Probing the diabetes and colorectal cancer relationship using gene – environment interaction analyses
Background Diabetes 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 in...
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Veröffentlicht in: | British journal of cancer 2023-08, Vol.129 (3), p.511-520 |
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Sprache: | eng |
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Zusammenfassung: | Background
Diabetes 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.
Methods
We 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).
Results
Based 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 –
OR
AA
: 1.62, 95% CI: 1.34–1.96; OR
AG
: 1.41, 95% CI: 1.30–1.54; OR
GG
: 1.22, 95% CI: 1.13–1.31;
p
-value
3-d.f.
: 5.46 × 10
−11
) and 13q14.13 (rs9526201,
LRCH1 –
OR
GG
: 2.11, 95% CI: 1.56–2.83; OR
GA
: 1.52, 95% CI: 1.38–1.68; OR
AA
: 1.13, 95% CI: 1.06–1.21;
p
-value
2-d.f.
: 7.84 × 10
−09
).
Discussion
These 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. |
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ISSN: | 0007-0920 1532-1827 1532-1827 |
DOI: | 10.1038/s41416-023-02312-z |