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PMID: 15849729 Published · ppublish English Journal Article

Polymorphisms in the DNA nucleotide excision repair genes and lung cancer risk in Xuan Wei, China.

International journal of cancer ·Vol. 116 ·No. 5 ·2005-09-20 ·Pages 768-73

Shen M, Berndt SI, Rothman N, Demarini DM, Mumford JL, He X, Bonner MR, Tian L, Yeager M, Welch R, Chanock S, Zheng T, Caporaso N, Lan Q

Abstract

The lung cancer mortality rate in Xuan Wei County is among the highest in China and has been attributed to exposure to indoor smoky coal emissions that contain very high levels of polycyclic aromatic hydrocarbons (PAHs). Nucleotide excision repair (NER) plays a key role in reversing DNA damage from exposure to environmental carcinogens, such as PAHs, that form bulky DNA adducts. We studied single nucleotide polymorphisms (SNPs) and their corresponding haplotypes in 6 genes (ERCC1, ERCC2/XPD, ERCC4/XPF, ERCC5/XPG, RAD23B and XPC) involved in NER in a population-based case-control study of lung cancer in Xuan Wei. A total of 122 incident primary lung cancer cases and 122 individually matched controls were enrolled. Three linked SNPs in ERCC2 were associated with lung cancer with similar ORs; e.g., persons with the Gln allele at codon 751 had a 60% reduction of lung cancer (OR = 0.40, 95% CI 0.18-0.89). Moreover, one haplotype in ERCC2 was associated with a decreased risk of lung cancer (OR = 0.40, 95% CI 0.19-0.85) compared to the most common haplotype. In addition, subjects with one or 2 copies of the Val allele at codon 249 of RAD23B had a 2-fold increased risk of lung cancer (OR = 1.91, 95% CI 1.12-3.24). In summary, our results suggest that genetic variants in genes involved in the NER pathway may play a role in lung cancer susceptibility in Xuan Wei. However, due to the small sample size, additional studies are needed to evaluate these associations within Xuan Wei and in other populations with substantial environmental exposure to PAHs.

MeSH Terms
Adult Aged Case-Control Studies DNA Helicases/genetics DNA Repair/genetics DNA Repair Enzymes DNA-Binding Proteins/genetics Endonucleases/genetics Female Humans Linkage Disequilibrium Lung Neoplasms/etiology,genetics Male Middle Aged Nuclear Proteins/genetics Polymorphism, Single Nucleotide Risk Transcription Factors/genetics Xeroderma Pigmentosum Group D Protein
Chemicals
DNA excision repair protein ERCC-5 DNA-Binding Proteins Nuclear Proteins RAD23B protein, human Transcription Factors xeroderma pigmentosum group F protein RAD23A protein, human XPC protein, human ERCC1 protein, human Endonucleases DNA Helicases Xeroderma Pigmentosum Group D Protein ERCC2 protein, human DNA Repair Enzymes
Authors & Affiliations
14 authors, click to expand affiliations / ORCID
Shen Min
Division of Cancer Epidemiology and Genetics, National Cancer Institute, National Institutes of Health, Bethesda, MD 20892-7240, USA. shenmi@mail.nih.gov
Berndt Sonja I
Rothman Nathaniel
Demarini David M
Mumford Judy L
He Xingzhou
Bonner Matthew R
Tian Linwei
Yeager Meredith
Welch Robert
Chanock Stephen
Zheng Tongzhang
Caporaso Neil
Lan Qing
Article Info
Journal
International journal of cancer
Abbr.
Int J Cancer
ISSN
0020-7136
Published
2005-09-20
Pages
768-73
Language
English
Region
United States
NLM ID
0042124
Subset
IM
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