Understanding the Protective Role of Exosomes in Doxorubicin-Induced Cardiotoxicity

Oxid Med Cell Longev. 2022 Sep 12:2022:2852251. doi: 10.1155/2022/2852251. eCollection 2022.

Abstract

Doxorubicin (DOX) is a class of effective chemotherapeutic agents widely used in clinical practice. However, its use has been limited by cardiotoxicity. The mechanism of DOX-induced cardiotoxicity (DIC) is complex, involving oxidative stress, Ca2+ overload, inflammation, pyroptosis, ferroptosis, apoptosis, senescence, etc. Exosomes (EXOs), as extracellular vesicles (EVs), play an important role in the material exchange and signal transmission between cells by carrying components such as proteins and RNAs. More recently, there has been a growing number of publications focusing on the protective effect of EXOs on DIC. Here, this review summarized the main mechanisms of DIC, discussed the mechanism of EXOs in the treatment of DIC, and further explored the value of EXOs as diagnostic biomarkers and therapeutic strategies for DIC.

Publication types

  • Review

MeSH terms

  • Apoptosis
  • Biomarkers / metabolism
  • Cardiotoxicity* / drug therapy
  • Cardiotoxicity* / etiology
  • Cardiotoxicity* / prevention & control
  • Doxorubicin / adverse effects
  • Exosomes* / metabolism
  • Humans
  • Myocytes, Cardiac / metabolism
  • Oxidative Stress

Substances

  • Biomarkers
  • Doxorubicin