Boen Hanne M, Cherubin Martina, Franssen Constantijn, Gevaert Andreas B, Witvrouwen Isabel, Bosman Matthias, Guns Pieter-Jan, Heidbuchel Hein, Loeys Bart, Alaerts Maaike, Van Craenenbroeck Emeline M
Research Group Cardiovascular Diseases, GENCOR, University of Antwerp, Antwerp, Belgium.
Department of Cardiology, Antwerp University Hospital, Antwerp, Belgium.
JACC CardioOncol. 2024 Feb 27;6(2):183-199. doi: 10.1016/j.jaccao.2023.12.009. eCollection 2024 Apr.
Close monitoring for cardiotoxicity during anthracycline chemotherapy is crucial for early diagnosis and therapy guidance. Currently, monitoring relies on cardiac imaging and serial measurement of cardiac biomarkers like cardiac troponin and natriuretic peptides. However, these conventional biomarkers are nonspecific indicators of cardiac damage. Exploring new, more specific biomarkers with a clear link to the underlying pathomechanism of cardiotoxicity holds promise for increased specificity and sensitivity in detecting early anthracycline-induced cardiotoxicity. miRNAs (microRNAs), small single-stranded, noncoding RNA sequences involved in epigenetic regulation, influence various physiological and pathological processes by targeting expression and translation. Emerging as new biomarker candidates, circulating miRNAs exhibit resistance to degradation and offer a direct pathomechanistic link. This review comprehensively outlines their potential as early biomarkers for cardiotoxicity and their pathomechanistic link.
在蒽环类化疗期间密切监测心脏毒性对于早期诊断和治疗指导至关重要。目前,监测依赖于心脏成像以及对心脏生物标志物(如心肌肌钙蛋白和利钠肽)的系列测量。然而,这些传统生物标志物是心脏损伤的非特异性指标。探索与心脏毒性潜在发病机制有明确联系的新的、更具特异性的生物标志物,有望提高检测早期蒽环类药物诱导的心脏毒性的特异性和敏感性。微小RNA(miRNAs)是参与表观遗传调控的小单链非编码RNA序列,通过靶向表达和翻译影响各种生理和病理过程。作为新的生物标志物候选物出现的循环miRNAs表现出抗降解性,并提供了直接的发病机制联系。本综述全面概述了它们作为心脏毒性早期生物标志物的潜力及其发病机制联系。