| Literature DB >> 19917249 |
John D Norris1, Ching-Yi Chang, Bryan M Wittmann, Rebecca S Kunder, Huaxia Cui, Daju Fan, James D Joseph, Donald P McDonnell.
Abstract
HOXB13 is a member of the homeodomain family of sequence-specific transcription factors and, together with the androgen receptor (AR), plays a critical role in the normal development of the prostate gland. We demonstrate here that, in prostate cancer cells, HOXB13 is a key determinant of the response to androgens. Specifically, it was determined that HOXB13 interacts with the DNA-binding domain of AR and inhibits the transcription of genes that contain an androgen-response element (ARE). In contrast, the AR:HOXB13 complex confers androgen responsiveness to promoters that contain a specific HOXB13-response element. Further, HOXB13 and AR synergize to enhance the transcription of genes that contain a HOX element juxtaposed to an ARE. The profound effects of HOXB13 knockdown on androgen-regulated proliferation, migration, and lipogenesis in prostate cancer cells highlight the importance of the observed changes in gene expression.Entities:
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Year: 2009 PMID: 19917249 PMCID: PMC2788777 DOI: 10.1016/j.molcel.2009.10.020
Source DB: PubMed Journal: Mol Cell ISSN: 1097-2765 Impact factor: 17.970