Ferroptosis is a novel form of programmed cell death. We found that the ferroptosis sensitivity in renal and ovarian cancers are regulated by cell density through TAZ-EMP1-NOX4 and TAZ-ANGPTL4-NOX2 pathway, respectively. These findings reveal TAZ as a novel genetic determinant of ferroptosis. Triggering ferroptosis may have therapeutic potential for TAZ-activated tumors.
Keywords: Angiopoietin-Like 4 (ANGPTL4); Epithelial Membrane Protein 1 (EMP1); Erastin; Ferroptosis; Hippo pathway; NADPH Oxidase 2 (NOX2); NADPH Oxidase 4 (NOX4); Ovarian Cancer; Renal Cell Carcinoma; Yes-associated protein 1 (YAP1); transcriptional coactivator with PDZ-binding motif (TAZ).
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