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Epigenetic modulation in the treatment of atherosclerotic disease
被引:27
作者:

不详
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机构: Department of Clinical Medicine and Institute of Molecular Medicine, Trinity Centre for Health Sciences, St. James's Hospital, Dublin
机构:
[1] Department of Clinical Medicine and Institute of Molecular Medicine, Trinity Centre for Health Sciences, St. James's Hospital, Dublin
[2] Department of Cardiology, St. James's Hospital, Dublin
关键词:
SMOOTH-MUSCLE-CELLS;
LONG NONCODING RNAS;
DNA METHYLATION;
PROTOCATECHUIC ALDEHYDE;
UP-REGULATION;
HOMOCYSTEINE METABOLISM;
SENSITIVE MICRORNAS;
LEUKOCYTE ADHESION;
PLAQUE INSTABILITY;
NRF2;
EXPRESSION;
D O I:
10.3389/fgene.2014.00364
中图分类号:
Q3 [遗传学];
学科分类号:
071007 ;
090102 ;
摘要:
Cardiovascular disease is the single largest cause of death in the western world and its incidence is on the rise globally. Atherosclerosis, characterized by the development of atheromatus plaque, can trigger luminal narrowing and upon rupture result in myocardial infarction or ischemic stroke. Epigenetic phenomena are a focus of considerable research interest due to the role they play in gene regulation. Epigenetic mechanisms such as DNA methylation and histone acetylation have been identified as potential drug targets in the treatment of cardiovascular disease. miRNAs are known to play a role in gene silencing, which has been widely investigated in cancer. In comparison, the role they play in cardiovascular disease and plaque rupture is not well understood. Nutritional epigenetic modifiers from dietary components, for instance sulforaphane found in broccoli, have been shown to suppress the pro-inflammatory response through transcription factor activation. This review will discuss current and potential epigenetic therapeutics for the treatment of cardiovascular disease, focusing on the use of miRNAs and dietary supplements such as sulforaphane and protocatechuic aldehyde.
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