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From in vitro to in vivo: intracellular determination of imatinib and nilotinib may be related with clinical outcome
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Open AccessApoptosis and autophagy have opposite roles on imatinib-induced K562 leukemia cell senescence
Imatinib, the anti-Abl tyrosine kinase inhibitor used as first-line therapy in chronic myeloid leukemia (CML), eliminates CML cells mainly by apoptosis and induces autophagy. Analysis of imatinib-treated K562 ...
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Article
Overexpression of the heat-shock protein 70 is associated to imatinib resistance in chronic myeloid leukemia
Imatinib is an effective therapy for chronic myeloid leukemia (CML), a myeloproliferative disorder characterized by the expression of the recombinant oncoprotein Bcr-Abl. In this investigation, we studied an i...
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Article
An amino-acid switch in the BCR-ABL kinase domain modifies sensitivity to imatinib mesylate
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Drug responses of imatinib mesylate-resistant cells: synergism of imatinib with other chemotherapeutic drugs
Imatinib mesylate (STI571, Glivec, Gleevec) is a powerful inhibitor of the tyrosine kinase activity of Bcr-Abl, the oncoprotein responsible for chronic myeloid leukemia (CML). The drug shows great efficacy in ...
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Article
Resistance to daunorubicin-induced apoptosis is not completely reversed in CML blast cells by STI571
The leukemogenic property of BCR-ABL in chronic myeloid leukemia (CML) is critically dependent on its protein tyrosine kinase activity. STI571 inhibits the BCR-ABL kinase activity, the growth and the viability...