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Targeting autophagy in aortic aneurysm and dissection.

Ze-Min Fang1, Xin Feng1, Yue Chen1

  • 1Division of Cardiothoracic and Vascular Surgery, Sino-Swiss Heart-Lung Transplantation Institute, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, Hubei, China.

Biomedicine & Pharmacotherapy = Biomedecine & Pharmacotherapie
|September 9, 2022
PubMed
Summary

Autophagy, a cellular process, is implicated in aortic aneurysm and dissection (AAD). While its role is debated, targeting autophagy may offer new therapeutic strategies for this serious aortic disease.

Keywords:
Aortic aneurysmAortic dissectionAutophagyMetforminRapamycinSingle-cell RNA sequencing

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Area of Science:

  • Cellular Biology
  • Cardiovascular Medicine
  • Molecular Biology

Background:

  • Autophagy is a fundamental cellular process crucial for maintaining homeostasis.
  • Evidence links autophagy to cardiovascular diseases including aneurysm, aortic dissection, atherosclerosis, and ischemia-reperfusion injury.
  • Aortic aneurysm and dissection (AAD) is a severe condition lacking effective drug treatments.

Purpose of the Study:

  • To review experimental evidence on autophagy's role in aortic aneurysm and dissection (AAD).
  • To discuss the controversial functions of autophagy in AAD pathogenesis.
  • To explore potential therapeutic strategies targeting autophagy for AAD.

Main Methods:

  • Literature review of experimental studies on autophagy in AAD.
  • Analysis of research on autophagy-related genes (e.g., ATG5, ATG7).
  • Examination of studies investigating autophagy activators (e.g., rapamycin, metformin) in AAD models.
  • Inclusion of recent single-cell RNA sequencing research on AAD.

Main Results:

  • Autophagy is activated in AAD, but its precise role remains controversial.
  • Inhibition of autophagy (e.g., via ATG5/ATG7 knockout) can exacerbate AAD.
  • Autophagy activators like rapamycin and metformin show promise in delaying AAD progression.
  • Single-cell RNA sequencing provides new insights into AAD mechanisms.

Conclusions:

  • Targeting autophagy presents a potential novel therapeutic avenue for AAD.
  • Further research is needed to clarify the complex role of autophagy in AAD.
  • Overcoming current research challenges is crucial for advancing AAD treatment.