Why the study?
Understanding of the molecular determinants operating during cardiac aging and repair remains limited.
Key points are not available for this paper at this time.
Design
Review
Long non-coding RNAs represent promising, albeit challenging, novel targets for promoting cardiac regeneration and reprogramming fibroblasts into cardiomyocytes.
Aging imposes a barrier for tissue regeneration. In the heart, aging leads to a severe rearrangement of the cardiac structure and function and to a subsequent increased risk of heart failure. An intricate network of distinct pathways contributes to age-related alterations during healthy heart aging and account for a higher susceptibility of heart disease. Our understanding of the systemic aging process has already led to the design of anti-aging strategies or to the adoption of protective interventions. Nevertheless, our understanding of the molecular determinants operating during cardiac aging or repair remains limited. Here, we will summarize the molecular and physiological alterations that occur during aging of the heart, highlighting the potential role for long non-coding RNAs (lncRNAs) as novel and valuable targets in cardiac regeneration/repair.
No takes yet. Share an insight, caveat, or question.
Santos et al. (2021) studied this question.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: