Gao Lingling, Yang Qingxing, Xu Jianbo, Wang Weijie, Lu Dan
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引用次数: 0
摘要
MiR-145-5p与多种疾病的发生和发展有关,它主要被认为是多种类型癌症的肿瘤抑制因子。据报道,在多囊卵巢综合征(PCOS)患者的颗粒细胞中,它的表达量有所下降。本研究旨在探讨 miR-145-5p 是否在颗粒细胞增殖中发挥作用,并揭示多囊卵巢综合征患者卵泡发育的潜在病理机制。研究人员采集了多囊卵巢综合征患者和健康人的卵泡液样本。采用细胞计数试剂盒-8和溴脱氧尿苷检测法评估KGN细胞的增殖情况。与对照细胞相比,多囊卵巢综合征颗粒细胞中 miR-145-5p 的表达明显减少,而 SET 的表达则有所增加。此外,miR-145-5p 还抑制了 KGN 细胞的增殖。SET被确定为miR-145-5p的直接靶标。此外,SET能促进KGN细胞的增殖,而敲除SET能抵消miR-145-5p抑制剂的作用。因此,miR-145-5p通过靶向KGN细胞中的SET来调节颗粒细胞的增殖;这一过程可能是导致多囊卵巢综合症患者卵泡发育障碍的潜在病理途径。
MiR-145-5p regulates granulosa cell proliferation by targeting the SET gene in KGN cells.
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.
期刊介绍:
Journal of Reproduction and Development (JRD) is the
official journal of the Society for Reproduction and Development,
published bimonthly, and welcomes original articles. JRD
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is based on scientific content and presentation of the materials.
The Editors select reviewers and correspond with authors. Final
decisions about acceptance or rejection of manuscripts are made
by the Editor-in-Chief and Co-Editor-in-Chief.