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EGF-driven EGFR/miR-27b-3p/FOXO1 promotes rat FSH synthesis and secretion.

Yi-Ran MaWei GaoHao-Qi WangPei-Sen ZhaoYu-Xin ZhangFan-Hao WeiHao JiangJia-Bao ZhangBao YuanFei Gao
Published in: FASEB journal : official publication of the Federation of American Societies for Experimental Biology (2024)
The adenopituitary secretes follicle-stimulating hormone (FSH), which plays a crucial role in regulating the growth, development, and reproductive functions of organisms. Investigating the process of FSH synthesis and secretion can offer valuable insights into potential areas of focus for reproductive research. Epidermal growth factor (EGF) is a significant paracrine/autocrine factor within the body, and studies have demonstrated its ability to stimulate FSH secretion in animals. However, the precise mechanisms that regulate this action are still poorly understood. In this research, in vivo and in vitro experiments showed that the activation of epidermal growth factor receptor (EGFR) by EGF induces the upregulation of miR-27b-3p and that miR-27b-3p targets and inhibits Foxo1 mRNA expression, resulting in increased FSH synthesis and secretion. In summary, this study elucidates the precise molecular mechanism through which EGF governs the synthesis and secretion of FSH via the EGFR/miR-27b-3p/FOXO1 pathway.
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