Unknown,Transcriptomics,Genomics,Proteomics

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Aberrant BAF57 Signaling Facilitates Pro-metastatic Phenotypes


ABSTRACT: BAF57, a component of the SWI/SNF chromatin remodeling complex conglomerate,modulates androgen receptor activity to promote prostate cancer. However the molecular consequences of tumor associated BAF57 elevation have remianed undefined in advanced disease such as castration resistant prostate cancer and/or metastasis Global gene expression analyses were performed in models mimicking tumor-associated BAF57 expression. These analyses demonstrated that BAF57 deregulation circumvented androgen mediated signaling and elicited upregulation of M-NM-12 integrin and other migration and metastasis related gene signatures. LNCaP cells were transfected to overexpress BAF57 and validated for BAF57 transcript induction. Appropriate vector control transfected cells were also used. Vector and BAF57 transfected samples were treated with 0.1% vehicle with a 1nM DHT vector control. Gene expression analyses were performed on biological duplicates.

ORGANISM(S): Homo sapiens

SUBMITTER: Adam Ertel 

PROVIDER: E-GEOD-44418 | biostudies-arrayexpress |

REPOSITORIES: biostudies-arrayexpress

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Aberrant BAF57 signaling facilitates prometastatic phenotypes.

Balasubramaniam Sucharitha S   Comstock Clay E S CE   Ertel Adam A   Jeong Kwang Won KW   Stallcup Michael R MR   Addya Sankar S   McCue Peter A PA   Ostrander William F WF   Augello Michael A MA   Knudsen Karen E KE  

Clinical cancer research : an official journal of the American Association for Cancer Research 20130314 10


<h4>Purpose</h4>BAF57, a component of the switching-defective and sucrose nonfermenting (SWI/SNF) chromatin-remodeling complex conglomerate, modulates androgen receptor activity to promote prostate cancer. However, the molecular consequences of tumor-associated BAF57 expression have remained undefined in advanced disease such as castration-resistant prostate cancer and/or metastasis.<h4>Experimental design</h4>Clinical human specimens of primary and metastatic prostate cancer were immunohistoche  ...[more]

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