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dc.contributor.authorDutt, Amit
dc.contributor.authorRamos, Alex H.
dc.contributor.authorHammerman, Peter S.
dc.contributor.authorMermel, Craig H.
dc.contributor.authorCho, Jeonghee
dc.contributor.authorSharifnia, Tanaz
dc.contributor.authorChande, Ajit
dc.contributor.authorTanaka, Kumiko Elisa
dc.contributor.authorStransky, Nicolas
dc.contributor.authorGreulich, Heidi
dc.contributor.authorGray, Nathanael S.
dc.contributor.authorMeyerson, Matthew L.
dc.date.accessioned2011-10-24T21:17:07Z
dc.date.available2011-10-24T21:17:07Z
dc.date.issued2011-06
dc.date.submitted2010-12
dc.identifier.issn1932-6203
dc.identifier.urihttp://hdl.handle.net/1721.1/66570
dc.description.abstractBackground Squamous cell lung carcinomas account for approximately 25% of new lung carcinoma cases and 40,000 deaths per year in the United States. Although there are multiple genomically targeted therapies for lung adenocarcinoma, none has yet been reported in squamous cell lung carcinoma. Methodology/Principal Findings Using SNP array analysis, we found that a region of chromosome segment 8p11-12 containing three genes–WHSC1L1, LETM2, and FGFR1–is amplified in 3% of lung adenocarcinomas and 21% of squamous cell lung carcinomas. Furthermore, we demonstrated that a non-small cell lung carcinoma cell line harboring focal amplification of FGFR1 is dependent on FGFR1 activity for cell growth, as treatment of this cell line either with FGFR1-specific shRNAs or with FGFR small molecule enzymatic inhibitors leads to cell growth inhibition. Conclusions/Significance These studies show that FGFR1 amplification is common in squamous cell lung cancer, and that FGFR1 may represent a promising therapeutic target in non-small cell lung cancer.en_US
dc.description.sponsorshipNovartis Pharmaceuticals Corporationen_US
dc.description.sponsorshipAmerican Lung Associationen_US
dc.description.sponsorshipUniting Against Lung Canceren_US
dc.description.sponsorshipSara Thomas Monopoli Funden_US
dc.description.sponsorshipSeaman Foundationen_US
dc.description.sponsorshipIndia. Dept. of Biotechnologyen_US
dc.description.sponsorshipNational Lung Cancer Partnershipen_US
dc.language.isoen_US
dc.publisherPublic Library of Scienceen_US
dc.relation.isversionofhttp://dx.doi.org/10.1371/journal.pone.0020351en_US
dc.rightsCreative Commons Attributionen_US
dc.rights.urihttp://creativecommons.org/licenses/by/2.5/en_US
dc.sourcePLoSen_US
dc.titleInhibitor-Sensitive FGFR1 Amplification in Human Non-Small Cell Lung Canceren_US
dc.typeArticleen_US
dc.identifier.citationDutt, Amit et al. “Inhibitor-Sensitive FGFR1 Amplification in Human Non-Small Cell Lung Cancer.” Ed. Ming You. PLoS ONE 6 (2011): e20351.en_US
dc.contributor.departmentWhitaker College of Health Sciences and Technologyen_US
dc.contributor.departmentBroad Institute of MIT and Harvarden_US
dc.contributor.departmentHarvard University--MIT Division of Health Sciences and Technologyen_US
dc.contributor.approverMeyerson, Matthew L.
dc.contributor.mitauthorMeyerson, Matthew L.
dc.contributor.mitauthorDutt, Amit
dc.contributor.mitauthorRamos, Alex H.
dc.contributor.mitauthorMermel, Craig H.
dc.contributor.mitauthorTanaka, Kumiko Elisa
dc.contributor.mitauthorStransky, Nicolas
dc.contributor.mitauthorGreulich, Heidi
dc.contributor.mitauthorSharifnia, Tanaz
dc.relation.journalPLoS ONEen_US
dc.eprint.versionFinal published versionen_US
dc.type.urihttp://purl.org/eprint/type/JournalArticleen_US
eprint.statushttp://purl.org/eprint/status/PeerRevieweden_US
dspace.orderedauthorsDutt, Amit; Ramos, Alex H.; Hammerman, Peter S.; Mermel, Craig; Cho, Jeonghee; Sharifnia, Tanaz; Chande, Ajit; Tanaka, Kumiko Elisa; Stransky, Nicolas; Greulich, Heidi; Gray, Nathanael S.; Meyerson, Matthewen
mit.licensePUBLISHER_CCen_US
mit.metadata.statusComplete


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