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Association between ERCC1 and ERCC2 gene polymorphisms and susceptibility to pancreatic cancer

机译:ERCC1和ERCC2基因多态性与胰腺癌易感性的关系

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We conducted a study to investigate the association between ERCC1 (rs3212986) and ERCC2 (rs13181) gene polymorphisms and the risk of pancreatic cancer in a Chinese population. A total of 217 pancreatic cancer patients and 244 control subjects were recruited from the Nuclear Industry 215 Hospital of Shaanxi Province between February 2013 and December 2014. Genomic DNA was extracted from peripheral blood samples using a TIANamp Blood DNA Kit (Tiangen, Beijing, China) according to the manufacturer’s instructions. The ERCC1 rs3212986 and ERCC2 rs13181 polymorphisms were genotyped by polymerase chain reaction-restriction fragment length of polymorphism. Unconditional logistic regression analyses showed that subjects with the CC genotype of ERCC1 rs3212986 were susceptible to the development of pancreatic cancer when compared with subjects with the AA genotype (OR = 2.57, 95%CI = 1.34-5.02). The ERCC1 rs3212986 gene polymorphism was associated with increased risk of pancreatic cancer in the dominant (OR = 1.54, 95%CI = 1.05-2.28) and recessive (OR = 2.22, 95%CI = 1.20-4.19) models. However, no significant difference was found between the ERCC2 rs13181 polymorphism and the risk of pancreatic cancer in the codominant, dominant, and recessive models. We suggest that the ERCC1 rs3212986 polymorphism increases susceptibility to pancreatic cancer in the codominant, dominant, and recessive models, although further studies are needed to confirm our findings.
机译:我们进行了一项研究,以调查中国人口中ERCC1(rs3212986)和ERCC2(rs13181)基因多态性与胰腺癌风险之间的关联。 2013年2月至2014年12月,共从陕西省核工业215医院招募了217位胰腺癌患者和244位对照对象。使用TIANamp血液DNA试剂盒(天健,北京)从外周血样本中提取基因组DNA。根据制造商的说明。 ERCC1 rs3212986和ERCC2 rs13181多态性通过聚合酶链反应-多态性的限制性片段长度进行基因分型。无条件逻辑回归分析显示,与具有AA基因型的受试者相比,具有ERCC1 rs3212986 CC基因型的受试者更容易发生胰腺癌(OR = 2.57,95%CI = 1.34-5.02)。在显性(OR = 1.54,95%CI = 1.05-2.28)和隐性(OR = 2.22,95%CI = 1.20-4.19)模型中,ERCC1 rs3212986基因多态性与胰腺癌风险增加相关。但是,在显性,显性和隐性模型中,ERCC2 rs13181多态性与胰腺癌风险之间没有发现显着差异。我们建议ERCC1 rs3212986基因多态性增加在显性,显性和隐性模型中对胰腺癌的易感性,尽管还需要进一步的研究来证实我们的发现。

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