To identify potential therapies for patients with NRAS mutant tumors, we tested the sensitivity of 6 NRAS mutant NSCLC cell lines (Table S3) against a variety of kinase inhibitors in in vitro cell growth inhibition assays (Fig. 2A). None of the lines were sensitive (with lower than 1 micromolar IC50s) to the EGFR TKI, erlotinib, the ALK/MET/RON/ROS1 inhibitor, crizotinib, or the IGF-1R inhibitor, linsitinib. By contrast, 5 of 6 lines were sensitive to two different MEK inhibitors, selumetinib and trametinib.