Sequencing the transcriptional network of androgen receptor in prostate cancer

被引:9
作者
Chng, Kern Rei [1 ,4 ]
Cheung, Edwin [1 ,2 ,3 ]
机构
[1] ASTAR, Canc Biol & Pharmacol, Genome Inst Singapore, Singapore 138672, Singapore
[2] Natl Univ Singapore, Yong Loo Lin Sch Med, Dept Biochem, Singapore 117597, Singapore
[3] Nanyang Technol Univ, Sch Biol Sci, Singapore 637551, Singapore
[4] Natl Univ Singapore, Grad Sch Integrat Sci & Engn, Singapore 117573, Singapore
关键词
Chromatin immunoprecipitation; High-throughput sequencing; Androgen receptor; Prostate cancer; Transcriptional network; GROUP PROTEIN EZH2; HISTONE DEACETYLASE-1; GENE FUSIONS; E-CADHERIN; MESENCHYMAL TRANSITION; EXPRESSION; POLYCOMB; BINDING; PROGRESSION; ACTIVATION;
D O I
10.1016/j.canlet.2012.11.009
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The progression of prostate cancer is largely dependent on the activity of the androgen receptor (AR), which in turn, correlates with the net output of the AR transcriptional regulatory network. A detailed and thorough understanding of the AR transcriptional regulatory network is therefore critical in the strategic manipulation of AR activity for the targeted eradication of prostate cancer cells. In this mini-review, we highlight some of the novel and unexpected mechanistic and functional insights of the AR transcriptional network derived from recent targeted sequencing (ChIP-Seq) studies of AR and its coregulatory factors in prostate cancer cells. (C) 2012 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:254 / 260
页数:7
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