Histone acetylation and DNA methylation in ischemia/reperfusion injury.
Jinhua TangShougang ZhuangPublished in: Clinical science (London, England : 1979) (2019)
Ischemic/reperfusion (I/R) injury causes a series of serious clinical problems associated with high morbidity and mortality in various disorders, such as acute kidney injury (AKI), myocardial infarction, ischemic stroke, circulatory arrest, and peripheral vascular disease. The pathophysiology and pathogenesis of I/R injury is complex and multifactorial. Recent studies have revealed that epigenetic regulation is critically involved in the pathogenesis of I/R-induced tissue injury. In this review, we will sum up recent advances on the modification, regulation, and implication of histone modifications and DNA methylation in I/R injury-induced organ dysfunction. Understandings of I/R-induced epigenetic alterations and regulations will aid in the development of potential therapeutics.
Keyphrases
- dna methylation
- acute kidney injury
- ischemia reperfusion injury
- high glucose
- diabetic rats
- gene expression
- genome wide
- oxidative stress
- heart failure
- drug induced
- cardiac surgery
- mental health
- acute myocardial infarction
- risk assessment
- cell cycle
- cell proliferation
- left ventricular
- coronary artery disease
- single cell
- atrial fibrillation
- brain injury
- acute coronary syndrome