Eprenetapopt triggers ferroptosis, inhibits NFS1 cysteine desulfurase, and synergizes with serine and glycine dietary restriction
- Author(s)
- Fujihara, KM; Zhang, BZ; Jackson, TD; Ogunkola, MO; Nijagal, B; Milne, JV; Sallman, DA; Ang, CS; Nikolic, I; Kearney, CJ; Hogg, SJ; Cabalag, CS; Sutton, VR; Watt, S; Fujihara, AT; Trapani, JA; Simpson, KJ; Stojanovski, D; Leimkuhler, S; Haupt, S; Phillips, WA; Clemons, NJ;
- Details
- Publication Year 2022-09-16,Volume 8,Issue #37,Page eabm9427
- Journal Title
- Science Advances
- Publication Type
- Research article
- Abstract
- The mechanism of action of eprenetapopt (APR-246, PRIMA-1(MET)) as an anticancer agent remains unresolved, although the clinical development of eprenetapopt focuses on its reported mechanism of action as a mutant-p53 reactivator. Using unbiased approaches, this study demonstrates that eprenetapopt depletes cellular antioxidant glutathione levels by increasing its turnover, triggering a nonapoptotic, iron-dependent form of cell death known as ferroptosis. Deficiency in genes responsible for supplying cancer cells with the substrates for de novo glutathione synthesis (SLC7A11, SHMT2, and MTHFD1L), as well as the enzymes required to synthesize glutathione (GCLC and GCLM), augments the activity of eprenetapopt. Eprenetapopt also inhibits iron-sulfur cluster biogenesis by limiting the cysteine desulfurase activity of NFS1, which potentiates ferroptosis and may restrict cellular proliferation. The combination of eprenetapopt with dietary serine and glycine restriction synergizes to inhibit esophageal xenograft tumor growth. These findings reframe the canonical view of eprenetapopt from a mutant-p53 reactivator to a ferroptosis inducer.
- Department(s)
- Laboratory Research
- PubMed ID
- 36103522
- Publisher's Version
- https://doi.org/10.1126/sciadv.abm9427
- Open Access at Publisher's Site
- https://doi.org/10.1126/sciadv.abm9427
- Terms of Use/Rights Notice
- Refer to copyright notice on published article.
Creation Date: 2024-10-25 06:46:39
Last Modified: 2024-10-25 06:48:14