In this article, we are reviewing the molecular mechanisms that lead to kinase inhibitor resistance. As the oncogenic BCR-ABL kinase is the target of the first approved small-molecule kinase inhibitor imatinib, we will first focus on the structural and mechanistic basis for imatinib resistance. We will then show ways how next generations of BCR-ABL inhibitors and alternative targeting strategies have helped to offer effective treatment options for imatinib-resistant patients. Based on these insights, we discuss commonalities and further mechanisms that lead to resistance to other kinase inhibitors in solid tumors. This article is part of a Special Issue entitled: Inhibitors of Protein Kinases (2012). (C) 2012 Elsevier B.V. All rights reserv...
The leukemogenic tyrosine kinase Bcr-AbI contains a highly conserved inhibitor-binding pocket (IBP),...
Abstract Bcr-Abl inhibitors paved the way of targeted therapy epoch. Imatinib was the first tyrosine...
The deregulated activity of BCR-ABL tyrosine kinase originating from the t(9;22) chromosomal translo...
Resistance to imatinib is commonly associated with reactivation of BCR-ABL signaling. Many such pati...
Since the introduction of imatinib mesylate for the treatment of chronic myeloid leukaemia, impressi...
Imatinib (Gleevec/STI-571/CGP57148B, Novartis) is a small-molecule, tyrosine kinase inhibitor develo...
Since the introduction of imatinib mesylate (IM) for the treatment of chronic myeloid leukemia (CML)...
The discovery of tyrosine kinases that, once deregulated, can cause malignancy, allowed the developm...
Cancer is the leading causes of human deaths all over the world. The growing understanding in cancer...
AbstractThe ABL inhibitor imatinib is a highly effective therapy for patients with chronic myeloid l...
BCR-ABL is the oncogenic protein-tyrosine kinase responsible for the pathogenesis of chronic myeloge...
Resistance to the BCR-ABL inhibitor imatinib mesylate (IM) poses a major problem for the treatment o...
The efficacy of imatinib in chronic myeloid leukemia has been remarkable, but the development of res...
AbstractThe fusion tyrosine kinase Bcr-Abl plays a fundamental role in the pathogenesis of chronic m...
The emergence of resistance to imatinib has become a significant problem despite the remarkable clin...
The leukemogenic tyrosine kinase Bcr-AbI contains a highly conserved inhibitor-binding pocket (IBP),...
Abstract Bcr-Abl inhibitors paved the way of targeted therapy epoch. Imatinib was the first tyrosine...
The deregulated activity of BCR-ABL tyrosine kinase originating from the t(9;22) chromosomal translo...
Resistance to imatinib is commonly associated with reactivation of BCR-ABL signaling. Many such pati...
Since the introduction of imatinib mesylate for the treatment of chronic myeloid leukaemia, impressi...
Imatinib (Gleevec/STI-571/CGP57148B, Novartis) is a small-molecule, tyrosine kinase inhibitor develo...
Since the introduction of imatinib mesylate (IM) for the treatment of chronic myeloid leukemia (CML)...
The discovery of tyrosine kinases that, once deregulated, can cause malignancy, allowed the developm...
Cancer is the leading causes of human deaths all over the world. The growing understanding in cancer...
AbstractThe ABL inhibitor imatinib is a highly effective therapy for patients with chronic myeloid l...
BCR-ABL is the oncogenic protein-tyrosine kinase responsible for the pathogenesis of chronic myeloge...
Resistance to the BCR-ABL inhibitor imatinib mesylate (IM) poses a major problem for the treatment o...
The efficacy of imatinib in chronic myeloid leukemia has been remarkable, but the development of res...
AbstractThe fusion tyrosine kinase Bcr-Abl plays a fundamental role in the pathogenesis of chronic m...
The emergence of resistance to imatinib has become a significant problem despite the remarkable clin...
The leukemogenic tyrosine kinase Bcr-AbI contains a highly conserved inhibitor-binding pocket (IBP),...
Abstract Bcr-Abl inhibitors paved the way of targeted therapy epoch. Imatinib was the first tyrosine...
The deregulated activity of BCR-ABL tyrosine kinase originating from the t(9;22) chromosomal translo...