Cells were seeded (1 × 103 cells/well) in 96-well plates for 24 hours. The next day, indicated concentrations of FGFR inhibitors were added to fresh medium and the cells were incubated for 5 days. After 5 days, cell viability was assessed using a CellTiter 96 AQueous Non-Radioactive Cell Proliferation kit (Promega; Madison, WI) according to manufacturer’s instructions. Briefly, MTS reagent was added to the cells for 2 hours, then absorbance at 490 nm was measured using a SynergyMx microplate reader (BioTek; Winooski, VT). The viable cells are expressed as the cell viability fraction of FGFR inhibitor-treated cells as compared to the untreated control cells.
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