It's all in the combination: decoding the epigenome for cancer research and diagnostics

被引:6
|
作者
Furth, Noa [1 ]
Shema, Efrat [1 ]
机构
[1] Weizmann Inst Sci, Dept Biol Regulat, IL-76100 Rehovot, Israel
基金
欧洲研究理事会;
关键词
CELL-FREE DNA; HISTONE ACETYLATION DYNAMICS; CHROMATIN-STRUCTURE; SINGLE-MOLECULE; TRANSCRIPTION; LANDSCAPE; PLASMA; FAMILY; MARKS;
D O I
10.1016/j.gde.2022.101899
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Genome regulation is governed by the dynamics of chromatin modifications. The extensive and diverse array of DNA and histone modifications allow multiple elements to act outcomes. Yet, our ability to elucidate these complex combinations and link them to normal genome regulation, as well as understand their deregulation in cancer, has been hindered by the lack of suitable technologies. Here, we describe recent findings indicating the importance of the combinatorial epigenome, and novel methodologies to measure and characterize these combinations. These complementary methods span multiple disciplines, providing a means to decode epigenetic combinations and link them to biological outcomes. Finally, we discuss the promise of harnessing the rich combinatorial epigenetic information to improve cancer diagnostics and monitoring.
引用
收藏
页数:7
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