi: 10.1093/molehr/gaae015.
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 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, 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.
多囊卵巢综合征(PCOS)是育龄妇女中最常见的内分泌疾病之一,但它的病理尚未完全阐明,最佳治疗策略仍不清楚。细胞衰老是一种细胞周期停滞的永久状态,可以由多种应激诱导。衰老细胞由于其分泌特征的改变,即所谓的“衰老相关分泌表型”(SASP),包括促炎细胞因子的改变,而导致各种疾病的发病机制。细胞衰老选择性消除衰老细胞的一类药物,即 senolytics,目前正在临床上使用,达沙替尼和槲皮素(DQ)的组合已被广泛用作 senolytic。我们旨在研究细胞衰老是否参与 PCOS 的发病机制,以及 DQ 治疗是否对 PCOS 患者有益。我们从患有或不患有 PCOS 的患者中获得卵巢,并通过注射脱氢表雄酮建立 PCOS 小鼠模型。与对照组相比,PCOS 患者和 PCOS 小鼠的卵巢中衰老标志物 p16INK4a、p21、p53、γH2AX 和衰老相关的β-半乳糖苷酶以及 SASP 相关因子白细胞介素-6 的表达明显升高。为了评估高雄激素血症和 DQ 对体外细胞衰老的影响,我们用睾酮刺激培养的人颗粒细胞(GCs),并用 DQ 处理它们。睾酮增加了衰老标志物和 SASP 相关因子的表达,而 DQ 降低了这种增加。DQ 降低了 PCOS 小鼠卵巢中衰老标志物和 SASP 相关因子的表达,改善了其形态。这些结果表明细胞衰老发生在 PCOS 中。高雄激素血症导致 PCOS 中 GC 发生细胞衰老,而 senolytic 治疗可减少衰老 GC 的积累,并在高雄激素血症下改善卵巢形态。因此,DQ 可能代表一种治疗 PCOS 的新方法。