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雄激素受体与小窝蛋白-1在前列腺癌中的作用

Androgen receptor and caveolin-1 in prostate cancer.

作者信息

Bennett Nigel, Hooper John D, Lee C Soon, Gobe Glenda C

机构信息

UQCCR, School of Medicine, Faculty of Health Sciences, University of Queensland, Brisbane, QL, Australia.

出版信息

IUBMB Life. 2009 Oct;61(10):961-70. doi: 10.1002/iub.244.

Abstract

The androgen receptor (AR) is involved in the development and maintenance of the normal prostate and the development and progression of prostate cancer (PCa). Caveolin-1 (cav-1) is an AR co-regulator. The expression of this integral membrane protein is upregulated in PCa and correlates positively with its development. This review focuses on the likely interactive roles of AR and cav-1, with particular reference to progression to androgen-insensitivity in PCa. The classical role of AR is modulation of gene transcription by binding specific DNA sequences called androgen response elements in the promoter regions of target genes. To carry out this role, AR interacts with many co-regulator proteins which either enhance or repress its activation. Altered expression or misregulated activation of a co-regulator protein may significantly alter AR activity and the basal transcription rate of androgen responsive genes. Cav-1 has roles in cell signalling and trafficking, roles that are important in PCa survival, metastasis, and the development of multidrug resistant phenotypes. Although cav-1 appears to increase AR genomic activity and increase tumor cell survival, there is also mounting evidence that cav-1 can manipulate rapid, non-genomic AR signalling at the plasma membrane. By increasing our understanding of cav-1 as an AR co-regulator, we may be able to reinstate appropriate transcriptional responses to androgen signalling and minimise misregulated AR activity, thus permitting more effective targeted therapies for PCa.

摘要

雄激素受体(AR)参与正常前列腺的发育与维持以及前列腺癌(PCa)的发生和进展。小窝蛋白-1(cav-1)是一种AR共调节因子。这种整合膜蛋白的表达在PCa中上调,且与其发展呈正相关。本综述重点关注AR和cav-1可能的相互作用,特别是在PCa向雄激素不敏感进展方面。AR的经典作用是通过结合靶基因启动子区域中称为雄激素反应元件的特定DNA序列来调节基因转录。为了发挥这一作用,AR与许多共调节蛋白相互作用,这些蛋白要么增强要么抑制其激活。共调节蛋白表达的改变或激活失调可能会显著改变AR活性以及雄激素反应基因的基础转录速率。Cav-1在细胞信号传导和运输中发挥作用,这些作用在PCa的存活、转移以及多药耐药表型的发展中很重要。尽管cav-1似乎会增加AR的基因组活性并提高肿瘤细胞存活率,但也有越来越多的证据表明,cav-1可以在质膜上操纵快速的非基因组AR信号传导。通过增进我们对作为AR共调节因子的cav-1的理解,我们或许能够恢复对雄激素信号的适当转录反应,并将失调的AR活性降至最低,从而为PCa提供更有效的靶向治疗。

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