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Identification of a Small Molecule That Enhances Ferroptosis via Inhibition of Ferroptosis Suppressor Protein 1 (FSP1).

Hiromasa YoshiokaTatsuro KawamuraMakoto MuroiYasumitsu KondohKaori HondaMakoto KawataniHarumi AonoHerbert WaldmannNobumoto WatanabeHiroyuki Osada
Published in: ACS chemical biology (2022)
Glutathione peroxidase 4 (GPX4) is an intracellular enzyme that oxidizes glutathione while reducing lipid peroxides and is a promising target for cancer therapy. To date, several GPX4 inhibitors have been reported to exhibit cytotoxicity against cancer cells. However, some cancer cells are less sensitive to the known GPX4 inhibitors. This study aimed to explore compounds showing synergistic effects with GPX4 inhibitors. We screened a chemical library and identified a compound named NPD4928, whose cytotoxicity was enhanced in the presence of a GPX4 inhibitor. Furthermore, we identified ferroptosis suppressor protein 1 as its target protein. The results indicate that NPD4928 enhanced the sensitivity of various cancer cells to GPX4 inhibitors, suggesting that the combination might have therapeutic potential via the induction of ferroptosis.
Keyphrases
  • cell death
  • small molecule
  • cancer therapy
  • protein protein
  • amino acid
  • drug delivery
  • binding protein
  • nitric oxide