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. Author manuscript; available in PMC: 2015 Apr 13.
Published in final edited form as: Melanoma Res. 2014 Jun;24(3):207–218. doi: 10.1097/CMR.0000000000000060

Fig. 2.

Fig. 2

Both BRAF wildtype and mutant melanoma cells are more sensitive to irreversible multi-erbB inhibitors canertinib than single-erbB or dual-erbB targeting agents. Dose-dependent response curves of growth inhibition in BRAF WT (a) and V600E mutant (b) cells by 3-day treatment of gefitinib, lapatinib, erlotinib, and canertinib. Cell viability after each drug treatment was assessed by MTT assay compared with vehicle control treatment and expressed as percent vehicle control (% control). n = 3–4 experiments. WT, wildtype.