When exposed to 0.1 μM of the TKI, the intracellular imatinib concentration in P-gp overexpressing cells was significantly reduced ( p = 0.0138), whereas intracellular reductions of asciminib, dasatinib and bosutinib of 16.7%, 9.6% and 9.7%, respectively, did not reach statistical significance.
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Characterizing P-glycoprotein and Breast Cancer Resistance Protein interactions of asciminib among other tyrosine kinase inhibitors used in chronic myeloid leukemia.
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