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. 2014 Oct 13;28(1):117–119. doi: 10.1111/pcmr.12316

Table 1.

Sensitivity of the 25 melanoma cell lines to trametinib and their mutation status

Cell line ID NRAS BRAF NF1 PROTEIN TRAMETINIB ICI50 (nM)
C058 WT L597P NA 0.15
M14 WT V600E NA 0.6
C32 WT V600E NA 0.7
HT144 WT V600E NA 1
MR1010B WT V600E NA 2.5
A101D WT V600E NA 3
IGR1 WT V600E NA 4
ISTMEL1 WT V600E NA >10
C089 WT V600E POSITIVE 0.2
D35 WT WT POSITIVE 0.4
A04 WT WT POSITIVE 0.4
C052 WT WT POSITIVE 0.5
C037 WT Translocation POSITIVE 0.5
D10 WT WT POSITIVE 0.6
D38 WT WT POSITIVE 1.3
CHL-1 WT WT POSITIVE 9
Colo-792 WT WT NEGATIVE 0.4
C008 WT WT NEGATIVE 0.6
C067 WT WT NEGATIVE 0.7
C025 WT WT NEGATIVE 0.9
MeWo WT WT NEGATIVE 1
C086 WT WT NEGATIVE 1.3
C077 WT WT NEGATIVE 5
C021 WT WT NEGATIVE 8
D24 WT WT NEGATIVE 10

Each cell lines was treated with nine different concentrations of trametinib (range 0.08–10 nM) for 6 days, fixed and stained with Syto60. The relative viability was calculated versus the vehicle treated control. The IC50 was calculated from the dose response curve. Experiments were performed in triplicate. The mutation status was assessed by Sequenom MassArray platform. NF1 protein expression was evaluated by Western blotting, as described in Figure1. NA = not analysed. C037 cell line carries a BRAF translocation (see Data S1). See also Table S1.