| Literature DB >> 35128925 |
Hiromasa Yoshioka1, Tatsuro Kawamura2, Makoto Muroi1,2, Yasumitsu Kondoh1, Kaori Honda1, Makoto Kawatani1, Harumi Aono1, Herbert Waldmann3, Nobumoto Watanabe2, Hiroyuki Osada1,2.
Abstract
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.Entities:
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Year: 2022 PMID: 35128925 DOI: 10.1021/acschembio.2c00028
Source DB: PubMed Journal: ACS Chem Biol ISSN: 1554-8929 Impact factor: 5.100