Lingling Gao, Qingxing Yang, Jianbo Xu, Weijie Wang, Dan Lu
Department of Obstetrics and Gynecology, Northern Jiangsu People's Hospital Affiliated to Yangzhou University, Jiangsu 225001, China.
Department of Obstetrics and Gynecology, Northern Jiangsu People's Hospital, Jiangsu 225001, China.
J Reprod Dev. 2024 Dec 13;70(6):372-378. doi: 10.1262/jrd.2024-053. Epub 2024 Sep 22.
MiR-145-5p has been implicated in the development and progression of various disorders, and it is primarily recognized as a tumor suppressor in numerous cancers types. Its expression has been reported to decrease in the granulosa cells of patients with polycystic ovarian syndrome (PCOS). This study aimed to investigate whether miR-145-5p plays a role in granulosa cell proliferation and to shed light on the underlying pathological mechanisms of follicular development in patients with PCOS. Follicular fluid samples were collected from patients with PCOS and healthy individuals. The Cell Counting Kit-8 and bromodeoxyuridine assays were performed to assess KGN cell proliferation. The expression of miR-145-5p was significantly decreased in PCOS granulosa cells than in control cells, whereas the expression of SET was increased. Furthermore, miR-145-5p suppressed the proliferation of KGN cells. SET was identified as a direct target of miR-145-5p. Additionally, SET promoted the proliferation of KGN cells, and knockdown of SET counteracted the effect of the miR-145-5p inhibitor. Therefore, miR-145-5p regulates granulosa cell proliferation by targeting the SET in KGN cells; this process may be a potential pathological pathway that contributes to follicular developmental disorders in PCOS.
MiR-145-5p与多种疾病的发生发展有关,在多种癌症类型中它主要被视为一种肿瘤抑制因子。据报道,多囊卵巢综合征(PCOS)患者的颗粒细胞中其表达会降低。本研究旨在探讨miR-145-5p是否在颗粒细胞增殖中发挥作用,并阐明PCOS患者卵泡发育的潜在病理机制。从PCOS患者和健康个体中收集卵泡液样本。采用细胞计数试剂盒-8和溴脱氧尿苷检测法评估KGN细胞增殖。PCOS颗粒细胞中miR-145-5p的表达明显低于对照细胞,而SET的表达则升高。此外,miR-145-5p抑制KGN细胞的增殖。SET被确定为miR-145-5p的直接靶点。此外,SET促进KGN细胞的增殖,敲低SET可抵消miR-145-5p抑制剂的作用。因此,miR-145-5p通过靶向KGN细胞中的SET来调节颗粒细胞增殖;这一过程可能是导致PCOS患者卵泡发育障碍的潜在病理途径。