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New Opportunities for Kinase Drug Repurposing and Target Discovery

Overview
Journal Br J Cancer
Specialty Oncology
Date 2018 Mar 17
PMID 29545596
Citations 17
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Abstract

Protein kinases are major drug targets for oncology. The large size of the kinome, active site conservation and the influence of activation states on drug binding complicates the analysis of their cellular mode of action. In a recent article in Science, Klaeger et al. analysed cellular targets of 243 drug candidates providing a large repository of data for drug repurposing.

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References
1.
Fabian M, Biggs 3rd W, Treiber D, Atteridge C, Azimioara M, Benedetti M . A small molecule-kinase interaction map for clinical kinase inhibitors. Nat Biotechnol. 2005; 23(3):329-36. DOI: 10.1038/nbt1068. View

2.
Yakes F, Chen J, Tan J, Yamaguchi K, Shi Y, Yu P . Cabozantinib (XL184), a novel MET and VEGFR2 inhibitor, simultaneously suppresses metastasis, angiogenesis, and tumor growth. Mol Cancer Ther. 2011; 10(12):2298-308. DOI: 10.1158/1535-7163.MCT-11-0264. View

3.
Fabbro D, Cowan-Jacob S, Moebitz H . Ten things you should know about protein kinases: IUPHAR Review 14. Br J Pharmacol. 2015; 172(11):2675-700. PMC: 4439867. DOI: 10.1111/bph.13096. View

4.
Ciceri P, Muller S, OMahony A, Fedorov O, Filippakopoulos P, Hunt J . Dual kinase-bromodomain inhibitors for rationally designed polypharmacology. Nat Chem Biol. 2014; 10(4):305-12. PMC: 3998711. DOI: 10.1038/nchembio.1471. View

5.
Vasta J, Corona C, Wilkinson J, Zimprich C, Hartnett J, Ingold M . Quantitative, Wide-Spectrum Kinase Profiling in Live Cells for Assessing the Effect of Cellular ATP on Target Engagement. Cell Chem Biol. 2017; 25(2):206-214.e11. PMC: 5814754. DOI: 10.1016/j.chembiol.2017.10.010. View