Figure 5
Figure 5. Effect of three tyrosine kinase inhibitors on the proliferation of the 2 ROSA cell lines. Cells were cultured for 48 hours in the presence of imatinib, dasatinib or midostaurin (1 μM, provided in dimethylsulfoxide (DMSO) 0.1% final concentration) or in the presence of DMSO alone (0.1% final concentration) in the established culture medium (containing rhSCF at 80 ng/mL for ROSAKIT WT cells but not for ROSAKIT D816V cells). At the end of this incubation, 10 μL of MTT was added in each well and the cells were incubated for 3 additional hours at 37°C. The number of living cells was then measured for each condition by reading the absorbance at 570 nm, and the results were expressed as a percentage of living cells compared with the control (DMSO 0.1% alone). Data presented are the mean ± SD from 3 independent experiments. ***Significantly different from control (DMSO alone) at P < .0001.

Effect of three tyrosine kinase inhibitors on the proliferation of the 2 ROSA cell lines. Cells were cultured for 48 hours in the presence of imatinib, dasatinib or midostaurin (1 μM, provided in dimethylsulfoxide (DMSO) 0.1% final concentration) or in the presence of DMSO alone (0.1% final concentration) in the established culture medium (containing rhSCF at 80 ng/mL for ROSAKIT WT cells but not for ROSAKIT D816V cells). At the end of this incubation, 10 μL of MTT was added in each well and the cells were incubated for 3 additional hours at 37°C. The number of living cells was then measured for each condition by reading the absorbance at 570 nm, and the results were expressed as a percentage of living cells compared with the control (DMSO 0.1% alone). Data presented are the mean ± SD from 3 independent experiments. ***Significantly different from control (DMSO alone) at P < .0001.

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