Key result
Site-directed RNA editing represents a novel, programmable, and reversible therapeutic approach with significant potential for treating cardiovascular diseases by correcting pathogenic point mutations.
Why the study?
Despite existing pharmacological and interventional treatments, cardiovascular disease cases continue to rise, highlighting the need for novel therapeutic strategies such as RNA editing to precisely and efficiently combat heart disease.
RNA editing therapeutics represent a novel and emerging strategy for the treatment of cardiovascular disease.
RNA editing may enable precision CVD therapies; leaves open clinical translation pending targeted trials.
Cardiovascular disease still remains the leading cause of morbidity and mortality worldwide. Current pharmacological or interventional treatments help to tackle symptoms and even reduce mortality, but cardiovascular disease cases continue to rise. The emergence of novel therapeutic strategies that precisely and efficiently combat cardiovascular disease is therefore deemed more essential than ever. RNA editing, the cell-intrinsic deamination of adenosine or cytidine RNA residues, changes the molecular identity of edited nucleotides, severely altering the fate of RNA molecules involved in key biological processes. The most common type of RNA editing is the deamination of adenosine residue to inosine (A-to-I), which is catalysed by adenosine deaminases acting on RNA (ADARs). Recent efforts have convincingly liaised RNA editing-based mechanisms to the pathophysiology of the cardiovascular system. In this review, we will briefly introduce the basic concepts of the RNA editing field of research. We will particularly focus our discussion on the therapeutic exploitation of RNA editing as a novel therapeutic tool as well as the future perspectives for its use in cardiovascular disease treatment.
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Birgaoanu et al. (2022) conducted a review in Cardiovascular disease. Site-directed RNA editing (SDRE) was evaluated. Site-directed RNA editing represents a novel, programmable, and reversible therapeutic approach with significant potential for treating cardiovascular diseases by correcting pathogenic point mutations.
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