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dc.contributor.authorLópez de Maturana, Evangelina-
dc.contributor.authorNavarro, Arcadi-
dc.contributor.authorLorente-Galdós, Belén-
dc.contributor.authorMalats, Núria-
dc.date.accessioned2015-02-27T13:10:51Z-
dc.date.available2015-02-27T13:10:51Z-
dc.date.issued2013-12-31-
dc.identifierdoi: 10.1371/journal.pone.0083745-
dc.identifierissn: 1932-6203-
dc.identifier.citationPLoS ONE 8(12): e83745 (2013)-
dc.identifier.urihttp://hdl.handle.net/10261/111526-
dc.description.abstractThe relationship between inflammation and cancer is well established in several tumor types, including bladder cancer. We performed an association study between 886 inflammatory-gene variants and bladder cancer risk in 1,047 cases and 988 controls from the Spanish Bladder Cancer (SBC)/EPICURO Study. A preliminary exploration with the widely used univariate logistic regression approach did not identify any significant SNP after correcting for multiple testing. We further applied two more comprehensive methods to capture the complexity of bladder cancer genetic susceptibility: Bayesian Threshold LASSO (BTL), a regularized regression method, and AUC-Random Forest, a machine-learning algorithm. Both approaches explore the joint effect of markers. BTL analysis identified a signature of 37 SNPs in 34 genes showing an association with bladder cancer. AUC-RF detected an optimal predictive subset of 56 SNPs. 13 SNPs were identified by both methods in the total population. Using resources from the Texas Bladder Cancer study we were able to replicate 30% of the SNPs assessed. The associations between inflammatory SNPs and bladder cancer were reexamined among non-smokers to eliminate the effect of tobacco, one of the strongest and most prevalent environmental risk factor for this tumor. A 9 SNP-signature was detected by BTL. Here we report, for the first time, a set of SNP in inflammatory genes jointly associated with bladder cancer risk. These results highlight the importance of the complex structure of genetic susceptibility associated with cancer risk. © 2013 de Maturana et al.-
dc.description.sponsorshipThe work was partially supported by the Fondo de Investigación Sanitaria, Instituto de Salud Carlos III (G03/174, 00/0745, PI051436, PI061614, PI09-02102, G03/174 and Sara Borrell fellowship to ELM) and Ministry of Science and Innovation (MTM2008-06747-C02-02 and FPU fellowship award to VU), Spain; AGAUR-Generalitat de Catalunya (Grant 2009SGR-581); Fundacióla Maratóde TV3; Red Temática de Investigación Cooperativa en Cáncer (RTICC); Asociación Española Contra el Cáncer (AECC); EU-FP7-201663; and RO1- CA089715 and CA34627; the Spanish National Institute for Bioinformatics (www.inab.org); and by the Intramural Research Program of the Division of Cancer Epidemiology and Genetics, National Cancer Institute, USA. MD Anderson support for this project included U01 CA 127615 (XW); R01 CA 74880 (XW); P50 CA 91846 (XW, CPD); Betty B. Marcus Chair fund in Cancer Prevention (XW); UT Research Trust fund (XW) and R01 CA 131335 (JG).-
dc.publisherPublic Library of Science-
dc.relationinfo:eu-repo/grantAgreement/EC/FP7/201663-
dc.relation.isversionofPublisher's version-
dc.rightsopenAccess-
dc.titleApplication of multi-SNP approaches Bayesian LASSO and AUC-RF to detect main effects of inflammatory-gene variants associated with bladder cancer risk-
dc.typeartículo-
dc.identifier.doi10.1371/journal.pone.0083745-
dc.relation.publisherversionhttp://dx.doi.org/10.1371/journal.pone.0083745-
dc.date.updated2015-02-27T13:10:52Z-
dc.description.versionPeer Reviewed-
dc.language.rfc3066eng-
dc.rights.licensehttp://creativecommons.org/licenses/by/4.0/-
dc.contributor.funderInstituto de Salud Carlos III-
dc.contributor.funderMinisterio de Ciencia e Innovación (España)-
dc.contributor.funderGeneralitat de Catalunya-
dc.contributor.funderFundació La Marató de TV3-
dc.contributor.funderRed Temática de Investigación Cooperativa en Cáncer (España)-
dc.contributor.funderAsociación Española Contra el Cáncer-
dc.contributor.funderInstituto Nacional de Bioinformática (España)-
dc.contributor.funderNational Cancer Institute (US)-
dc.relation.csic-
dc.identifier.funderhttp://dx.doi.org/10.13039/501100004587es_ES
dc.identifier.funderhttp://dx.doi.org/10.13039/501100004837es_ES
dc.identifier.funderhttp://dx.doi.org/10.13039/501100002809es_ES
dc.identifier.funderhttp://dx.doi.org/10.13039/100008666es_ES
dc.identifier.pmid24391818-
dc.type.coarhttp://purl.org/coar/resource_type/c_6501es_ES
item.openairetypeartículo-
item.grantfulltextopen-
item.cerifentitytypePublications-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.fulltextWith Fulltext-
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