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DNA修复基因XRCC1的非同义单核苷酸多态性与宫颈癌发生及高危型人乳头瘤病毒感染易感性

The nonsynonymous single nucleotide polymorphisms of DNA repair gene XRCC1 and susceptibility to the development of cervical carcinoma and high-risk human papillomavirus infection.

作者信息

Huang J, Ye F, Chen H, Lu W, Xie X

机构信息

Women's Reproductive Health Laboratory of Zhejiang Province, Hangzhou, China.

出版信息

Int J Gynecol Cancer. 2007 May-Jun;17(3):668-75. doi: 10.1111/j.1525-1438.2007.00840.x.

Abstract

To evaluate contribution of single nucleotide polymorphisms (SNPs) of X-ray repair cross-complementing group 1 (XRCC1) gene to the risk of cervical carcinoma, we conducted a case-control study of 1012 patients including 539 carcinoma and 473 cervical intraepithelial neoplasia (CIN) and 800 normal women controls and genotyped three XRCC1 SNPs (Arg194Trp, Arg280His, and Arg399Gln). We found that compared with the Arg399Gln (GG), subjects carrying the homozygous Gln399Gln (AA) genotype had a significantly 2.32-fold increased risk of cervical carcinoma (95% CI 1.47-3.65), heterozygous Arg399Gln (GA) genotype were also associated with a significantly increased risk of cervical carcinoma, with the adjusted odds ratio (OR) being 1.58 (95% CI 1.24-2.00). Similarly, compared with Arg194Arg (CC) wild-type genotype, elevated risks were associated with the Trp194Trp (TT) for carcinoma (ORs and 95% CIs being 2.09 [1.45-3.02]) but not for heterozygote Arg194Trp (CT). In addition, three common haplotypes were found to be associated with an increased risk of cervical carcinoma. Using 194Arg-280Arg-399Arg as the reference, the OR and 95% confidence interval for 194Arg-280Arg-399Gln, 194Arg-280His-399Arg, 194Trp-280Arg-399Arg were 2.30 (1.86-2.85), 1.85 (1.41-2.41), 1.98 (1.62-2.40), respectively. The significantly increased risk associated with the haplotypes was also observed in squamous cell carcinoma (SCC) for all three common haplotypes using 194Arg-280Arg-399Arg as the reference. Neither difference was found for adenocarcinoma and CIN. All three SNPs and haplotypes did not confer more risk of high-risk human papillomavirus infection in carcinoma, CIN, and normal subgroup. Our findings suggest that XRCC1 polymorphisms including genotypes and haplotypes contribute to susceptibility to the development of cervical SCC, and the increased susceptibility is probably not through increasing susceptibility to human papillomavirus infection.

摘要

为评估X射线修复交叉互补基因1(XRCC1)单核苷酸多态性(SNP)对宫颈癌风险的影响,我们开展了一项病例对照研究,纳入1012例患者,其中包括539例宫颈癌患者、473例宫颈上皮内瘤变(CIN)患者以及800名正常女性对照,并对3个XRCC1 SNP(Arg194Trp、Arg280His和Arg399Gln)进行基因分型。我们发现,与携带Arg399Gln(GG)基因型的个体相比,携带纯合Gln399Gln(AA)基因型的个体患宫颈癌的风险显著增加2.32倍(95%可信区间为1.47 - 3.65),杂合子Arg399Gln(GA)基因型也与宫颈癌风险显著增加相关,校正比值比(OR)为1.58(95%可信区间为1.24 - 2.00)。同样,与Arg194Arg(CC)野生型基因型相比,Trp194Trp(TT)基因型与宫颈癌风险升高相关(OR及95%可信区间为2.09 [1.45 - 3.02]),但杂合子Arg194Trp(CT)基因型则不然。此外,发现3种常见单倍型与宫颈癌风险增加相关。以194Arg - 280Arg - 399Arg为参照,194Arg - 280Arg - 399Gln、194Arg - 280His - 399Arg、194Trp - 280Arg - 399Arg的OR及95%可信区间分别为2.30(1.86 - 2.85)、1.85(1.41 - 2.41)、1.98(1.62 - 2.40)。以194Arg - 280Arg - 399Arg为参照,在所有3种常见单倍型的鳞状细胞癌(SCC)中也观察到与单倍型相关的风险显著增加。腺癌和CIN未发现差异。在宫颈癌、CIN和正常亚组中,所有3个SNP和单倍型均未增加高危人乳头瘤病毒感染风险。我们的研究结果表明,包括基因型和单倍型在内的XRCC1多态性与宫颈SCC发生的易感性有关,且易感性增加可能并非通过增加人乳头瘤病毒感染易感性实现。

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