ERCC2/XPD gene polymorphisms and lung cancer:: A HuGE review

被引:147
作者
Benhamou, S
Sarasin, A
机构
[1] Univ Evry, INSERM, EMI 00 06, F-91034 Evry, France
[2] Inst Gustave Roussy, CNRS, Unite Propre Rech 2169, Villejuif, France
关键词
epidemiology; ERCC-2; protein; ERCC2/XPD; genetics; lung neoplasms; polymorphism (genetics); xeroderma pigmentosum;
D O I
10.1093/aje/kwi018
中图分类号
R1 [预防医学、卫生学];
学科分类号
1004 ; 120402 ;
摘要
The xeroderma pigmentosum group D (XPD) protein is a well-characterized DNA helicase necessary for the nucleotide excision repair of bulky DNA lesions, such as those induced by cigarette smoking. Polymorphisms in several exons of the XPD gene have been identified; two of them, Asp312Asn and Lys751 Gln, are common and result in an amino acid change. Most of the reported data indicate higher levels of DNA adducts in people carrying variant Asn or Gln alleles, which suggests that these persons have lower repair efficiency. These two polymorphisms have been hypothesized to modify the risk of lung cancer. To examine this association, the authors undertook a review and meta-analyses of nine published case-control studies. No clear association between XPD Asp312Asn or XPD Lys751 Gln gene polymorphisms and lung cancer was found. However, it may be only the joint effect of multiple polymorphisms within the gene that provides information about an association with lung cancer. Because of advances in high-throughput genotyping techniques, it is likely that future association studies on lung cancer will need to investigate multiple polymorphisms within genes and multiple genes within the same pathway and will need to use recently developed haplotype-based methods to evaluate the haplotypic effects.
引用
收藏
页码:1 / 14
页数:14
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