The endoplasmic reticulum participated in drug metabolic toxicity

Cell Biol Toxicol. 2022 Dec;38(6):945-961. doi: 10.1007/s10565-021-09689-8. Epub 2022 Jan 18.

Abstract

Covalent binding of reactive metabolites formed by drug metabolic activation with biological macromolecules is considered to be an important mechanism of drug metabolic toxicity. Recent studies indicate that the endoplasmic reticulum (ER) could play an important role in drug toxicity by participating in the metabolic activation of drugs and could be a primarily attacked target by reactive metabolites. In this article, we summarize the generation and mechanism of reactive metabolites in ER stress and their associated cell death and inflammatory cascade, as well as the systematic modulation of unfolded protein response (UPR)-mediated adaptive pathways.

Keywords: Apoptosis; Drug metabolic toxicity; Endoplasmic reticulum; Inflammation; Reactive metabolites; Unfolded protein response.

Publication types

  • Review
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Apoptosis*
  • Drug-Related Side Effects and Adverse Reactions* / metabolism
  • Endoplasmic Reticulum / metabolism
  • Endoplasmic Reticulum Stress
  • Humans
  • Unfolded Protein Response