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dc.contributor.authorSmyth, EC
dc.contributor.authorBabina, IS
dc.contributor.authorTurner, NC
dc.date.accessioned2017-03-24T15:09:07Z
dc.date.issued2017-03-01
dc.identifier.citationCancer discovery, 2017, 7 (3), pp. 248 - 249
dc.identifier.issn2159-8274
dc.identifier.urihttps://repository.icr.ac.uk/handle/internal/524
dc.identifier.eissn2159-8290
dc.identifier.doi10.1158/2159-8290.cd-17-0057
dc.description.abstract<b/>FGFR2 genetic translocations are frequent in cholangiocarcinoma, yet despite initial sensitivity to FGFR inhibitors in clinic, patients quickly become resistant to targeted therapies. The work published by Goyal and colleagues demonstrates that acquisition of gatekeeper mutations in FGFR2 and intratumoral heterogeneity drive resistance in patients with FGFR2-translocated intrahepatic cholangiocarcinoma, which will have important implications for management of the disease in clinic. Cancer Discov; 7(3); 248-9. ©2017 AACR.See related article by Goyal et al., p. 252.
dc.formatPrint
dc.format.extent248 - 249
dc.languageeng
dc.language.isoeng
dc.publisherAMER ASSOC CANCER RESEARCH
dc.rights.urihttps://creativecommons.org/licenses/by/4.0
dc.subjectBile Ducts, Intrahepatic
dc.subjectHumans
dc.subjectCholangiocarcinoma
dc.subjectBile Duct Neoplasms
dc.subjectLiver Neoplasms
dc.subjectMutation
dc.subjectReceptor, Fibroblast Growth Factor, Type 2
dc.titleGatekeeper Mutations and Intratumoral Heterogeneity in FGFR2-Translocated Cholangiocarcinoma.
dc.typeJournal Article
dcterms.dateAccepted2017-02-01
rioxxterms.versionofrecord10.1158/2159-8290.cd-17-0057
rioxxterms.licenseref.urihttps://creativecommons.org/licenses/by/4.0
rioxxterms.licenseref.startdate2017-03
rioxxterms.typeJournal Article/Review
dc.relation.isPartOfCancer discovery
pubs.issue3
pubs.notesNot known
pubs.organisational-group/ICR
pubs.organisational-group/ICR/Primary Group
pubs.organisational-group/ICR/Primary Group/ICR Divisions
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Breast Cancer Research
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Breast Cancer Research/Molecular Oncology
pubs.organisational-group/ICR/Primary Group/Royal Marsden Clinical Units
pubs.organisational-group/ICR
pubs.organisational-group/ICR/Primary Group
pubs.organisational-group/ICR/Primary Group/ICR Divisions
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Breast Cancer Research
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Breast Cancer Research/Molecular Oncology
pubs.organisational-group/ICR/Primary Group/Royal Marsden Clinical Units
pubs.publication-statusPublished
pubs.volume7
pubs.embargo.termsNot known
icr.researchteamMolecular Oncology
dc.contributor.icrauthorBabina, Irina
dc.contributor.icrauthorTurner, Nicholas


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