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首页> 外文期刊>Tumour biology : >Association of single nucleotide polymorphisms of nucleotide excision repair genes with laryngeal cancer risk and interaction with cigarette smoking and alcohol drinking.
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Association of single nucleotide polymorphisms of nucleotide excision repair genes with laryngeal cancer risk and interaction with cigarette smoking and alcohol drinking.

机译:核苷酸切除修复基因的单核苷酸多态性与喉癌风险以及与吸烟和饮酒的相互作用的关联。

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摘要

We investigated the potential association of 12 single nucleotide polymorphisms (SNPs) of nucleotide excision repair (NER) genes with risk of laryngeal cancer. A ratio of 1:1 matched case-control study was conducted. Conditional regression analysis indicated that subjects with ERCC1 rs11615 CC and C allele had an increased risk of laryngeal cancer compared with the TT genotype. Individuals with the ERCC5 rs17655 GG and G allele had a moderately increased risk of laryngeal cancer when compared with the CC genotype. By stratified analysis, ERCC1 rs11615 CC genotype and C allele were significantly associated with greatly increased risk of laryngeal cancer in ever smokers. ERCC1 rs11615 and ERCC5 rs17655 polymorphisms were associated with a moderately increased risk of this cancer in ever drinkers. In summary, we suggest that genetic variations in ERCC1 rs11615 and ERCC5 rs17655 are associated with laryngeal cancer risk in a Chinese population, especially in ever smokers and drinkers. Our finding could be helpful in identifying people at high risk for the disease for early intervention.
机译:我们调查了核苷酸切除修复(NER)基因的12个单核苷酸多态性(SNP)与喉癌风险之间的潜在关联。进行了1:1的匹配病例对照研究。条件回归分析表明,与TT基因型相比,ERCC1 rs11615 CC和C等位基因的受试者发生喉癌的风险增加。与CC基因型相比,ERCC5 rs17655 GG和G等位基因个体的喉癌风险有所增加。通过分层分析,ERCC1 rs11615 CC基因型和C等位基因与吸烟者的喉癌风险显着相关。 ERCC1 rs11615和ERCC5 rs17655多态性与饮酒者罹患该癌症的风险适度增加有关。总而言之,我们建议ERCC1 rs11615和ERCC5 rs17655的遗传变异与中国人群尤其是吸烟者和饮酒者的喉癌风险有关。我们的发现可能有助于识别出患有该疾病高风险的人,以便进行早期干预。

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