Figure 2.
Figure 2. PD166326 is a more potent inhibitor of Bcr/Abl- and stem cell factor–dependent proliferation than imatinib mesylate. (A) The P210-expressing MO7e cell line R10(-) growing in the absence of exogenous cytokine, and (B) parental MO7e cells growing in the presence of stem cell factor (MO7e/KL) were treated with the indicated concentrations of PD166326 (•) and imatinib mesylate (▴) for 48 hours and then analyzed by [3H]thymidine incorporation as described in “Materials and methods.” Results are expressed as the counts per minute (CPM) relative to cells treated with diluent alone (DMSO) versus the concentration (log10 scale) of PD166326 or imatinib mesylate. The calculated IC50 for each drug is shown. The results depicted are representative of multiple independent experiments.

PD166326 is a more potent inhibitor of Bcr/Abl- and stem cell factor–dependent proliferation than imatinib mesylate. (A) The P210-expressing MO7e cell line R10(-) growing in the absence of exogenous cytokine, and (B) parental MO7e cells growing in the presence of stem cell factor (MO7e/KL) were treated with the indicated concentrations of PD166326 (•) and imatinib mesylate (▴) for 48 hours and then analyzed by [3H]thymidine incorporation as described in “Materials and methods.” Results are expressed as the counts per minute (CPM) relative to cells treated with diluent alone (DMSO) versus the concentration (log10 scale) of PD166326 or imatinib mesylate. The calculated IC50 for each drug is shown. The results depicted are representative of multiple independent experiments.

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