Fang Shengwei, Ainsworth Thomas, Zhang Peipei
Department of Nuclear Medicine, Hangzhou Cancer Hospital, Hangzhou, 310002, China.
Department of Emergency Medicine and Integrative Biosciences Center, Wayne State University, Detroit, MI, USA.
Curr Probl Cardiol. 2025 Sep;50(9):103106. doi: 10.1016/j.cpcardiol.2025.103106. Epub 2025 Jun 13.
Doxorubicin (DOX) remains a cornerstone chemotherapeutic agent despite its dose-dependent cardiotoxicity that can progress to irreversible dilated cardiomyopathy. At the same time, the mechanisms of DOX-induced cardiac injury are multifactorial, emerging evidence highlights circular RNAs (circRNAs) a unique class of covalently closed non-coding RNA molecules, as critical regulators of DOX cardiotoxicity. This review comprehensively examines the biogenesis and functional repertoire of circRNAs and their pivotal role in modulating DOX-induced cardiac damage. CircRNAs exert cardioprotective or cardiotoxic effects primarily through competitive endogenous RNA activity, RNA-binding protein interactions, translational products, and RNA N6-adenosine methylation-related mechanisms. Notably, the research gap lies in understanding how circRNAs orchestrate the complex interplay between five major regulated cell death pathways triggered by DOX: apoptosis, autophagy, necroptosis, ferroptosis, and pyroptosis. Additionally, circRNAs influence cellular processes underlying DOX-induced cardiomyocyte dysfunction, including oxidative stress, calcium handling defects, myocardial atrophy, thrombosis, and premature senescence. The novelty of this review lies in synthesizing evidence on circRNA-mediated regulatory networks across these diverse pathophysiological mechanisms, providing a theoretical foundation for developing circRNA-based diagnostic biomarkers and therapeutic interventions. Future research directions should focus on elucidating additional molecular mechanisms, validating circRNA-based biomarkers, and establishing translational frameworks for clinical applications to mitigate DOX cardiotoxicity while preserving its antitumor efficacy.
尽管阿霉素(DOX)存在剂量依赖性心脏毒性,可发展为不可逆的扩张型心肌病,但它仍然是一种基石性化疗药物。同时,DOX诱导心脏损伤的机制是多因素的,新出现的证据表明,环状RNA(circRNA)作为一类独特的共价闭合非编码RNA分子,是DOX心脏毒性的关键调节因子。本综述全面研究了circRNA的生物发生和功能谱及其在调节DOX诱导的心脏损伤中的关键作用。CircRNA主要通过竞争性内源RNA活性、RNA结合蛋白相互作用、翻译产物和RNA N6-腺苷甲基化相关机制发挥心脏保护或心脏毒性作用。值得注意的是,研究差距在于了解circRNA如何协调由DOX触发的五种主要调节性细胞死亡途径之间的复杂相互作用:凋亡、自噬、坏死性凋亡、铁死亡和焦亡。此外,circRNA影响DOX诱导的心肌细胞功能障碍的细胞过程,包括氧化应激、钙处理缺陷、心肌萎缩、血栓形成和早衰。本综述的新颖之处在于综合了关于circRNA介导的跨这些不同病理生理机制的调控网络的证据,为开发基于circRNA的诊断生物标志物和治疗干预措施提供了理论基础。未来的研究方向应集中在阐明更多分子机制、验证基于circRNA的生物标志物以及建立临床应用的转化框架,以减轻DOX的心脏毒性,同时保留其抗肿瘤疗效。