Autophagy in cardiovascular diseases: role of noncoding RNAs

Jinning Gao1, Xiatian Chen1, Chan Shan1

  • 1Institute for Translational Medicine, The Affiliated Hospital of Qingdao University, College of Medicine, Qingdao University, Qingdao 266021, China.

Insights

Noncoding RNAs (ncRNAs) regulate cardiomyocyte autophagy, a process with a dual role in cardiovascular diseases (CVDs). Understanding ncRNA-mediated autophagy is key to developing novel therapies for CVDs.

Area of Science:

  • Molecular Biology
  • Cardiology
  • Genetics

Background:

  • Cardiovascular diseases (CVDs) are the leading global cause of mortality.
  • Cardiomyocyte autophagy is crucial for heart function but has a dual role in CVD pathology.
  • Noncoding RNAs (ncRNAs) are emerging as critical regulators of cellular processes, including autophagy.

Purpose of the Study:

  • To review the regulatory roles of ncRNAs in autophagy within the context of cardiovascular diseases.
  • To elucidate the dual role of autophagy in CVDs and its modulation by ncRNAs.
  • To provide a theoretical basis for developing ncRNAs as therapeutic targets for CVDs.

Main Methods:

  • Literature review summarizing existing research on ncRNAs and autophagy in CVDs.
  • Analysis of the regulatory mechanisms of microRNAs (miRNAs), long ncRNAs (lncRNAs), and circular RNAs (circRNAs) in cardiac autophagy.
  • Synthesis of information on the physiological and pathological roles of ncRNA-modulated autophagy.

Main Results:

  • ncRNAs, including miRNAs, lncRNAs, and circRNAs, significantly regulate cardiomyocyte autophagy.
  • Both excessive and insufficient autophagy, influenced by ncRNAs, can contribute to CVD progression.
  • ncRNAs play complex roles in maintaining cardiac homeostasis or exacerbating disease.

Conclusions:

  • ncRNA-regulated autophagy presents a promising area for understanding CVD etiology and pathogenesis.
  • Targeting ncRNAs involved in autophagy could lead to novel therapeutic strategies for cardiovascular diseases.
  • Further research into ncRNA-autophagy interactions is essential for advancing CVD treatment.

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