The casein kinase 2α promotes the occurrence polycystic ovary syndrome.

Polycystic ovary syndrome (PCOS) is a complicated reproductive endocrine disease characterized by hyperandrogenism, polycystic ovaries, and anovulation. Previous studies have revealed that androgen receptors (ARs) are strongly associated with hyperandrogenism and abnormalities in folliculogenesis in patients with PCOS. However, the kinases responsible for androgen receptor activity, especially in granulosa cells, and the role of casein kinase 2α (CK2α) specifically in the pathogenesis of PCOS, remain unknown. Here, we show that both CK2α protein and mRNA levels were higher in luteinized granulosa cells of patients with PCOS compared with non-PCOS, as well as in the ovarian tissues of mice with a dehydroepiandrosterone-induced PCOS-like phenotype, compared with controls. In addition, CK2α not only interacted with AR in vivo and in vitro, but it also phosphorylated and stabilized AR, triggering AR and ovulation related genes excessive expression. CK2α also promoted cell proliferation in the KGN cell line and inhibited apoptosis. Collectively, the finding highlighted that the CK2α-AR axis probably caused the etiology of the PCOS. Thus, CK2α might be a promising clinical therapeutic target for PCOS treatment. Copyright © 2020. Published by Elsevier Inc.

Citation

Chuan-Jin Yu, Xia Liu, Zhi-Yang Zhou, Xiao-Jun Chen, Yi-Cong Meng, Hang-Chao Gu, Jing-Jing Xu, Guo-Lian Ding, Xin-Mei Liu, Jian-Zhong Sheng, He-Feng Huang. The casein kinase 2α promotes the occurrence polycystic ovary syndrome. Biochemical and biophysical research communications. 2020 Feb 17

PMID: 32081430

search → result