2016/03/16 by Harshnira Hitesh Patani, Tom D. Bunney, Nethaji Thiyagarajan +14 · 1 citation
Biochemistry, Genetics and Molecular Biology · #Fibroblast Growth Factor Research #Kruppel-like factors research #Epigenetics and DNA Methylation
paper · pdf · doi:10.18632/oncotarget.8132
openalex publication_date 2016/03/16 · openalex created_date 2025/10/10 · openalex updated_date 2026/07/31
// Harshnira Patani 1, * , Tom D. Bunney 1, * , Nethaji Thiyagarajan 1 , Richard A. Norman 2 , Derek Ogg 2 , Jason Breed 2 , Paul Ashford 1 , Andrew Potterton 1 , Mina Edwards 1 , Sarah V. Williams 3 , Gary S. Thomson 4 , Camilla S.M. Pang 1 , Margaret A. Knowles 3 , Alexander L. Breeze 4 , Christine Orengo 1 , Chris Phillips 2 , Matilda Katan 1 1 Institute of Structural and Molecular Biology, Division of Biosciences, University College London, Gower St, London WC1E 6BT, UK 2 Discovery Sciences, AstraZeneca, Mereside, Alderley Park, Macclesfield, Cheshire SK10 4TG, UK 3 Section of Experimental Oncology, Leeds Institute of Molecular Medicine, St James’s University Hospital, Leeds LS9 7TF, UK 4 Astbury Centre for Structural Molecular Biology, Faculty of Biological Sciences, University of Leeds, Leeds LS2 9JT, UK * These authors have contributed equally to this work Correspondence to: Tom D. Bunney, e-mail: [email protected] Matilda Katan, e-mail: [email protected] Keywords: precision medicine, cancer mutations, receptor tyrosine kinases, small molecule inhibitors, resistance Received: December 15, 2015     Accepted: February 28, 2016     Published: March 16, 2016 ABSTRACT Frequent genetic alterations discovered in FGFRs and evidence implicating some as drivers in diverse tumors has been accompanied by rapid progress in targeting FGFRs for anticancer treatments. Wider assessment of the impact of genetic changes on the activation state and drug responses is needed to better link the genomic data and treatment options. We here apply a direct comparative and comprehensive analysis of FGFR3 kinase domain variants representing the diversity of point-mutations reported in this domain. We reinforce the importance of N540K and K650E and establish that not all highly activating mutations (for example R669G) occur at high-frequency and conversely, that some “hotspots” may not be linked to activation. Further structural characterization consolidates a mechanistic view of FGFR kinase activation and extends insights into drug binding. Importantly, using several inhibitors of particular clinical interest (AZD4547, BGJ-398, TKI258, JNJ42756493 and AP24534), we find that some activating mutations (including different replacements of the same residue) result in distinct changes in their efficacy. Considering that there is no approved inhibitor for anticancer treatments based on FGFR-targeting, this information will be immediately translatable to ongoing clinical trials.