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Review Article | Open Access

Epigenetic regulation of prostate cancer

Ruixin Wanga,b( )Xiaoqi Liub,c
Department of Biochemistry, Purdue University, West Lafayette, IN, 47907, USA
Department of Toxicology and Cancer Biology, University of Kentucky, Lexington, KY, 40536, USA
Markey Cancer Center, University of Kentucky, Lexington, KY, 40536, USA

Peer review under responsibility of Chongqing Medical University.

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Abstract

Prostate cancer is (PCa) the second leading cause of cancer death in males in the United State, with 174,650 new cases and 31,620 deaths estimated in 2019. It has been documented that epigenetic deregulation such as histone modification and DNA methylation contributes to PCa initiation and progression. EZH2 (enhancer of zeste homolog 2), the catalytic subunit of the Polycomb Repressive Complex (PRC2) responsible for H3K27me3 and gene repression, has been identified as a promising target in PCa. In addition, overexpression of other epigenetic regulators such as DNA methyltransferases (DNMT) is also observed in PCa. These epigenetic regulators undergo extensive post-translational modifications, in particular, phosphorylation. AKT, CDKs, PLK1, PKA, ATR and DNA-PK are the established kinases responsible for phosphorylation of various epigenetic regulators.

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Genes & Diseases
Pages 606-613

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Cite this article:
Wang R, Liu X. Epigenetic regulation of prostate cancer. Genes & Diseases, 2020, 7(4): 606-613. https://doi.org/10.1016/j.gendis.2019.10.018

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Received: 11 March 2019
Revised: 16 October 2019
Accepted: 30 October 2019
Published: 09 November 2019
© 2019, Chongqing Medical University.

This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).