Polymorphisms of DNA repair genes:: ERCC1 G19007A and ERCC2/XPD C22541A in a northeastern Chinese population

被引:12
作者
Yin, JY
Li, JC [1 ]
Vogel, U
Wang, HW
机构
[1] Zhejiang Univ, Inst Cell Biol, Hangzhou 310031, Peoples R China
[2] Shenyang Med Coll, Dept Med Genet, Shenyang 110034, Liaoning, Peoples R China
[3] Natl Inst Occupat Hlth, DK-2100 Copenhagen, Denmark
[4] Shenyang Med Coll, Dept Epidemiol, Shenyang 110034, Liaoning, Peoples R China
关键词
DNA repair genes; ERCC1; G19007A; ERCC2/XPD C22541A; genetic polymorphism; Chinese population;
D O I
10.1007/s10528-005-8170-3
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
DNA repair systems are responsible for maintaining the integrity of the genome and have a critical role in protecting against mutations that can lead to cancer. DNA repair gene products of ERCC1 and ERCC2/XPD are involved in the nucleotide excision repair pathway. The allele frequencies of the polymorphisms ERCC1 G19007A and ERCC2/XPD C22541A were examined in a northeastern Chinese population. The allele frequencies were 0.21 (A) and 0.79 (G) for ERCC1 G19007A and 0.49 (A) and 0.51 (C) for ERCC2/XPD C22541A. Comparison with average frequencies from previously reported Caucasian studies demonstrated that the A-allele frequency of ERCC1 G19007A was much lower in the northeastern Chinese population, indicating a remarkable ethnic difference (chi((1))(2) = 160.09, p < 0.001), and that allele frequencies of ERCC2/XPD C22541A showed marginal racial differences (chi((1))(2) = 4.36, p = 0.04). We have previously reported that both homozygote carriers of the A-allele as well as homozygous carriers of a high-risk haplotype (which includes the AA genotype in ERCC1 G19007A) were at increased risk of basal cell carcinoma, breast cancer, and lung cancer among Caucasians. The low A-allele frequency of ERCC1 G19007A in the Chinese population may suggest that the genetic contribution to cancer risk differs substantially between ethnic groups.
引用
收藏
页码:543 / 548
页数:6
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