Epigenetic drift, epigenetic clocks and cancer risk

被引:87
作者
Zheng, Shijie C. [1 ,2 ]
Widschwendter, Martin [3 ]
Teschendorff, Andrew E. [1 ,3 ,4 ]
机构
[1] Chinese Acad Sci, Shanghai Inst Biol Sci, CAS MPG Partner Inst Computat Biol, CAS Key Lab Computat Biol, Shanghai 200031, Peoples R China
[2] Univ Chinese Acad Sci, 19A Yuquan Rd, Beijing 100049, Peoples R China
[3] UCL, Dept Womens Canc, 74 Huntley St, London WC1E 6AU, England
[4] UCL, UCL Canc Inst, Stat Canc Genom, 72 Huntley St, London WC1E 6BT, England
关键词
aging; cancer; cancer risk; DNA methylation; epigenetic; epigenetic clock; DNA METHYLATION CHANGES; EPIGENOME-WIDE ASSOCIATION; DETECTABLE CLONAL MOSAICISM; SOMATIC MUTATIONS; PERIPHERAL-BLOOD; LUNG-CANCER; STEM-CELLS; AGE; GENES; HYPERMETHYLATION;
D O I
10.2217/epi-2015-0017
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
It is well-established that the DNA methylation landscape of normal cells undergoes a gradual modification with age, termed as 'epigenetic drift'. Here, we review the current state of knowledge of epigenetic drift and its potential role in cancer etiology. We propose a new terminology to help distinguish the different components of epigenetic drift, with the aim of clarifying the role of the epigenetic clock, mitotic clocks and active changes, which accumulate in response to environmental disease risk factors. We further highlight the growing evidence that epigenetic changes associated with cancer risk factors may play an important causal role in cancer development, and that monitoring these molecular changes in normal cells may offer novel risk prediction and disease prevention strategies.
引用
收藏
页码:705 / 719
页数:15
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