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LNK promotes granulosa cell apoptosis in PCOS via negatively regulating insulin-stimulated AKT-FOXO3 pathway

Min Tan, Yanxiang Cheng, Xiaozhu Zhong, Dongyong Yang, Sushi Jiang, Yang Ye, Miao Ding, Guijun Guan, Dongzi Yang, Xiaomiao Zhao

2021Aging70 citationsDOIOpen Access PDF

Abstract

BACKGROUND: Polycystic ovary syndrome (PCOS), which is often accompanied by insulin resistance, is closely related to increased apoptosis of ovarian granulosa cells. LNK is an important regulator of the insulin signaling pathway. When insulin binds to the receptor, the PI3K/AKT/FOXO signaling pathway is activated, and FOXO translocates from the nucleus to the cytoplasm, thereby inhibiting the expression of pro-apoptotic genes. METHODS: knockout mice were used to investigate the effect of LNK on the pathogenesis of PCOS. RESULTS: knockout partially restored estrous cycle and improved glucose metabolism in PCOS mice. CONCLUSIONS: knockout partially restored estrous cycle and improved glucose metabolism in PCOS mice, suggesting LNK might become a potential biological target for the clinical treatment of PCOS.

Topics & Concepts

FOXO3Protein kinase BApoptosisInsulinCell biologyEndocrinologyInternal medicineChemistryBiologyMedicineBiochemistryFOXO transcription factor regulationReproductive Biology and Fertility
LNK promotes granulosa cell apoptosis in PCOS via negatively regulating insulin-stimulated AKT-FOXO3 pathway | Litcius