Figure 2.
Turnover of the FLT3 receptor. (A) Molm14 and MV411 cells (each harboring a FLT3-ITD mutation) and primary AML samples (2 from patients with FLT3-ITD mutations, 1 from a patient with wild-type FLT3) were cultured in the presence or absence of 50 μg/mL cycloheximide. At designated time points, cells were harvested and analyzed for total FLT3 expression by immunoblotting. Densitometric results were analyzed by regression analysis after linear conversion to estimate a t1/2. (B) Whole blood was collected at designated time points after dosing from a participant receiving 100 mg per day FF-10101 who had circulating blasts at enrollment. For each time point, half of the sample was used to directly isolate and analyze P-FLT3 from the circulating blasts whereas the other half was used to isolate plasma for the PIA assay using Molm14 cells.

Turnover of the FLT3 receptor. (A) Molm14 and MV411 cells (each harboring a FLT3-ITD mutation) and primary AML samples (2 from patients with FLT3-ITD mutations, 1 from a patient with wild-type FLT3) were cultured in the presence or absence of 50 μg/mL cycloheximide. At designated time points, cells were harvested and analyzed for total FLT3 expression by immunoblotting. Densitometric results were analyzed by regression analysis after linear conversion to estimate a t1/2. (B) Whole blood was collected at designated time points after dosing from a participant receiving 100 mg per day FF-10101 who had circulating blasts at enrollment. For each time point, half of the sample was used to directly isolate and analyze P-FLT3 from the circulating blasts whereas the other half was used to isolate plasma for the PIA assay using Molm14 cells.

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