» Articles » PMID: 26681917

Regulation of Androgen Receptor Expression Alters AMPK Phosphorylation in the Endometrium: In Vivo and In Vitro Studies in Women with Polycystic Ovary Syndrome

Overview
Journal Int J Biol Sci
Specialty Biology
Date 2015 Dec 19
PMID 26681917
Citations 21
Authors
Affiliations
Soon will be listed here.
Abstract

The failure of reproductive success in polycystic ovary syndrome (PCOS) patients could be in part due to endometrial dysfunction. However, no studies have investigated any causality between androgen, androgen receptor (AR) expression, and adenosine monophosphate activated protein kinase (AMPK) activation in the endometrium under physiological and pathological conditions. In the present study, we show that 1) endometrial AR expression levels fluctuate in non-PCOS and PCOS patients during the menstrual cycle; 2) the menstrual phase-dependent alteration of p-AMPKα expression occurs in non-PCOS patients but not in PCOS patients; 3) AR expression is higher in PCOS patients than non-PCOS patients during hyperplasia while AMPKα activation (indicated by the ratio of p-AMPKα to AMPKα); and 4) co-localization of AR and Ki-67 in epithelial cell nuclei is observed in endometrial hyperplasia. Importantly, using in vitro human tissue culture and an in vivo 5α-dihydrotestosterone-treated rat model, we show that the action of androgen on AMPKα activation is likely mediated through nuclear AR, especially in epithelial cells. Collectively, we present evidence that AR expression and AMPKα activation depend on menstrual cycle phase and the presence of PCOS, and the data suggest that AR-mediated regulation of AMPKα activation might play a role in the development of endometrial hyperplasia.

Citing Articles

A Comprehensive Review of the Contribution of Mitochondrial DNA Mutations and Dysfunction in Polycystic Ovary Syndrome, Supported by Secondary Database Analysis.

Kobayashi H, Matsubara S, Yoshimoto C, Shigetomi H, Imanaka S Int J Mol Sci. 2025; 26(3).

PMID: 39940939 PMC: 11818232. DOI: 10.3390/ijms26031172.


Decreased AMPK/SIRT1/PDK4 induced by androgen excess inhibits human endometrial stromal cell decidualization in PCOS.

Hong L, Xiao S, Diao L, Lian R, Chen C, Zeng Y Cell Mol Life Sci. 2024; 81(1):324.

PMID: 39080028 PMC: 11335245. DOI: 10.1007/s00018-024-05362-5.


Androgen excess: a hallmark of polycystic ovary syndrome.

Wang K, Li Y, Chen Y Front Endocrinol (Lausanne). 2023; 14:1273542.

PMID: 38152131 PMC: 10751361. DOI: 10.3389/fendo.2023.1273542.


Role of Hormones During Gestation and Early Development: Pathways Involved in Developmental Programming.

Abruzzese G, Campo Verde Arbocco F, Ferrer M, Silva A, Motta A Adv Exp Med Biol. 2023; 1428:31-70.

PMID: 37466768 DOI: 10.1007/978-3-031-32554-0_2.


Diane-35 and metformin therapy in rats with endometrial lesions induced by dihydrotestosterone exposure.

Liu Y, Xu R, Zhou Y, Wang Y, Zhang F, Tong X Ann Transl Med. 2023; 11(6):247.

PMID: 37082665 PMC: 10113095. DOI: 10.21037/atm-21-2441.


References
1.
Shao R, Li X, Feng Y, Lin J, Billig H . Direct effects of metformin in the endometrium: a hypothetical mechanism for the treatment of women with PCOS and endometrial carcinoma. J Exp Clin Cancer Res. 2014; 33:41. PMC: 4036091. DOI: 10.1186/1756-9966-33-41. View

2.
Shirwany N, Zou M . AMPK: a cellular metabolic and redox sensor. A minireview. Front Biosci (Landmark Ed). 2014; 19(3):447-74. PMC: 4101001. DOI: 10.2741/4218. View

3.
Marshall E, Lowrey J, Macpherson S, Maybin J, Collins F, Critchley H . In silico analysis identifies a novel role for androgens in the regulation of human endometrial apoptosis. J Clin Endocrinol Metab. 2011; 96(11):E1746-55. PMC: 3380091. DOI: 10.1210/jc.2011-0272. View

4.
Long Y, Zierath J . AMP-activated protein kinase signaling in metabolic regulation. J Clin Invest. 2006; 116(7):1776-83. PMC: 1483147. DOI: 10.1172/JCI29044. View

5.
Lang F, Alevizopoulos K, Stournaras C . Targeting membrane androgen receptors in tumors. Expert Opin Ther Targets. 2013; 17(8):951-63. DOI: 10.1517/14728222.2013.806491. View