Recent Advances in Modulating Mitophagy with Novel Drugs/Compounds

A special issue of Pharmaceuticals (ISSN 1424-8247). This special issue belongs to the section "Pharmacology".

Deadline for manuscript submissions: 5 February 2025 | Viewed by 67

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Guest Editor
Genetics and Genome Sciences, University of Connecticut Health Center, Farmington, CT, USA
Interests: innate immunity; molecular and cell biology; stem cell technology
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Dear Colleagues,

Heart disease is a major threat to human health. Every day, 2396 people die from cardiovascular disease, according to 2019 data (obtained from The American Heart Association). Mitochondria are the most important organelles that provide cellular energy by liberating chemical energy via oxidative phosphorylation and then converting this energy in the form of ATP. The heart is beating all the time, and the demand for energy is very high, so mitochondrial damage can cause serious heart disease. Mitochondria are in a dynamic balance of continuous division and fusion. Damaged mitochondria are engulfed by lysosomes and degraded; this process was named mitophagy. Mitophagy provides an important guarantee for mitochondrial quality control. Thus, looking for solutions to heart disease from the perspective of mitophagy will be an important direction of future research for cardiomyopathy, including (but not limited to) searching for novel drugs or compounds that modulate the mitophagy process, exploring how drugs treat heart disease by affecting the mitophagy mechanism, and investigating how drug delivery can improve the treatment of heart disease.

This Special Issue on “Recent Advances in Modulating Mitophagy with Novel Drugs/Compounds” aims to provide up-to-date insights into the remarkable complexity of mitophagy and on its dysregulation in the context of many different kinds of heart diseases. We look forward to receiving your contributions.

Dr. Mingchong Yang
Guest Editor

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Keywords

  • heart disease
  • mitochondria
  • mitophagy
  • mitochondrial quality control
  • drug screening

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