Expression of RAC 3, a steroid hormone receptor co-activator in prostate cancer

V. J. Gnanapragasam, H. Y. Leung, A. S. Pulimood, D. E. Neal, C. N. Robson

Research output: Contribution to journalArticlepeer-review

165 Scopus citations

Abstract

RAC 3, one of the p160 family of co-activators is known to enhance the transcriptional activity of a number of steroid receptors. As co-activators are also known to enhance androgen receptor (AR) activity, we investigated the role of RAC 3 in the context of prostate cancer. In prostate cancer cell lines, we found variable levels of the RAC 3 protein with highest expression seen in AR-positive LNCaP cells, moderate expression in AR-negative PC 3 cells and low-level expression in AR-negative DU 145 cells. Immuno-precipitation studies showed that endogenous RAC 3 interacted with the AR in vivo and transfection assays confirmed that RAC 3 enhanced AR transcriptional activity. In clinical prostate tissue, we found strong RAC 3 mRNA expression and immuno-histochemistry demonstrated that in benign tissue, the protein was expressed predominantly in luminal cells, while in primary malignant epithelium it was more homogeneously expressed. In a series of 37 patients, the levels of RAC 3 expression correlated significantly with tumour grade (P = 0.01) and stage of disease (P = 0.03) but not with serum PSA levels. In addition moderate or high RAC 3 expression was associated with poorer disease-specific survival (P = 0.03). We conclude that RAC 3 is an important co-activator of the AR in the prostate and may have an important role in the progression of prostate cancer.

Original languageEnglish
Pages (from-to)1928-1936
Number of pages9
JournalBritish Journal of Cancer
Volume85
Issue number12
DOIs
StatePublished - 2001
Externally publishedYes

Keywords

  • Androgen receptor
  • Co-activator
  • Prostate cancer
  • RAC 3
  • Survival outcome

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