Genome-wide analysis of androgen receptor binding and gene regulation in two CWR22-derived prostate cancer cell lines release_ztb5la3rpnexrjvsyyx4lcibbq

by Honglin Chen, Stephen J Libertini, Michael George, Satya Dandekar, Clifford G Tepper, Bushra Al-Bataina, Hsing-Jien Kung, Paramita M Ghosh, Maria Mudryj

Published in Endocrine-Related Cancer by Bioscientifica.

2010   Volume 17, p857-873

Abstract

Prostate carcinoma (CaP) is a heterogeneous multifocal disease where gene expression and regulation are altered not only with disease progression but also between metastatic lesions. The androgen receptor (AR) regulates the growth of metastatic CaPs; however, sensitivity to androgen ablation is short lived, yielding to emergence of castrate-resistant CaP (CRCaP). CRCaP prostate cancers continue to express the AR, a pivotal prostate regulator, but it is not known whether the AR targets similar or different genes in different castrate-resistant cells. In this study, we investigated AR binding and AR-dependent transcription in two related castrate-resistant cell lines derived from androgen-dependent CWR22-relapsed tumors: CWR22Rv1 (Rv1) and CWR-R1 (R1). Expression microarray analysis revealed that R1 and Rv1 cells had significantly different gene expression profiles individually and in response to androgen. In contrast, AR chromatin immunoprecipitation (ChIP) combined with promoter DNA microarrays (ChIP-on-chip) studies showed that they have a similar AR-binding profile. Coupling of the microarray study with ChIP-on-chip analysis identified direct AR targets. The most prominent function of transcripts that were direct AR targets was transcriptional regulation, although only one transcriptional regulator, CCAAT/enhancer binding protein δ, was commonly regulated in both lines. Our results indicate that the AR regulates the expression of different transcripts in the two lines, and demonstrate the versatility of the AR-regulated gene expression program in prostate tumors.
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Type  article-journal
Stage   published
Year   2010
DOI  10.1677/erc-10-0081
PubMed  20634343
PMC  PMC3539310
Wikidata  Q38342443
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