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- W2035805526 endingPage "208" @default.
- W2035805526 startingPage "153" @default.
- W2035805526 abstract "because of their important roles in disease and excellent 'druggability', kinases have become the second largest drug target family. The great success of the BCR-ABL inhibitor imatinib in treating chronic myelogenous leukemia illustrates the high potential of kinase inhibitor (KI) therapeutics, but also unveils a major limitation: the development of drug resistance. This is a significant concern as KIs reach large patient populations for an expanding array of indications.we provide an up-to-date understanding of the mechanisms through which KIs function and through which cells can become KI-resistant. We review current and future approaches to overcome KI resistance, focusing on currently approved KIs and KIs in clinical trials. We then discuss approaches to improve KI efficacy and overcome drug resistance and novel approaches to develop less drug resistance-prone KI therapeutics.although drug resistance is a concern for current KI therapeutics, recent progress in our understanding of the underlying mechanisms and promising technological advances may overcome this limitation and provide powerful new therapeutics." @default.
- W2035805526 created "2016-06-24" @default.
- W2035805526 creator A5068771985 @default.
- W2035805526 creator A5082196069 @default.
- W2035805526 date "2011-01-16" @default.
- W2035805526 modified "2023-10-14" @default.
- W2035805526 title "Mechanisms of drug resistance in kinases" @default.
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