Exponentially growing KCL22, LAMA-84, and K562 cells from routine cultures were seeded in fresh medium at 3 × 105 cells/mL. Cells were treated with dimethyl-sulfoxide (DMSO; vehicle) or increasing doses of TKi at the beginning of incubation (treatment at time 0). Half maximal inhibitory concentration (IC50) values were determined by counting viable cells following trypan blue staining after 72 h of treatment and processing data with GraphPad Prism software (La Jolla, CA, USA).
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