| Literature DB >> 25158280 |
Liang Cui1, Mingyang Li2, Fan Feng3, Yutao Yang4, Xingyi Hang5, Jiajun Cui6, Jiangping Gao7.
Abstract
The androgen receptor (AR) plays critical roles in human prostate carcinoma progression and transformation. However, the activation of AR is regulated by co-regulators. MEIS1 protein, the homeodomain transcription factor, exhibited a decreased level in poor-prognosis prostate tumors. In this study, we investigated a potential interaction between MEIS1 and AR. We found that overexpression of MEIS1 inhibited the AR transcriptional activity and reduced the expression of AR target gene. A potential protein-protein interaction between AR and MEIS1 was identified by the immunoprecipitation and GST pull-down assays. Furthermore, MEIS1 modulated AR cytoplasm/nucleus translocation and the recruitment to androgen response element in prostate specific antigen (PSA) gene promoter sequences. In addition, MEIS1 promoted the recruitment of NCoR and SMRT in the presence of R1881. Finally, MEIS1 inhibited the proliferation and anchor-independent growth of LNCaP cells. Taken together, our data suggests that MEIS1 functions as a novel AR co-repressor.Entities:
Keywords: Androgen; Androgen receptor; Gene expression; MEIS1; Physical protein interaction; Prostatic carcinoma; Transcriptional activity
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Year: 2014 PMID: 25158280 DOI: 10.1016/j.yexcr.2014.08.023
Source DB: PubMed Journal: Exp Cell Res ISSN: 0014-4827 Impact factor: 3.905