The Function and Therapeutic Potential of lncRNAs in Cardiac Fibrosis

Cardiac fibrosis remains an unresolved problem in cardiovascular diseases. Fibrosis of the myocardium plays a key role in the clinical outcomes of patients with heart injuries. Moderate fibrosis is favorable for cardiac structure maintaining and contractile force transmission, whereas adverse fibrosis generally progresses to ventricular remodeling and cardiac systolic or diastolic dysfunction. The molecular mechanisms involved in these processes are multifactorial and complex. Several molecular mechanisms, such as TGF-beta signaling pathway, extracellular matrix (ECM) synthesis and degradation, and non-coding RNAs, positively or negatively regulate myocardial fibrosis. Long noncoding RNAs (lncRNAs) have emerged as significant mediators in gene regulation in cardiovascular diseases. Recent studies have demonstrated that lncRNAs are crucial in genetic programming and gene expression during myocardial fibrosis. We summarize the function of lncRNAs in cardiac fibrosis and their contributions to miRNA expression, TGF-beta signaling, and ECMs synthesis, with a particular attention on the exosome-derived lncRNAs in the regulation of adverse fibrosis as well as the mode of action of lncRNAs secreted into exosomes. We also discuss how the current knowledge on lncRNAs can be applied to develop novel therapeutic strategies to prevent or reverse cardiac fibrosis.

Automated summary

Cardiac fibrosis is a significant issue in cardiovascular diseases, with molecular mechanisms involving TGF-beta signaling, extracellular matrix synthesis and degradation, and non-coding RNAs. Long noncoding RNAs play a crucial role in myocardial fibrosis and can regulate fibrosis by affecting miRNA expression, TGF-beta signaling, and ECM synthesis. Understanding these mechanisms can guide the development of novel therapeutic strategies to prevent or reverse cardiac fibrosis.