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. 2018 Oct 15;26(8):1365–1378. doi: 10.1038/s41418-018-0210-8

Fig. 6.

Fig. 6

Accurate prediction of cell line sensitisation to trametinib by pharmacological inhibitors. a, b SK-MEL147 cells were pre-treated with JNK inhibitor V (5 µM); c, d MEL-JUSO cells were pre-treated with Defactinib (5 µM); e, f WM1205-LU cells were pre-treated with either inhibitor or a combination of both. Subsequently, cells were treated with trametinib (10 nM) and phosphorylation of key kinases, as well as cell viability were determined (48 h) using multiplex ELISA and resazurin reduction assay, respectively. Data show averaged median fluorescence intensity (MFI) for each protein (means ± S.D. from n = 3 independent experiments) and or cell viability relative to control values of 100% (means + S.E.M. from n = 3 independent experiments). Statistical analysis was performed using two-way ANOVA with post-hoc Tukey test