Please use this identifier to cite or link to this item: http://hdl.handle.net/2445/201706
Title: Probing the diabetes and colorectal cancer relationship using gene – environment interaction analyses
Author: Dimou, Niki
Kim, Andre E.
Flanagan, Orlagh
Murphy, Neil
Díez Obrero, Virginia
Carreras Torres, Robert
Moreno Aguado, Víctor
Obón Santacana, Mireia
Kundaje, Anshul
Hsu, Li
Gauderman, W. James
Gunter, Marc J.
Peters, Ulrike
Keywords: Càncer colorectal
Diabetis
Colorectal cancer
Diabetes
Issue Date: 26-Jun-2023
Publisher: Springer Science and Business Media LLC
Abstract: BackgroundDiabetes 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.
Note: Reproducció del document publicat a: https://doi.org/10.1038/s41416-023-02312-z
It is part of: British Journal of Cancer, 2023, vol. 129, num. 3, p. 511-520
URI: http://hdl.handle.net/2445/201706
Related resource: https://doi.org/10.1038/s41416-023-02312-z
ISSN: 1532-1827
Appears in Collections:Articles publicats en revistes (Institut d'lnvestigació Biomèdica de Bellvitge (IDIBELL))

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