Triska Jeffrey, Mathew Christo, Zhao Yang, Chen Yuqing E, Birnbaum Yochai
Department of Medicine, Baylor College of Medicine, Houston, TX 77030, USA.
Cardiovascular Center, Department of Internal Medicine, University of Michigan Medical Center, Ann Arbor, MI 48109, USA.
J Clin Med. 2023 Jul 2;12(13):4446. doi: 10.3390/jcm12134446.
Much attention has been paid lately to harnessing the diagnostic and therapeutic potential of non-coding circular ribonucleic acids (circRNAs) and micro-RNAs (miRNAs) for the prevention and treatment of cardiovascular diseases. The genetic environment that contributes to atherosclerosis pathophysiology is immensely complex. Any potential therapeutic application of circRNAs must be assessed for risks, benefits, and off-target effects in both the short and long term. A search of the online PubMed database for publications related to circRNA and atherosclerosis from 2016 to 2022 was conducted. These studies were reviewed for their design, including methods for developing atherosclerosis and the effects of the corresponding atherosclerotic environment on circRNA expression. Investigated mechanisms were recorded, including associated miRNA, genes, and ultimate effects on cell mechanics, and inflammatory markers. The most investigated circRNAs were then further analyzed for redundant, disparate, and/or contradictory findings. Many disparate, opposing, and contradictory effects were observed across experiments. These include levels of the expression of a particular circRNA in atherosclerotic environments, attempted ascertainment of the in toto effects of circRNA or miRNA silencing on atherosclerosis progression, and off-target, cell-specific, and disease-specific effects. The high potential for detrimental and unpredictable off-target effects downstream of circRNA manipulation will likely render the practice of therapeutic targeting of circRNA or miRNA molecules not only complicated but perilous.
近年来,人们对利用非编码环状核糖核酸(circRNAs)和微小核糖核酸(miRNAs)的诊断和治疗潜力来预防和治疗心血管疾病给予了极大关注。导致动脉粥样硬化病理生理学的遗传环境极其复杂。必须对circRNAs的任何潜在治疗应用进行短期和长期的风险、益处及脱靶效应评估。我们在在线PubMed数据库中搜索了2016年至2022年期间与circRNA和动脉粥样硬化相关的出版物。对这些研究的设计进行了综述,包括动脉粥样硬化的形成方法以及相应动脉粥样硬化环境对circRNA表达的影响。记录了所研究的机制,包括相关的miRNA、基因以及对细胞力学和炎症标志物的最终影响。然后对研究最多的circRNAs进行进一步分析,以找出冗余、不同和/或相互矛盾的发现。在各个实验中观察到了许多不同、相反和相互矛盾的效应。这些包括特定circRNA在动脉粥样硬化环境中的表达水平、试图确定circRNA或miRNA沉默对动脉粥样硬化进展的总体影响,以及脱靶、细胞特异性和疾病特异性效应。circRNA操纵下游产生有害和不可预测的脱靶效应的可能性很高,这可能会使针对circRNA或miRNA分子的治疗不仅复杂而且危险。