Year: 2026
Type: article
Abstract: In two recent studies published in Nature , Wu et al. and Palma et al. elegantly demonstrated that the endogenous ferroptosis suppressor AIF family member 2 (AIFM2, best known as FSP1) is a pharmacologically actionable vulnerability in lung carcinoma and metastatic melanoma. 1 , 2 These findings formally validate the notion that activating ferroptosis might constitute a viable strategy to control developing tumors (which often exhibit defects in apoptotic signaling), 3 potentially paving the way to the development of clinically viable ferroptosis inducers for cancer therapy.
Institutions: Fox Chase Cancer Center, Temple University
Language: English
Subfield: Pulmonary and Respiratory Medicine
Field: Medicine
Domain: Health Sciences
Open Access status: gold
Estimated APC paid: $3,790
OpenAlex ID: W7118071629
