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Large-scale association analysis identifies new lung cancer susceptibility loci and heterogeneity in genetic susceptibility across histological subtypes

dc.contributor.authorMcKay, James D.
dc.contributor.authorHung, Rayjean J.
dc.contributor.authorHan, Younghun
dc.contributor.authorZong, Xuchen
dc.contributor.authorCarreras-Torres, Robert
dc.contributor.authorChristiani, David C.
dc.contributor.authorCaporaso, Neil E.
dc.contributor.authorJohansson, Mattias
dc.contributor.authorTardón García, Adonina 
dc.contributor.authorFernández Somoano, Ana 
dc.contributor.authorFernández Tardón, Guillermo 
dc.date.accessioned2017-07-20T07:24:50Z
dc.date.available2017-07-20T07:24:50Z
dc.date.issued2017
dc.identifier.citationNature Genetics, 49(7), p.1126-1132 (2017); doi:10.1038/ng.3892
dc.identifier.issn1061-4036
dc.identifier.issn1546-1718
dc.identifier.urihttp://hdl.handle.net/10651/43496
dc.description.abstractAlthough several lung cancer susceptibility loci have been identified, much of the heritability for lung cancer remains unexplained. Here 14,803 cases and 12,262 controls of European descent were genotyped on the OncoArray and combined with existing data for an aggregated genome-wide association study (GWAS) analysis of lung cancer in 29,266 cases and 56,450 controls. We identified 18 susceptibility loci achieving genome-wide significance, including 10 new loci. The new loci highlight the striking heterogeneity in genetic susceptibility across the histological subtypes of lung cancer, with four loci associated with lung cancer overall and six loci associated with lung adenocarcinoma. Gene expression quantitative trait locus (eQTL) analysis in 1,425 normal lung tissue samples highlights RNASET2, SECISBP2L and NRG1 as candidate genes. Other loci include genes such as a cholinergic nicotinic receptor, CHRNA2, and the telomere-related genes OFBC1 and RTEL1. Further exploration of the target genes will continue to provide new insights into the etiology of lung cancereng
dc.description.sponsorshipCentre for Inherited Disease Research [26820120008i-0-26800068-1]; Fondation de l'Institut Universitaire de Cardiologie et de Pneumologie de Quebec; Respiratory Health Network of the FRQS; Canadian Institutes of Health Research [MOP-123369]; [U19-CA148127]; [CA148127S1]
dc.description.statementofresponsibilityMcKay, J.D., Hung, R.J., Han, Y., Zong, X., Carreras-Torres, R., Christiani, D.C., Caporaso, N.E., Johansson, M., Xiao, X., Li, Y., Byun, J., Dunning, A., Pooley, K.A., Qian, D.C., Ji, X., Liu, G., Timofeeva, M.N., Bojesen, S.E., Wu, X., Marchand, L.L., Albanes, D., Bickeböller, H., Aldrich, M.C., Bush, W.S., Tardon, A., Rennert, G., Teare, M.D., Field, J.K., Kiemeney, L.A., Lazarus, P., Haugen, A., Lam, S., Schabath, M.B., Andrew, A.S., Shen, H., Hong, Y.-C., Yuan, J.-M., Bertazzi, P.A., Pesatori, A.C., Ye, Y., Diao, N., Su, L., Zhang, R., Brhane, Y., Leighl, N., Johansen, J.S., Mellemgaard, A., Saliba, W., Haiman, C.A., Wilkens, L.R., Fernandez-Somoano, A., Fernandez-Tardon, G., Van Der Heijden, H.F.M., Kim, J.H., Dai, J., Hu, Z., Davies, M.P.A., Marcus, M.W., Brunnström, H., Manjer, J., Melander, O., Muller, D.C., Overvad, K., Trichopoulou, A., Tumino, R., Doherty, J.A., Barnett, M.P., Chen, C., Goodman, G.E., Cox, A., Taylor, F., Woll, P., Brüske, I., Wichmann, H.-E., Manz, J., Muley, T.R., Risch, A., Rosenberger, A., Grankvist, K., Johansson, M., Shepherd, F.A., Tsao, M.-S., Arnold, S.M., Haura, E.B., Bolca, C., Holcatova, I., Janout, V., Kontic, M., Lissowska, J., Mukeria, A., Ognjanovic, S., Orlowski, T.M., Scelo, G., Swiatkowska, B., Zaridze, D., Bakke, P., Skaug, V., Zienolddiny, S., Duell, E.J., Butler, L.M., Koh, W.-P., Gao, Y.-T., Houlston, R.S., McLaughlin, J., Stevens, V.L., Joubert, P., Lamontagne, M., Nickle, D.C., Obeidat, M., Timens, W., Zhu, B., Song, L., Kachuri, L., Artigas, M.S., Tobin, M.D., Wain, L.V., Rafnar, T., Thorgeirsson, T.E., Reginsson, G.W., Stefansson, K., Hancock, D.B., Bierut, L.J., Spitz, M.R., Gaddis, N.C., Lutz, S.M., Gu, F., Johnson, E.O., Kamal, A., Pikielny, C., Zhu, D., Lindströem, S., Jiang, X., Tyndale, R.F., Chenevix-Trench, G., Beesley, J., Bossé, Y., Chanock, S., Brennan, P., Landi, M.T., Amos, C.I.
dc.format.extentp. 1126-1132spa
dc.language.isoengspa
dc.relation.ispartofNature Genetics, 49(7)spa
dc.titleLarge-scale association analysis identifies new lung cancer susceptibility loci and heterogeneity in genetic susceptibility across histological subtypeseng
dc.typejournal articlespa
dc.identifier.doi10.1038/ng.3892
dc.relation.publisherversionhttp://dx.doi.org/10.1038/ng.3892


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