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Gene by Environment Investigation of Incident Lung Cancer Risk in African-Americans.

Authors :
David SP
Wang A
Kapphahn K
Hedlin H
Desai M
Henderson M
Yang L
Walsh KM
Schwartz AG
Wiencke JK
Spitz MR
Wenzlaff AS
Wrensch MR
Eaton CB
Furberg H
Mark Brown W
Goldstein BA
Assimes T
Tang H
Kooperberg CL
Quesenberry CP
Tindle H
Patel MI
Amos CI
Bergen AW
Swan GE
Stefanick ML
Source :
EBioMedicine [EBioMedicine] 2016 Jan 11; Vol. 4, pp. 153-61. Date of Electronic Publication: 2016 Jan 11 (Print Publication: 2016).
Publication Year :
2016

Abstract

Background: Genome-wide association studies have identified polymorphisms linked to both smoking exposure and risk of lung cancer. The degree to which lung cancer risk is driven by increased smoking, genetics, or gene-environment interactions is not well understood.<br />Methods: We analyzed associations between 28 single nucleotide polymorphisms (SNPs) previously associated with smoking quantity and lung cancer in 7156 African-American females in the Women's Health Initiative (WHI), then analyzed main effects of top nominally significant SNPs and interactions between SNPs, cigarettes per day (CPD) and pack-years for lung cancer in an independent, multi-center case-control study of African-American females and males (1078 lung cancer cases and 822 controls).<br />Findings: Nine nominally significant SNPs for CPD in WHI were associated with incident lung cancer (corrected p-values from 0.027 to 6.09 × 10(-5)). CPD was found to be a nominally significant effect modifier between SNP and lung cancer for six SNPs, including CHRNA5 rs2036527[A](betaSNP*CPD = - 0.017, p = 0.0061, corrected p = 0.054), which was associated with CPD in a previous genome-wide meta-analysis of African-Americans.<br />Interpretation: These results suggest that chromosome 15q25.1 variants are robustly associated with CPD and lung cancer in African-Americans and that the allelic dose effect of these polymorphisms on lung cancer risk is most pronounced in lighter smokers.

Details

Language :
English
ISSN :
2352-3964
Volume :
4
Database :
MEDLINE
Journal :
EBioMedicine
Publication Type :
Academic Journal
Accession number :
26981579
Full Text :
https://doi.org/10.1016/j.ebiom.2016.01.002