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TTF1 expression in non-small cell lung carcinoma: association with TTF1 gene amplification and improved survival No conflicts of interest were declared.

dc.contributor.authorPerner, Svenen_US
dc.contributor.authorWagner, P. L.en_US
dc.contributor.authorSoltermann, A.en_US
dc.contributor.authorLaFargue, C.en_US
dc.contributor.authorTischler, V.en_US
dc.contributor.authorWeir, Barbara A.en_US
dc.contributor.authorWeder, W.en_US
dc.contributor.authorMeyerson, M.en_US
dc.contributor.authorGiordano, Thomas J.en_US
dc.contributor.authorMoch, H.en_US
dc.contributor.authorRubin, Mark A.en_US
dc.date.accessioned2009-01-07T15:29:29Z
dc.date.available2010-03-01T21:10:29Zen_US
dc.date.issued2009-01en_US
dc.identifier.citationPerner, S; Wagner, PL; Soltermann, A; LaFargue, C; Tischler, V; Weir, BA; Weder, W; Meyerson, M; Giordano, TJ; Moch, H; Rubin, MA (2009). "TTF1 expression in non-small cell lung carcinoma: association with TTF1 gene amplification and improved survival No conflicts of interest were declared. ." The Journal of Pathology 217(1): 65-72. <http://hdl.handle.net/2027.42/61439>en_US
dc.identifier.issn0022-3417en_US
dc.identifier.issn1096-9896en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/61439
dc.identifier.urihttp://www.ncbi.nlm.nih.gov/sites/entrez?cmd=retrieve&db=pubmed&list_uids=18932182&dopt=citationen_US
dc.description.abstractAcquired chromosomal aberrations play an important role in tumour development and progression. Such genetic alterations occur in a significant proportion of non-small cell lung carcinomas (NSCLCs) and include amplification of 14q13.3, which contains the TTF1 gene. We asked whether TTF1 amplification is associated with increased TTF1 protein expression in NSCLCs, and whether TTF1 is associated with clinicopathological features, including patient survival. We used a FISH assay and quantitative immunohistochemical staining to interrogate a population-based cohort of 538 NSCLCs from Swiss patients for TTF1 amplification and protein expression. We found TTF1 amplification in ∼13% of adenocarcinomas (ACs) and in ∼9% of squamous cell carcinomas (SCCs) and TTF1 amplification was associated with increased TTF1 protein expression. High-level TTF1 expression was significantly associated with smaller tumour size, female gender and longer overall survival only among ACs (median survival 82 versus 28 months; p = 0.002). On multivariate analysis, high TTF1 expression was an independent predictor of favourable prognosis in patients with AC [hazard ratio, 0.56 (95% CI 0.38–0.83); p = 0.008]. We conclude that TTF1 amplification is a mechanism of high-level TTF1 expression in a subset of NSCLCs. When expressed at high levels, this routinely used diagnostic marker is also an independent biomarker of favourable prognosis in AC. Copyright © 2008 Pathological Society of Great Britain and Ireland. Published by John Wiley & Sons, Ltd.en_US
dc.format.extent276273 bytes
dc.format.extent3118 bytes
dc.format.mimetypeapplication/pdf
dc.format.mimetypetext/plain
dc.publisherJohn Wiley & Sons, Ltd.en_US
dc.subject.otherLife and Medical Sciencesen_US
dc.subject.otherCancer Research, Oncology and Pathologyen_US
dc.titleTTF1 expression in non-small cell lung carcinoma: association with TTF1 gene amplification and improved survival No conflicts of interest were declared.en_US
dc.typeArticleen_US
dc.rights.robotsIndexNoFollowen_US
dc.subject.hlbsecondlevelPathologyen_US
dc.subject.hlbtoplevelHealth Sciencesen_US
dc.description.peerreviewedPeer Revieweden_US
dc.contributor.affiliationumDepartment of Pathology, Comprehensive Cancer Center, University of Michigan Medical School, Ann Arbor, MI, USAen_US
dc.contributor.affiliationotherDepartment of Pathology and Laboratory Medicine, Weill Cornell Medical Center, New York, NY, USA ; SP and PW contributed equally to this study and should both be considered first authors.en_US
dc.contributor.affiliationotherDepartment of Pathology and Laboratory Medicine, Weill Cornell Medical Center, New York, NY, USAen_US
dc.contributor.affiliationotherInstitute of Surgical Pathology, Department of Pathology, University Hospital of Zurich, Zurich, Switzerlanden_US
dc.contributor.affiliationotherDepartment of Pathology and Laboratory Medicine, Weill Cornell Medical Center, New York, NY, USAen_US
dc.contributor.affiliationotherInstitute of Surgical Pathology, Department of Pathology, University Hospital of Zurich, Zurich, Switzerlanden_US
dc.contributor.affiliationotherDepartment of Medical Oncology, Center for Cancer Genome Discovery, Dana-Farber Cancer Institute, Boston, MA, USA ; Broad Institute of Harvard and M.I.T, Cambridge, MA, USAen_US
dc.contributor.affiliationotherDivision of Thoracic Surgery, University Hospital of Zurich, Zurich, Switzerlanden_US
dc.contributor.affiliationotherDepartment of Medical Oncology, Center for Cancer Genome Discovery, Dana-Farber Cancer Institute, Boston, MA, USA ; Broad Institute of Harvard and M.I.T, Cambridge, MA, USA ; Department of Pathology, Harvard Medical School, Boston, MA, USAen_US
dc.contributor.affiliationotherInstitute of Surgical Pathology, Department of Pathology, University Hospital of Zurich, Zurich, Switzerlanden_US
dc.contributor.affiliationotherDepartment of Pathology and Laboratory Medicine, Weill Cornell Medical Center, New York, NY, USA ; Department of Pathology and Laboratory Medicine, Weill Cornell Medical Center, New York, NY, USA.en_US
dc.identifier.pmid18932182en_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/61439/1/2443_ftp.pdf
dc.identifier.doihttp://dx.doi.org/10.1002/path.2443en_US
dc.identifier.sourceThe Journal of Pathologyen_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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