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

Publication ,  Journal Article
David, SP; Wang, A; Kapphahn, K; Hedlin, H; Desai, M; Henderson, M; Yang, L; Walsh, KM; Schwartz, AG; Wiencke, JK; Spitz, MR; Wenzlaff, AS ...
Published in: EBioMedicine
February 2016

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. 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). 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. 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.

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Published In

EBioMedicine

DOI

EISSN

2352-3964

Publication Date

February 2016

Volume

4

Start / End Page

153 / 161

Location

Netherlands

Related Subject Headings

  • Smoking
  • Receptors, Nicotinic
  • Polymorphism, Single Nucleotide
  • Nerve Tissue Proteins
  • Male
  • Lung Neoplasms
  • Humans
  • Genes, Modifier
  • Gene-Environment Interaction
  • Female
 

Citation

APA
Chicago
ICMJE
MLA
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David, S. P., Wang, A., Kapphahn, K., Hedlin, H., Desai, M., Henderson, M., … Stefanick, M. L. (2016). Gene by Environment Investigation of Incident Lung Cancer Risk in African-Americans. EBioMedicine, 4, 153–161. https://doi.org/10.1016/j.ebiom.2016.01.002
David, Sean P., Ange Wang, Kristopher Kapphahn, Haley Hedlin, Manisha Desai, Michael Henderson, Lingyao Yang, et al. “Gene by Environment Investigation of Incident Lung Cancer Risk in African-Americans.EBioMedicine 4 (February 2016): 153–61. https://doi.org/10.1016/j.ebiom.2016.01.002.
David SP, Wang A, Kapphahn K, Hedlin H, Desai M, Henderson M, et al. Gene by Environment Investigation of Incident Lung Cancer Risk in African-Americans. EBioMedicine. 2016 Feb;4:153–61.
David, Sean P., et al. “Gene by Environment Investigation of Incident Lung Cancer Risk in African-Americans.EBioMedicine, vol. 4, Feb. 2016, pp. 153–61. Pubmed, doi:10.1016/j.ebiom.2016.01.002.
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. Gene by Environment Investigation of Incident Lung Cancer Risk in African-Americans. EBioMedicine. 2016 Feb;4:153–161.
Journal cover image

Published In

EBioMedicine

DOI

EISSN

2352-3964

Publication Date

February 2016

Volume

4

Start / End Page

153 / 161

Location

Netherlands

Related Subject Headings

  • Smoking
  • Receptors, Nicotinic
  • Polymorphism, Single Nucleotide
  • Nerve Tissue Proteins
  • Male
  • Lung Neoplasms
  • Humans
  • Genes, Modifier
  • Gene-Environment Interaction
  • Female