학술논문

MicroRNAs in the regulation of cellular redox status and its implications in myocardial ischemia-reperfusion injury
Document Type
article
Source
Subject
Biological Sciences
Medicinal and Biomolecular Chemistry
Chemical Sciences
Biotechnology
Genetics
Cardiovascular
Heart Disease - Coronary Heart Disease
Heart Disease
Underpinning research
1.1 Normal biological development and functioning
Generic health relevance
Gene Expression Regulation
Humans
MicroRNAs
Myocardial Infarction
Myocardial Reperfusion Injury
Oxidation-Reduction
Oxidative Stress
Antioxidants
Biomarkers
microRNA
Myocardial ischemia-reperfusion injury
Oxidative stress
Proteasome
Redox signaling
Biochemistry and Cell Biology
Medical Biochemistry and Metabolomics
Pharmacology and Pharmaceutical Sciences
Biochemistry and cell biology
Medicinal and biomolecular chemistry
Language
Abstract
MicroRNAs (miRNAs) are small RNAs that do not encode for proteins and play key roles in the regulation of gene expression. miRNAs are involved in a comprehensive range of biological processes such as cell cycle control, apoptosis, and several developmental and physiological processes. Oxidative stress can affect the expression levels of multiple miRNAs and, conversely, miRNAs may regulate the expression of redox sensors, alter critical components of the cellular antioxidants, interact with the proteasome, and affect DNA repair systems. The number of publications identifying redox-sensitive miRNAs has increased significantly over the last few years, and some miRNA targets such as Nrf2, SIRT1 and NF-κB have been identified. The complex interplay between miRNAs and ROS is discussed together with their role in myocardial ischemia-reperfusion injury and the potential use of circulating miRNAs as biomarkers of myocardial infarction. Detailed knowledge of redox-sensitive miRNAs is needed to be able to effectively use individual compounds or sets of miRNA-modulating compounds to improve the health-related outcomes associated with different diseases.