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

Author:

Dimou NikiORCID,Kim Andre E.,Flanagan Orlagh,Murphy NeilORCID,Diez-Obrero Virginia,Shcherbina Anna,Aglago Elom K.ORCID,Bouras EmmanouilORCID,Campbell Peter T.,Casey Graham,Gallinger Steven,Gruber Stephen B.,Jenkins Mark A.,Lin Yi,Moreno VictorORCID,Ruiz-Narvaez EdwardORCID,Stern Mariana C.,Tian Yu,Tsilidis Kostas K.,Arndt VolkerORCID,Barry Elizabeth L.,Baurley James W.,Berndt Sonja I.,Bézieau Stéphane,Bien Stephanie A.,Bishop D. TimothyORCID,Brenner HermannORCID,Budiarto Arif,Carreras-Torres Robert,Cenggoro Tjeng Wawan,Chan Andrew T.ORCID,Chang-Claude Jenny,Chanock Stephen J.,Chen XuechenORCID,Conti David V.,Dampier Christopher H.,Devall Matthew,Drew David A.,Figueiredo Jane C.,Giles Graham G.,Gsur Andrea,Harrison Tabitha A.,Hidaka Akihisa,Hoffmeister MichaelORCID,Huyghe Jeroen R.ORCID,Jordahl Kristina,Kawaguchi Eric,Keku Temitope O.,Larsson Susanna C.ORCID,Le Marchand Loic,Lewinger Juan Pablo,Li Li,Mahesworo Bharuno,Morrison John,Newcomb Polly A.ORCID,Newton Christina C.,Obon-Santacana Mireia,Ose Jennifer,Pai Rish K.,Palmer Julie R.ORCID,Papadimitriou Nikos,Pardamean Bens,Peoples Anita R.,Pharoah Paul D. P.ORCID,Platz Elizabeth A.,Potter John D.ORCID,Rennert Gad,Scacheri Peter C.,Schoen Robert E.,Su Yu-Ru,Tangen Catherine M.,Thibodeau Stephen N.,Thomas Duncan C.,Ulrich Cornelia M.,Um Caroline Y.ORCID,van Duijnhoven Franzel J. B.,Visvanathan KalaORCID,Vodicka Pavel,Vodickova Ludmila,White Emily,Wolk AlicjaORCID,Woods Michael O.,Qu Conghui,Kundaje AnshulORCID,Hsu Li,Gauderman W. James,Gunter Marc J.,Peters Ulrike

Abstract

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-value3-d.f.: 5.46 × 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-value2-d.f.: 7.84 × 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.

Funder

Cancer Research UK

Publisher

Springer Science and Business Media LLC

Subject

Cancer Research,Oncology

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