Epigenetic modulators as therapeutic targets in prostate cancer

被引:0
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作者
Inês Graça
Eva Pereira-Silva
Rui Henrique
Graham Packham
Simon J. Crabb
Carmen Jerónimo
机构
[1] Cancer Biology and Epigenetics Group—Research Center (CI-IPOP),School of Allied Health Sciences (ESTSP)
[2] Portuguese Oncology Institute of Porto (IPO-Porto),Department of Pathology
[3] Polytechnic of Porto,Department of Pathology and Molecular Immunology
[4] Portuguese Oncology Institute of Porto (IPO Porto),Cancer Research UK Centre, Cancer Sciences, The Somers Cancer Research Building
[5] Institute of Biomedical Sciences Abel Salazar—University of Porto (ICBAS-UP),undefined
[6] University of Southampton Faculty of Medicine,undefined
[7] Southampton General Hospital,undefined
来源
Clinical Epigenetics | 2016年 / 8卷
关键词
Prostate cancer; DNMTi; Histone modulators;
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学科分类号
摘要
Prostate cancer is one of the most common non-cutaneous malignancies among men worldwide. Epigenetic aberrations, including changes in DNA methylation patterns and/or histone modifications, are key drivers of prostate carcinogenesis. These epigenetic defects might be due to deregulated function and/or expression of the epigenetic machinery, affecting the expression of several important genes. Remarkably, epigenetic modifications are reversible and numerous compounds that target the epigenetic enzymes and regulatory proteins were reported to be effective in cancer growth control. In fact, some of these drugs are already being tested in clinical trials. This review discusses the most important epigenetic alterations in prostate cancer, highlighting the role of epigenetic modulating compounds in pre-clinical and clinical trials as potential therapeutic agents for prostate cancer management.
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