期刊名称：Proceedings of the National Academy of Sciences
印刷版ISSN：0027-8424
电子版ISSN：1091-6490
出版年度：2009
卷号：106
期号：23
页码：9379-9384
DOI：10.1073/pnas.0900258106
语种：English
出版社：The National Academy of Sciences of the United States of America
摘要：Androgen receptor (AR) signaling regulates the development and homeostasis of male reproductive organs, including the prostate. Deregulation of AR and AR coregulators, expression, or activity is involved in the initiation of prostate cancer and contributes to the transition of the disease to hormone-refractory stage. The ubiquitous {beta}Arrestin proteins are now recognized as bona fide adapters and signal transducers with target effectors found in both the cytosol and nucleus. Here, we provide evidence that {beta}Arrestin2 forms a complex with AR and acts as an AR corepressor in androgen-dependent prostate cancer cells. Accordingly, the forced overexpression of {beta}Arrestin2 diminishes, and knockdown of {beta}Arrestin2 expression with RNAi increases the androgen-induced prostate-specific antigen (PSA) gene expression. {beta}Arrestin2 serves as an adapter, bringing into close proximity the Mdm2 E3 ligase and AR, thereby promoting AR ubiquitylation and degradation. Human prostate tissues evidence an inverse relationship between the expression of {beta}Arrestin2 and AR activity: glands that express high levels of {beta}Arrestin2 exhibit low expression of PSA, and those glands that express low levels of {beta}Arrestin2 evidence elevated PSA levels. We conclude that {beta}Arrestin2 acts as a corepressor of AR by serving as a scaffold for Mdm2 leading to the AR ubiquitylation and degradation.
