Oncohistone Mutations in Diffuse Intrinsic Pontine Glioma

被引:17
|
作者
Zhang, Xu [1 ,2 ,3 ]
Zhang, Zhiguo [1 ,2 ,3 ]
机构
[1] Columbia Univ, Irving Med Ctr, Inst Canc Genet, New York, NY 10032 USA
[2] Columbia Univ, Irving Med Ctr, Dept Pediat, New York, NY 10032 USA
[3] Columbia Univ, Irving Med Ctr, Dept Genet & Dev, New York, NY 10032 USA
来源
TRENDS IN CANCER | 2019年 / 5卷 / 12期
关键词
PEDIATRIC HIGH-GRADE; HISTONE METHYLTRANSFERASE ACTIVITY; POTENTIAL THERAPEUTIC TARGET; H3.3K27M MUTATION; DRIVER MUTATIONS; POLYCOMB; METHYLATION; DNA; INHIBITION; COMPLEX;
D O I
10.1016/j.trecan.2019.10.009
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Diffuse intrinsic pontine glioma (DIPG) is a lethal pediatric tumor with no currently available treatment options. More than 60-70% DIPGtumors harbor heterozygous mutations at genes encoding histone H3 proteins that replace lysine 27 with methionine (K27M). In this review, we discuss how K27M mutation reprograms the cancer epigenome to lead to tumorigenesis, and highlight potential drug targets and therapeutic agents for DIPG.
引用
收藏
页码:799 / 808
页数:10
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