Abolhasani Sakhavat, Ahmadi Yasin, Fattahi Davood, Rostami Yavar, Chollou Khalil Maleki
Department of Basic Sciences and Health, Sarab Faculty of Medical Sciences, Sarab, East Azerbaijan, Iran.
Department of Medical Laboratory Science, Komar University of Science and Technology, Sulaymaniyah, Kurdistan Region, Iraq.
J Clin Lab Anal. 2025 May;39(9):e70017. doi: 10.1002/jcla.70017. Epub 2025 Apr 4.
Cardiovascular diseases (CVDs) are the leading cause of mortality globally, often linked to oxidative stress. MicroRNAs (miRNAs) have emerged as significant regulators of oxidative stress within the cardiovascular system.
This review examines the complex relationship between miRNAs and oxidative stress, clarifying their effects on gene expression pathways related to ROS production and detoxification in CVDs.
From August to October 2024, we conducted a comprehensive search of PubMed, Scopus, Web of Science, and Google Scholar for studies published between 2014 and 2024 investigating the role of miRNAs in oxidative stress and cardiovascular diseases.
Specific miRNAs have been identified as critical regulators in the pathophysiology of CVDs, with distinct expression patterns correlated with conditions such as hypertension, coronary artery disease, and heart failure. For instance, miR-21 exacerbates oxidative stress by targeting genes essential for redox homeostasis, while miR-210 promotes endothelial cell survival under hypoxic conditions by mitigating ROS levels.
The reciprocal relationship between miRNAs and oxidative stress highlights the potential for therapeutic interventions targeting miRNA expression and activity in managing CVDs. Understanding these molecular mechanisms is vital for developing innovative strategies to address oxidative damage in cardiac tissues and improve cardiovascular health outcomes.
心血管疾病(CVDs)是全球主要的死亡原因,常与氧化应激相关。微小RNA(miRNAs)已成为心血管系统中氧化应激的重要调节因子。
本综述探讨miRNAs与氧化应激之间的复杂关系,阐明它们对CVDs中与活性氧(ROS)产生和解毒相关的基因表达途径的影响。
2024年8月至10月,我们对PubMed、Scopus、科学网和谷歌学术进行了全面检索,以查找2014年至2024年期间发表的研究miRNAs在氧化应激和心血管疾病中作用的文献。
特定的miRNAs已被确定为CVDs病理生理学中的关键调节因子,其独特的表达模式与高血压、冠状动脉疾病和心力衰竭等病症相关。例如,miR-21通过靶向氧化还原稳态所必需的基因加剧氧化应激,而miR-210通过降低ROS水平在缺氧条件下促进内皮细胞存活。
miRNAs与氧化应激之间的相互关系突出了针对miRNA表达和活性进行治疗干预以管理CVDs的潜力。了解这些分子机制对于制定创新策略以解决心脏组织中的氧化损伤并改善心血管健康结果至关重要。