Abstract
Steroid receptor RNA activator (SRA) was first isolated as a steroid receptor co-activator that functioned as an RNA transcript. Later, we demonstrated that SRA needs to be translated in order to co-activate androgen receptor (AR). Here, we showed that three isoforms of human SRA enhanced AR activities. Small interfering RNA against SRA suppressed AR activities in PC-3 cells transfected with pSG5AR and in LNCaP cells that have an endogenous mutated-AR. Western blot showed that SRA protein was expressed at a higher level in PC-3 than in LNCaP cells, suggesting that SRA may be related to hormone-independent growth of prostate cancer. © 2006 Nature Publishing Group All rights reserved.
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Kurisu, T., Tanaka, T., Ishii, J., Matsumura, K., Sugimura, K., Nakatani, T., & Kawashima, H. (2006). Expression and function of human steroid receptor RNA activator in prostate cancer cells: Role of endogenous hSRA protein in androgen receptor-mediated transcription. Prostate Cancer and Prostatic Diseases, 9(2), 173–178. https://doi.org/10.1038/sj.pcan.4500867
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