The role of histone deacetylases in prostate cancer

被引:117
作者
Abbas, Ata [1 ,2 ]
Gupta, Sanjay [1 ,2 ,3 ]
机构
[1] Case Western Reserve Univ, Dept Urol, Cleveland, OH 44106 USA
[2] Univ Hosp Case Med Ctr, Cleveland, OH USA
[3] Case Comprehens Canc Ctr, Cleveland, OH USA
关键词
prostate cancer; histone deacetylases; apoptosis; growth arrest; epigenetics; histone modification; acetylation;
D O I
10.4161/epi.3.6.7273
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Epigenetic modifications play a key role in the patho-physiology of prostate cancer. Histone deacetylases (HDACs) play major roles in prostate cancer progression. HDACs are part of a transcriptional co-repressor complex that influences various tumor suppressor genes. Because of the significant roles played by HDACs in various human cancers, HDAC inhibitors are emerging as a new class of chemotherapeutic agents. HDAC inhibitors have been shown to induce cell growth arrest, differentiation and/or apoptosis in prostate cancer. The combined use of HDAC inhibitors with other chemotherapeutic agents or radiotherapy in cancer treatment has shown promising results. Various HDAC inhibitors are in different stages of clinical trials. In this review, we discuss the molecular mechanism(s) through which HDACs influence prostate cancer progression and the potential roles of HDAC inhibitors in prostate cancer prevention and therapy.
引用
收藏
页码:300 / 309
页数:10
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