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SGEF is overexpressed in prostate cancer and contributes to prostate cancer progression.
Wang, Hongtao; Wu, Ruiqin; Yu, Lan; Wu, Feima; Li, Shanhu; Zhao, Yali; Li, Hailiang; Luo, Guolan; Wang, Jian; Zhou, Jianguang.
Affiliation
  • Wang H; Laboratory of Medical Molecular Biology, Beijing Institute of Biotechnology, Beijing, PR China.
Oncol Rep ; 28(4): 1468-74, 2012 Oct.
Article in En | MEDLINE | ID: mdl-22824926
ABSTRACT
The purpose of this study was to investigate the potential roles of the SH3-containing guanine nucleotide exchange factor (SGEF) in human prostate cancer. Experimental data showed that SGEF was overexpressed in human prostate cancer cells and specimens. The reduction of SGEF expression through an SGEF-targeting siRNA in androgen-independent C4-2 and C4-2B cells suppressed both anchorage-dependent and anchorage-independent growth. In addition, the androgen receptor (AR) antagonist bicalutamide further strengthened this inhibitory effect due to the suppression of the elevated AR transactivation after knockdown of SGEF. Collectively, our results provide the first demonstration that SGEF is a novel promoter of human prostate cancer progression and development.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Prostatic Neoplasms / Guanine Nucleotide Exchange Factors Limits: Humans / Male Language: En Journal: Oncol Rep Journal subject: NEOPLASIAS Year: 2012 Document type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Prostatic Neoplasms / Guanine Nucleotide Exchange Factors Limits: Humans / Male Language: En Journal: Oncol Rep Journal subject: NEOPLASIAS Year: 2012 Document type: Article
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