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Ferroptosis is mediated by multiple mechanisms including lipid peroxidation, iron overload and dysfunction of the antioxidant system (Fig

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These include cAMP response element (CRE)-based reporter genes for G alpha i/o, G alpha s-coupled GPCRs, Nuclear Factor Activator of Transcription (NFAT)-based reporters for G alpha q/11 or the promiscuous Gprotein G alpha15/16-coupled receptors and MAP kinase reporter genes for use in Galpha i/o coupled receptors (Selbie & Hill, 1998