4.7 Article

Genetic variants in CYP2B6 and HSD17B12 associated with risk of squamous cell carcinoma of the head and neck

期刊

INTERNATIONAL JOURNAL OF CANCER
卷 151, 期 4, 页码 553-564

出版社

WILEY
DOI: 10.1002/ijc.34023

关键词

GWAS; molecular epidemiology; PAH metabolism; SNP; squamous cell carcinoma of the head and neck; tobacco-specific nitrosamines

类别

资金

  1. Cancer Prevention and Research Institute of Texas [RP170259]
  2. National Institute of Environmental Health Sciences [R01 ES025460-01]
  3. National Institutes of Health [R01 ES011740, R01CA 131274, 1R01CA131324, R01DE022891]
  4. UICC Yamagiwa-Yoshida
  5. National Cancer Institute of Canada
  6. AIRC
  7. PAHO/WHO
  8. IARC Oral Cancer Multicenter study: Spain [BAE 01/5013, FIS 97/0662, FIS 97/0024]
  9. IARC Oral Cancer Multicenter study: Europe against Cancer [S06 96 202 489 05F02]
  10. IARC Central Europe study: INCO-COPERNICUS Program [WCRF99A28, NCI CA92039, IC15-CT98-0332]
  11. Fundacao De Amparo A Pesquisa Do Estado De Sao Paulo [01/01768-]
  12. Fondo para la Investigacion Cientifica y Tecnologica (Argentina)
  13. European Commission [INCO-DC IC18-CT97-0222]
  14. Fondazione Veronesi
  15. Rome Study [IG2013 14 220, IG2011 10 491]
  16. FIRMS
  17. Region Piemonte
  18. Padova University [CPDA057222]
  19. European Commission's 5th Framework Program [QLK1-2001-00182]
  20. Toronto study: the Canadian Cancer Society Research Institute [NCI U19 CA148127, 020214]
  21. GENCAPO: FAPESP [10/51168-0, 04/12054-9]
  22. Carolina Head and Neck Cancer Study (CHANCE) [R01-CA90731]
  23. University of Pittsburgh head and neck cancer study [P30 CA047904, P50 CA097190]
  24. U.S. National Cancer Institute (NCI) for genotyping for shared controls with the Lung OncoArray initiative [X01HG007492]
  25. U.S. National Institute of Dental and Craniofacial Research (NIDCR) [X01HG007780, U01 HG004446]
  26. National Institute on Alcohol Abuse and Alcoholism
  27. National Institute on Drug Abuse
  28. NIH contract
  29. Family Study of Cocaine Dependence (FSCD) [R01 DA013423]
  30. Collaborative Genetic Study of Nicotine Dependence (COGEND) [P01 CA089392]
  31. Collaborative Study on the Genetics of Alcoholism (COGA) [U10 AA008401]
  32. GENEVA Coordinating Center
  33. NIH Genes, Environment and Health Initiative [GEI] [U01HG004438, U01HG004422]
  34. Duke Cancer Institute as part of the P30 Cancer Center Support Grant [NIH/NCI CA014236]
  35. Fundacao de Amparo a Pesquisa do Estado de Sao Paulo (FAPESP) [04/12054-9, 10/51168-0] Funding Source: FAPESP

向作者/读者索取更多资源

This study assessed the associations between genetic variants in genes involved in the metabolism of PAHs and TSNA and the risk of squamous cell carcinoma of the head and neck (SCCHN) in European populations. The results showed significant associations between certain genetic variants and the risk of SCCHN, oropharyngeal cancer, and oral cancer. Additionally, the study revealed correlations between these genes and risks of other cancers, smoking behavior, and alcohol dependence.
Polycyclic aromatic hydrocarbons (PAH) and tobacco-specific nitrosamines (TSNA) metabolism-related genes play an important role in the development of cancers. We assessed the associations of genetic variants in genes involved in the metabolism of PAHs and TSNA with risk of squamous cell carcinoma of the head and neck (SCCHN) in European populations using two published genome-wide association study datasets. In the single-locus analysis, we identified two SNPs (rs145533669 and rs35246205) in CYP2B6 to be associated with risk of SCCHN (P = 1.57 x 10(-4) and .004, respectively), two SNPs (EPHX1 rs117522494 and CYP2B6 rs145533669) to be associated with risk of oropharyngeal cancer (P = .001 and .004, respectively), and one SNP (rs4359199 in HSD17B12) to be associated with risk of oral cancer (P = .006). A significant interaction effect was found between rs4359199 and drinking status on risks of SCCHN and oropharyngeal cancer (P < .05). eQTL and sQTL analyzes revealed that two SNPs (CYP2B6 rs35246205 and HSD17B12 rs4359199) were correlated with alternative splicing or mRNA expression levels of the corresponding genes in liver cells (P < .05 for both). In silico functional annotation suggested that these two SNPs may regulate mRNA expression by affecting the binding of transcription factors. Results from phenome-wide association studies presented significant associations between these genes and risks of other cancers, smoking behavior and alcohol dependence (P < .05). Thus, our study provided some insight into the underlying genetic mechanism of head and neck cancer, which warrants future functional validation.

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