| Literature DB >> 27070691 |
Daniel M Freed1, Jin H Park1, Ravi Radhakrishnan2, Mark A Lemmon3.
Abstract
Effective clinical application of conformationally selective kinase inhibitors requires tailoring drug choice to the tumor's activating mutation(s). In this issue of Cancer Cell, Foster et al. (2016) describe how activating deletions in BRAF, EGFR, and HER2 cause primary resistance to common inhibitors, suggesting strategies for improved inhibitor selection.Entities:
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Year: 2016 PMID: 27070691 PMCID: PMC5028821 DOI: 10.1016/j.ccell.2016.03.017
Source DB: PubMed Journal: Cancer Cell ISSN: 1535-6108 Impact factor: 31.743