Probing the diabetes and colorectal cancer relationship using gene – environment interaction analyses

dc.contributor.authorDimou, Niki
dc.contributor.authorKim, Andre E.
dc.contributor.authorFlanagan, Orlagh
dc.contributor.authorMurphy, Neil
dc.contributor.authorDíez Obrero, Virginia
dc.contributor.authorCarreras Torres, Robert
dc.contributor.authorMoreno Aguado, Víctor
dc.contributor.authorObón Santacana, Mireia
dc.contributor.authorKundaje, Anshul
dc.contributor.authorHsu, Li
dc.contributor.authorGauderman, W. James
dc.contributor.authorGunter, Marc J.
dc.contributor.authorPeters, Ulrike
dc.date.accessioned2023-09-04T14:33:05Z
dc.date.available2023-09-04T14:33:05Z
dc.date.issued2023-06-26
dc.date.updated2023-09-04T13:37:09Z
dc.description.abstractBackgroundDiabetes is an established risk factor for colorectal cancer. However, the mechanisms underlying this relationship still require investigation and it is not known if the association is modified by genetic variants. To address these questions, we undertook a genome-wide gene-environment interaction analysis.MethodsWe used data from 3 genetic consortia (CCFR, CORECT, GECCO; 31,318 colorectal cancer cases/41,499 controls) and undertook genome-wide gene-environment interaction analyses with colorectal cancer risk, including interaction tests of genetics(G)xdiabetes (1-degree of freedom; d.f.) and joint testing of Gxdiabetes, G-colorectal cancer association (2-d.f. joint test) and G-diabetes correlation (3-d.f. joint test).ResultsBased on the joint tests, we found that the association of diabetes with colorectal cancer risk is modified by loci on chromosomes 8q24.11 (rs3802177, SLC30A8 - ORAA: 1.62, 95% CI: 1.34-1.96; ORAG: 1.41, 95% CI: 1.30-1.54; ORGG: 1.22, 95% CI: 1.13-1.31; p-value(3-d.f.): 5.46 x 10(-11)) and 13q14.13 (rs9526201, LRCH1 - ORGG: 2.11, 95% CI: 1.56-2.83; ORGA: 1.52, 95% CI: 1.38-1.68; ORAA: 1.13, 95% CI: 1.06-1.21; p-value(2-d.f.): 7.84 x 10(-09)).DiscussionThese results suggest that variation in genes related to insulin signaling (SLC30A8) and immune function (LRCH1) may modify the association of diabetes with colorectal cancer risk and provide novel insights into the biology underlying the diabetes and colorectal cancer relationship.
dc.format.extent10 p.
dc.format.mimetypeapplication/pdf
dc.identifier.issn1532-1827
dc.identifier.pmid37365285
dc.identifier.urihttps://hdl.handle.net/2445/201706
dc.language.isoeng
dc.publisherSpringer Science and Business Media LLC
dc.relation.isformatofReproducció del document publicat a: https://doi.org/10.1038/s41416-023-02312-z
dc.relation.ispartofBritish Journal of Cancer, 2023, vol. 129, num. 3, p. 511-520
dc.relation.urihttps://doi.org/10.1038/s41416-023-02312-z
dc.rightscc by-nc (c) Dimou, Niki et al, 2023
dc.rights.accessRightsinfo:eu-repo/semantics/openAccess
dc.rights.urihttp://creativecommons.org/licenses/by-nc/3.0/es/*
dc.sourceArticles publicats en revistes (Institut d'lnvestigació Biomèdica de Bellvitge (IDIBELL))
dc.subject.classificationCàncer colorectal
dc.subject.classificationDiabetis
dc.subject.otherColorectal cancer
dc.subject.otherDiabetes
dc.titleProbing the diabetes and colorectal cancer relationship using gene – environment interaction analyses
dc.typeinfo:eu-repo/semantics/article
dc.typeinfo:eu-repo/semantics/publishedVersion

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