Secreted Apoe rewires melanoma cell state vulnerability to ferroptosis.

Abstract

A major therapeutic barrier in melanoma is the coexistence of diverse cellular states marked by distinct metabolic traits. Transitioning from a proliferative to an invasive melanoma phenotype is coupled with increased ferroptosis vulnerability. However, the regulatory circuits controlling ferroptosis susceptibility across melanoma cell states are unknown. In this work, we identified Apolipoprotein E (<i>APOE</i>) as the top lipid-metabolism gene segregating the melanoma MITF^high/AXL^low proliferative/ferroptosis-resistant from MITF^low/AXL^high invasive/ferroptosis-sensitive state. Mechanistically, ApoE secreted by the MITF^high/AXL^low cells protects the invasive phenotype from ferroptosis-inducing agents by reducing the content of peroxidation-prone polyunsaturated fatty acids and boosting GPX4 levels both in vitro and in vivo. Whole-exome sequencing indicates that <i>APOE</i>^high expression in patients with melanoma is associated with resistance to ferroptosis, regardless of <i>APOE</i> germline status. In aggregate, we found a ferroptosis-resistance mechanism between melanoma cell states relying on secreted ApoE and <i>APOE</i>^high expression as a potential biomarker for poor ferroptosis response in melanoma.