a, HRASV12-expressing cell lines are sensitive to erastin, whereas isogenic lines lacking HRASV12 are resistant, as determined by Trypan blue exclusion; the graph is a representative outcome of multiple independent experiments. b, Transmission electron microscopy images (×20,000) of BJ-TERT/LT/ST/RASV12 mitochondria after cells were treated with nothing, erastin (37 μM for 10 h) or staurosporine (STS, 1 μM for 5 h). c, Phase-contrast photograph of BJ-TERT/LT/ST/RASV12 cells 24 h after 9 μM erastin treatment indicates that nuclei are intact after cell death. d, Anti-oxidants suppress erastin-induced death in BJ-TERT/LT/ST/RASV12 cells. BHT, butylated hydroxytoluene; DMSO, dimethylsulphoxide. e, Level of intracellular oxidative species in BJ-TERT/LT/ST/RASV12 (black line) or BJ-TERT (grey line) cells treated with 4.6 μM erastin. y axis, percentage of cells exhibiting dichlorofluorescein (DCF) fluorescence within region of interest, M1, as measured by flow cytometry; error bars, one standard deviation, n = 2. f, PARP1 cleavage is not seen during erastin-induced cell death in A-673, HT-1080 and HeLa cells. NT, no treatment. g, STS, but not erastin, induces cytochrome c (cyt c) release from BJ-TERT/LT/ST/RASV12 mitochondria; mitochondrial fraction, mito; cytosolic fraction, cyto. h, Pro-caspase-3 is not cleaved in response to erastin.