Adjmi Matthew, Tse Isabelle, Zangi Lior
Cardiovascular Research Institute, Icahn School of Medicine at Mount Sinai, New York, New York 10029, USA.
Department of Genetics and Genomic Sciences, Icahn School of Medicine at Mount Sinai, New York, New York 10029, USA.
Cardiol Plus. 2025 Apr-Jun;10(2):117-128. doi: 10.1097/CP9.0000000000000118. Epub 2025 Jun 30.
As ischemic heart disease (IHD) remains the leading cause of mortality worldwide, there is an urgent need for innovative therapies that go beyond symptom management. The irreversible damage to cardiac tissue following myocardial infarction (MI) and the limited regenerative and proliferative capacity of adult cardiomyocytes (CMs) present significant challenges to the development of treatments capable of restoring cardiac function. This review focuses on emerging modified and non-modified messenger ribonucleic acid (mRNA)-based therapies, which offer targeted and transient protein expression. The studies reviewed here address three major therapeutic strategies: cardiac regeneration, aimed at inducing CM proliferation to restore lost cardiac muscle; cardiac protection, centered on anti-apoptotic and anti-inflammatory methods to mitigate further tissue damage; and cardiovascular regeneration, focused on promoting angiogenesis and restoring vascular integrity after injury. By examining mRNA and modified mRNA (modRNA) therapies across these three approaches, this review showcases mRNA's promising role in advancing muscular and vascular regenerative and protective therapeutics for IHD.
由于缺血性心脏病(IHD)仍是全球主要的死亡原因,因此迫切需要超越症状管理的创新疗法。心肌梗死(MI)后心脏组织的不可逆损伤以及成年心肌细胞(CMs)有限的再生和增殖能力,给能够恢复心脏功能的治疗方法的开发带来了重大挑战。本综述重点关注新兴的基于修饰和未修饰信使核糖核酸(mRNA)的疗法,这些疗法可实现靶向和瞬时蛋白表达。这里综述的研究涉及三种主要治疗策略:心脏再生,旨在诱导CM增殖以恢复丧失的心肌;心脏保护,以抗凋亡和抗炎方法为中心以减轻进一步的组织损伤;以及心血管再生,专注于促进血管生成和损伤后恢复血管完整性。通过研究这三种方法中的mRNA和修饰mRNA(modRNA)疗法,本综述展示了mRNA在推进针对IHD的肌肉和血管再生及保护疗法方面的前景。