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Polymorphisms in nucleotide excision repair genes and risk of primary prostate cancer in Chinese Han populations

机译:中国汉族人群核苷酸切除修复基因的多态性与原发性前列腺癌的风险

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摘要

Genetic variants of nucleotide excision repair (NER) genes have been extensively investigated for their roles in the development of prostate cancer (PCa); however, the published results have been inconsistent. In a hospital-based case-control study of 1,004 PCa cases and 1,055 cancer-free controls, we genotyped eight potentially functional single nucleotide polymorphisms (SNPs) of NER genes (i.e., XPC, rs2228001 T>G and rs1870134 G>C; XPD, rs13181 T>G and rs238406 G>T; XPG, rs1047768 T>C, rs751402 C>T, and rs17655 G>C; and XPF, rs2276464 G>C) and assessed their associations with risk of PCa by using logistic regression analysis. Among these eight SNPs investigated, only XPC rs1870134 CG/CC variant genotypes were associated with a decreased risk of prostate cancer under a dominant genetic model (adjusted odds ratio [OR] = 0.77, 95% confidence interval [CI] = 0.64–1.91, P = 0.003). Phenotype-genotype analysis also suggested that the XPC rs1870134 CG/CC variant genotypes were associated with significantly decreased expression levels of XPC mRNA in a mix population of different ethnicities. These findings suggested that XPC SNPs may contribute to risk of PCa in Eastern Chinese men.
机译:已经广泛研究了核苷酸切除修复(NER)基因的遗传变异在前列腺癌(PCa)发生中的作用。但是,已发布的结果不一致。在一项基于医院的病例对照研究中,对1,004个PCa病例和1,055个无癌对照进行了基因分型,我们对NER基因的8个潜在功能性单核苷酸多态性(SNP)进行了基因分型(即XPC,rs2228001 T> G和rs1870134 G> C; XPD ,rs13181 T> G和rs238406 G> T; XPG,rs1047768 T> C,rs751402 C> T和rs17655 G> C;以及XPF,rs2276464 G> C),并通过逻辑回归分析评估了它们与PCa风险的关系。在这八个被调查的SNP中,只有XPC rs1870134 CG / CC变异基因型与显性遗传模型下的前列腺癌风险降低相关(校正比值比[OR] = 0.77,95%置信区间[CI] = 0.64–1.91, P = 0.003)。表型-基因型分析还表明,XPC rs1870134 CG / CC变异基因型与不同种族混合人群中XPC mRNA的表达水平显着降低有关。这些发现表明,XPC SNP可能会导致中国东部男性患PCa的风险。

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