Epigenetic regulation of glucose metabolism

被引:8
|
作者
Sharma, Sapna [1 ,2 ]
Kriebel, Jennifer [1 ,2 ]
Grallert, Harald [1 ,2 ,3 ,4 ,5 ,6 ]
机构
[1] Helmholtz Zentrum Munchen, Inst Epidemiol 2, Res Unit Mol Epidemiol, Munich, Germany
[2] Helmholtz Zentrum Munchen, German Ctr Diabet Res DZD, Munich, Germany
[3] Helmholtz Zentrum Munchen, Clin Cooperat Grp Type Diabet 2, Munich, Germany
[4] Ludwig Maximillians Univ, Munich, Germany
[5] Helmholtz Zentrum Munchen, Clin Cooperat Grp Nutrigen & Type Diabet 2, Munich, Germany
[6] Tech Univ Munich, Munich, Germany
关键词
DNA methylation; epigenetics; glucose metabolism; histone modification; noncoding RNA; EPIGENOME-WIDE ASSOCIATION; TYPE-2; DIABETES-MELLITUS; LONG NONCODING RNA; DNA METHYLATION; INSULIN-RESISTANCE; PERIPHERAL-BLOOD; BIOMARKERS; SUSCEPTIBILITY; IDENTIFICATION; HYPERGLYCEMIA;
D O I
10.1097/MCO.0000000000000375
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Purpose of review Glucose metabolism is a central process in mammalian energy homeostasis. Its deregulation is a key factor in development of metabolic disease like diabetes and cancer. In recent decades, our understanding of gene regulation at the signaling, chromatin and posttranscriptional levels has seen dramatic developments. Recent findings A number of epigenetic mechanisms that do not affect the genetic code can be assessed with new technologies. However, increasing complexity becomes a major challenge for translation into clinical application. Summary The current review provides an update of transcriptional control of glucose metabolism, focusing on epigenetic regulators, DNA-methylation, histone modifications and noncoding RNAs. Recent studies heavily support the importance of those mechanisms for future therapeutics and preventive efforts for metabolic diseases.
引用
收藏
页码:266 / 271
页数:6
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