Key result
Subcellular noncoding RNAs offer novel targeted therapeutic avenues for heart failure management.
Why the study?
Mortality from heart failure remains high despite advanced therapies, creating an urgent need for novel targets and therapeutic strategies.
Subcellular localization of non-coding RNAs is a key determinant of their molecular function and a critical factor for optimizing RNA-based therapies in heart failure.
Subcellular ncRNA localization may refine RNA therapeutic design in heart failure; hypothesis-generating and leaves clinical translation open pending targeted trials.
Cardiovascular diseases remain the leading causes of mortality and disability, with heart failure being the end stage of various cardiovascular diseases. The well-established biological pathogenesis of heart failure includes cardiomyocyte hypertrophy, cardiac fibrosis, and endothelial dysfunction. Despite advanced therapies, mortality from heart failure remains high. Therefore, novel targets and therapeutic strategies for heart failure are urgently needed. The discovery of microRNAs (miRNAs) and long non-coding RNAs (lncRNAs) extends understanding of the pathophysiological mechanisms of diseases and provides new perspectives on potential clinical applications. Emerging evidence shows that miRNAs and lncRNAs may be located in different subcellular fractions and possess various regulatory functions; this deepens the understanding of miRNA and lncRNA functions. Furthermore, miRNA- or lncRNA-based therapies may be optimized based on their subcellular functions. In this review, we have summarized the diverse functions of subcellular miRNAs and lncRNAs and the current clinical applications of miRNAs and lncRNAs in the treatment of heart failure.
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Tang et al. (2026) conducted a review in Heart failure. microRNAs and long noncoding RNAs was evaluated. Subcellular microRNAs and long noncoding RNAs possess diverse regulatory functions that offer novel perspectives for targeted therapeutic applications in heart failure.
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