Identification of transcription factors associated with castration‐resistance: Is the serum responsive factor a potential therapeutic target?. Issue 7 (28th January 2013)

• Record Type: Journal Article
• Authors: Prencipe, Maria; Madden, Stephen F.; O'Neill, Amanda; O'Hurley, Gillian; Culhane, Aedin; O'Connor, Darran; Klocker, Helmut; Kay, Elaine W.; Gallagher, William M.; Watson, William R.
• Is Part Of: Prostate. Volume 73:Issue 7(2013)
• Page Start: 743
• Page End: 753
• Publication Date: 2013-01-28
• Subjects: advanced prostate cancer -- transcription‐factors prediction analysis -- serum response factor (SRF); Prostate -- Diseases -- Periodicals; 616
• DOI: 10.1002/pros.22618
• Languages: English
• ISSNs: 0270-4137

Abstract

Abstract: BACKGROUND: Advanced prostate cancer is treated by hormone ablation therapy. However, despite an initial response, the majority of men relapse to develop castration‐resistant disease for which there are no effective treatments. We have previously shown that manipulating individual proteins has only minor alterations on the resistant phenotype so we hypothesize that targeting the central transcription factors (TFs) would represent a better therapeutic approach. METHODS: We have undertaken a transcriptomic analysis of gene expression differences between the androgen‐dependent LNCaP parental cells and its castration‐resistant Abl and Hof sublines, revealing 1, 660 genes associated with castration‐resistance. Using effective bioinformatic techniques, these transcriptomic data were integrated with TF binding sites resulting in a list of TFs associated with the differential gene expression observed. RESULTS: Following validation of the gene‐chip results, the serum response factor (SRF) was chosen for clinical validation and functional analysis due to its recent association with prostate cancer progression. SRF immunoreactivity in prostate tumor samples was shown for the first time to be associated with castration‐resistance. SRF inhibition by siRNA and the small molecule inhibitor CCG‐1423 resulted in decreased proliferation. CONCLUSION: SRF is a key TF by which resistant cells survive with depleted levels of androgens representing a target for therapeutic manipulation. Prostate 73: 743–753, 2013. © 2013 Wiley Periodicals, Inc.