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. 2021 Feb 8;29(4):434–444. doi: 10.4062/biomolther.2020.203

Fig. 1.

Fig. 1

Effects of PLX4720 on cell growth and autophagy in cells with different BRAF mutational status. (A) Whole-cell lysates were immunoblotted with antibodies against phospho-ERK, ERK, phospho-MEK and MEK. Cells were BRAF homozygous or heterozygous for wild-type (WT), or V600E (E) mutation. (B) Cell viability, measured through WST-1 assay, relative to vehicle controls in four cell lines exposed to PLX4720 (0.1-10 μM) for 72 h. Values represent the mean ± SD of quadruplicate determinants from one of three representative experiments.