Mechanisms and Drug Intervention for Doxorubicin-Induced Cardiotoxicity Based on Mitochondrial Bioenergetics

Oxid Med Cell Longev. 2022 Oct 14:2022:7176282. doi: 10.1155/2022/7176282. eCollection 2022.

Abstract

Doxorubicin (DOX) is an anthracycline chemotherapy drug, which is indispensable in antitumor therapy. However, its subsequent induction of cardiovascular disease (CVD) has become the primary cause of mortality in cancer survivors. Accumulating evidence has demonstrated that cardiac mitochondrial bioenergetics changes have become a significant marker for doxorubicin-induced cardiotoxicity (DIC). Here, we mainly summarize the related mechanisms of DOX-induced cardiac mitochondrial bioenergetics disorders reported in recent years, including mitochondrial substrate metabolism, the mitochondrial respiratory chain, myocardial ATP storage and utilization, and other mechanisms affecting mitochondrial bioenergetics. In addition, intervention for DOX-induced cardiac mitochondrial bioenergetics disorders using chemical drugs and traditional herbal medicine is also summarized, which will provide a comprehensive process to study and develop more appropriate therapeutic strategies for DIC.

Publication types

  • Review

MeSH terms

  • Adenosine Triphosphate / metabolism
  • Cardiotoxicity* / metabolism
  • Doxorubicin / adverse effects
  • Energy Metabolism
  • Heart Diseases* / chemically induced
  • Heart Diseases* / drug therapy
  • Heart Diseases* / metabolism
  • Humans
  • Myocytes, Cardiac / metabolism

Substances

  • Doxorubicin
  • Adenosine Triphosphate