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In mouse models, the team introduced combined therapy including PD-L1 blocker and cyst(e) inase (a bioengineered enzyme that degrades cystine and cysteine) and such treatment can enhance the efficacy of CTL-mediated anticancer effects, supporting the idea that inducing ferroptosis could be considered a productive way for treating cancer and overcoming immunotherapy resistance (Wang et al., 2019)

While specific pro-oxidant initiators have not yet been identified, candidates with low oxidation potentials include metals, either derived from device coils or leftover from the manufacturing process, and Furaneol, 4-hydroxy-2,5-dimethyl-furan-3-on, known as strawberry or pineapple furanone, which has a low oxidation potential and has been implicated in the initiation of some cellular metal-dependent radical processes

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p53 can downregulate the expression of the Xc system component SLC7A11, inhibiting cystine intake and inducing ferroptosis [61]

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