Targeting the cancer epigenome for therapy

被引:846
作者
Jones, Peter A. [1 ]
Issa, Jean-Pierre J. [2 ]
Baylin, Stephen [1 ,3 ]
机构
[1] Van Andel Res Inst, Grand Rapids, MI 49503 USA
[2] Temple Univ, Lewis Katz Sch Med, Fels Inst Canc Res, Philadelphia, PA 19140 USA
[3] Johns Hopkins, Sidney Kimmel Comprehens Canc Ctr, Dept Oncol, Baltimore, MD 21287 USA
基金
美国国家卫生研究院;
关键词
HISTONE DEACETYLASE INHIBITORS; RISK MYELODYSPLASTIC SYNDROME; TUMOR-SUPPRESSOR GENES; ACUTE MYELOID-LEUKEMIA; CELL LUNG-CANCER; DNA METHYLATION; TET2; MUTATIONS; 5-AZA-2'-DEOXYCYTIDINE DECITABINE; HYPOMETHYLATING AGENT; SELECTIVE-INHIBITION;
D O I
10.1038/nrg.2016.93
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Next-generation sequencing has revealed that more than 50% of human cancers harbour mutations in enzymes that are involved in chromatin organization. Tumour cells not only are activated by genetic and epigenetic alterations, but also routinely use epigenetic processes to ensure their escape from chemotherapy and host immune surveillance. Hence, a growing emphasis of recent drug discovery efforts has been on targeting the epigenome, including DNA methylation and histone modifications, with several new drugs being tested and some already approved by the US Food and Drug Administration (FDA). The future will see the increasing success of combining epigenetic drugs with other therapies. As epigenetic drugs target the epigenome as a whole, these true 'genomic medicines' lessen the need for precision approaches to individualized therapies.
引用
收藏
页码:630 / 641
页数:12
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