PulseExploreJournal ClubDebatesTrendingResearchersJournals
Instagram
HomeExploreJournal ClubTrending
Synapse
⌘+K
Synapse
April 3, 2026BIOPHYSICS0 citations

Oxidized Disulfiram Derivatives Activate an Integrated Stress Response and Cause Paraptosis of Human Cancer Cells BT474

View Full Paper
MSM. E. SolovievaIOI. V. OdinokovaYSYu. V. Shatalin

Key Points

  • The research aims to explore the effects of oxidized disulfiram derivatives on human cancer cells and their mechanism of inducing cell death.
  • Investigated the effects of oxidized disulfiram metabolites on BT474 human tumor cells.
  • Used aerobic oxidation of diethyldithiocarbamate in the presence of cobalamin.
  • Monitored induced stress in the endoplasmic reticulum and subsequent cell death.
  • The oxidized disulfiram derivatives activated an integrated stress response in BT474 cells.
  • Cell death occurred through paraptosis, a non-apoptotic cell death mechanism.
  • Findings support potential applications of disulfiram and its derivatives in oncology.

Abstract

Disulfiram, a well-known anti-alcohol drug with minimal side effects, as well as other dithiocarbamates are being investigated as part of the “Drug repurposing” program in order to expand their use, including in oncology. In this work, using the example of human tumor cells BT474, it was found that the action of oxidized disulfiram metabolites generated by aerobic oxidation of diethyldithiocarbamate in the presence of the catalyst cobalamin (vitamin B12b) causes stress in the endoplasmic reticulum, and the integrated response to stress leads to cell death through paraptosis. The ability of substances of this class to cause non-apoptotic types of cell death is of interest for the development of new approaches in oncotherapy.

Ask AI
Helpful
Bookmark
Share
View Full Paper

Cite This Study

Solovieva et al. (2025) studied this question.

synapsesocial.com/papers/69cf5d1f5a333a821460abfahttps://doi.org/10.1134/s0006350925700964
Ask AI
Helpful
Bookmark
Share
View Full Paper