Journal
INTERNATIONAL JOURNAL OF CANCER
Volume 123, Issue 12, Pages 2774-2781Publisher
WILEY
DOI: 10.1002/ijc.23885
Keywords
ERG; HDAC inhibitors; prostate cancer; AR
Categories
Funding
- EU-EPITRON [LSHC-CT-2005-518417]
- EU-PRIMA [LSHC-CT_204504587]
- Marie Curie Canceromics [MEXT-CT-2003-2728]
- Academy of Finland
- Cancer Organizations Finland
- Sigrid Juselius Foundation
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TMPRSS2 gene and oncogenic ETS factors, such as ERG, occur in up to 50% of all prostate cancers. We recently defined a gene signature that was characteristic to prostate cancers with ERG activation. This suggested epigenetic reprogramming, such as upregulation of histone deactylase 1 (HDAC1) gene and downregulation of its target genes. We then hypothesized that patients with ERG-positive prostate cancers may benefit from epigenetic therapy such as HDAC inhibition (HDACi), especially in combination with antiandrogens. Here, we exposed ERG-positive prostate cancer cell lines to HDAC inhibitors Trichostatin A (TSA), MS-275 and suberoylanilide hydroxamic acid (SAHA) with or without androgen deprivation. We explored the effects on cell phenotype, gene expression as well as ERG and androgen receptor (AR) signaling. When compared with 5 other prostate cell lines, ERG-positive VCaP and DuCap cells were extremely sensitive to HDACi, in particular TSA, showing synergy, with concomitant androgen deprivation increasing apoptosis. Both of the HDAC inhibitors studied caused repression of the ERG-fusion gene, whereas the pan-HDAC inhibitor TSA prominently, repressed the ERG-associated gene signature. Additionally, HDACi and flutamide caused retention of AR in the cytoplasm, indicating blockage of androgen signaling. Our results support the hypothesis that HDACi, especially in combination with androgen deprivation, is effective against TMPRSS2-ERG-fusion positive prostate cancer ill vitro. Together with our previous in vivo observations of an epigenetic reprogramming gene signature in clinical ERG-positive prostate cancers, these studies provide mechanistic insights to ERG-associated tumorigenesis and suggest therapeutic paradigms to be tested in vivo. (C) 2008 Wiley-Liss, Inc.
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