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. Author manuscript; available in PMC: 2017 Nov 1.
Published in final edited form as: Clin Cancer Res. 2016 May 23;22(21):5312–5321. doi: 10.1158/1078-0432.CCR-15-1101

Figure 3. In Vitro Response to Co-inhibition of MAPK and mTOR pathways in Isogenic Mouse BRAFV600E and BRAFWT Cells.

Figure 3

Assessments of isogenic murine (A–B) BRAFV600E and (C–D) BRAFWT cells in response to treatment with AZD6244 + everolimus, everolimus + PLX4720 or AZD6244 + PLX4720. (A, C) Represent cell viability data assessed 72 hours after treatment. Means of six replicates with standard errors are displayed. Measurements are normalized to DMSO controls. (B, D) Western blot analyses of p-Akt, p-ERK and p-S6 in isogenic murine (B) BRAFV600E and (D) BRAFWT cells. β-actin was used as loading control. Levels of p-Akt, p-ERK and p-S6 were determined 1 and 6 hours after treatment. For all of the above results, in samples receiving combination therapy, inhibitors were administered simultaneously.