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biorxiv.org/content/10.648 Using a suite of robust genetic and pharmacological methods, we failed to impact the growth of established tumors upon inhibition of GPX4, GCLC, or SLC7A11, despite robust activation of ferroptosis in these models in vitro.We therefore expanded our analysis to 100 cell lines and identified heterogeneous responses to canonical ferroptosis induces and suppressors which could be organized into biologically distinct response classes.Among these, we identified two classes of cell lines that are very sensitive to GCLC inhibitor BSO, triggering either ferroptotic or non-ferroptotic cell death