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DNA修复基因多态性:中国东北人群中的ERCC1 G19007A和ERCC2/XPD C22541A

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

作者信息

Yin Jiaoyang, Li Jicheng, Vogel Ulla, Wang Huiwen

机构信息

Institute of Cell Biology, Zhejiang University, Hangzhou, 310031, Zhejiang, P.R. China.

出版信息

Biochem Genet. 2005 Oct;43(9-10):543-8. doi: 10.1007/s10528-005-8170-3.

Abstract

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.

摘要

DNA修复系统负责维持基因组的完整性,并在预防可能导致癌症的突变方面发挥关键作用。ERCC1和ERCC2/XPD的DNA修复基因产物参与核苷酸切除修复途径。在中国东北人群中检测了ERCC1 G19007A和ERCC2/XPD C22541A多态性的等位基因频率。ERCC1 G19007A的等位基因频率为0.21(A)和0.79(G),ERCC2/XPD C22541A的等位基因频率为0.49(A)和0.51(C)。与先前报道的高加索人研究的平均频率相比,表明中国东北人群中ERCC1 G19007A的A等位基因频率要低得多,这表明存在显著的种族差异(χ(1)(2)=160.09,p<0.001),并且ERCC2/XPD C22541A的等位基因频率显示出轻微的种族差异(χ(1)(2)=4.36,p=0.04)。我们先前曾报道,在高加索人中,A等位基因的纯合携带者以及高风险单倍型的纯合携带者(其中包括ERCC1 G19007A中的AA基因型)患基底细胞癌、乳腺癌和肺癌的风险增加。中国人群中ERCC1 G19007A的低A等位基因频率可能表明不同种族之间癌症风险的遗传贡献存在显著差异。

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