Epigenetic reprogramming in metabolic disorders: nutritional factors and beyond

被引:77
作者
Cheng, Zhiyong [1 ]
Zheng, Louise [1 ]
Almeida, Fabio A. [2 ]
机构
[1] Virginia Tech, Coll Agr & Life Sci, Fralin Translat Obes Res Ctr, Dept Human Nutr Foods & Exercise, Blacksburg, VA 24061 USA
[2] Univ Nebraska Med Ctr, Coll Publ Hlth, Dept Hlth Promot Social & Behav Hlth, Omaha, NE 68198 USA
基金
美国食品与农业研究所;
关键词
Epigenetic marker; DNA methylation; Reprogramming; Metabolic disorders; Intervention; EPIGENOME-WIDE ASSOCIATION; BODY-MASS INDEX; HUMAN ADIPOSE-TISSUE; DIFFERENTIAL DNA METHYLATION; MESSENGER-RNA EXPRESSION; TYPE-2; DIABETES-MELLITUS; FATTY LIVER-DISEASE; INSULIN-RESISTANCE; WEIGHT-LOSS; PROMOTER METHYLATION;
D O I
10.1016/j.jnutbio.2017.10.004
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Environmental factors (e.g., malnutrition and physical inactivity) contribute largely to metabolic disorders including obesity, type 2 diabetes, cardiometabolic disease and nonalcoholic fatty liver diseases. The abnormalities in metabolic activity and pathways have been increasingly associated with altered DNA methylation, histone modification and noncoding RNA5, whereas lifestyle interventions targeting diet and physical activity can reverse the epigenetic and metabolic changes. Here we review recent evidence primarily from human studies that links DNA methylation reprogramming to metabolic derangements or improvements, with a focus on cross-tissue (e.g., the liver, skeletal muscle, pancreas, adipose tissue and blood samples) epigenetic markers, mechanistic mediators of the epigenetic reprogramming, and the potential of using epigenetic traits to predict disease risk and intervention response. The challenges in epigenetic studies addressing the mechanisms of metabolic diseases and future directions are also discussed and prospected. (C) 2017 Elsevier Inc. All rights reserved.
引用
收藏
页码:1 / 10
页数:10
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