Apoptosis in chronic myeloid leukemia cells transiently treated with imatinib or dasatinib is caused by residual BCR-ABL kinase inhibition.

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ŠIMARA Pavel STEJSKAL Stanislav KRONTORÁD KOUTNÁ Irena POTĚŠIL David TESAŘOVÁ Lenka POTĚŠILOVÁ Michaela ZDRÁHAL Zbyněk MAYER Jiří

Rok publikování 2013
Druh Článek v odborném periodiku
Časopis / Zdroj American Journal of Hematology
Fakulta / Pracoviště MU

Fakulta informatiky

Citace
www PubMed
Doi http://dx.doi.org/10.1002/ajh.23419
Obor Onkologie a hematologie
Klíčová slova Chronic Myeloid Leukemia; Imatinib; Dasatinib
Přiložené soubory
Popis Transient, potent BCR-ABL inhibition with tyrosine kinase inhibitors (TKIs) was recently demonstrated to be sufficient to commit chronic myeloid leukemia (CML) cells to apoptosis irreversibly. This mechanism explains the clinical efficacy of once-daily dasatinib treatment, despite the rapid clearance of the drug from the plasma. However, our in vitro data suggest that apoptosis induction after transient TKI treatment, observed in the BCR-ABL-positive cell lines K562, KYO-1, and LAMA-84 and progenitor cells from chronic phase CML patients, is instead caused by a residual kinase inhibition that persists in the cells as a consequence of intracellular drug retention. High intracellular concentrations of imatinib and dasatinib residues were measured in transiently treated cells. Furthermore, the apoptosis induced by residual imatinib or dasatinib from transient treatment could be rescued by washing out the intracellularly retained drugs. The residual kinase inhibition was also undetectable by the phospho-CRKL assay. These findings confirm that continuous target inhibition is required for the optimal efficacy of kinase inhibitors.
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