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中国人群中XRCC1基因多态性与胰腺癌风险的关联

Association of XRCC1 gene polymorphisms and pancreatic cancer risk in a Chinese population.

作者信息

Wang L J, Wang H T, Wang X X

机构信息

Department of Hepatobiliary Surgery, Yantai Affiliated Hospital of Binzhou Medical University, Yantai, China.

Gastrointestinal Surgery Department I, Yantai Yuhuangding Hospital, Yantai, China.

出版信息

Genet Mol Res. 2016 Jun 3;15(2):gmr8080. doi: 10.4238/gmr.15028080.

Abstract

We conducted a case-control study to assess the role of the XRCC1 Arg399Gln, Arg280His, and Arg194Trp gene polymorphisms in pancreatic cancer susceptibility in a Chinese population. A total of 152 patients diagnosed with pancreatic cancer and 264 control subjects were enrolled in this study between March 2012 and October 2014. XRCC1 Arg399Gln, Arg280His, and Arg194Trp were genotyped using the polymerase chain reaction-restriction fragment length polymorphism method. As determined by the chi-squared test, a statistically significant difference was observed between pancreatic cancer patients and control subjects in regard to the genetic distribution of XRCC1 Arg399Gln (χ(2) = 16.13, P < 0.001). Using an unconditional regression analysis, we found that the TT genotype of Arg399Gln was associated with a significantly increased risk of pancreatic cancer (OR = 2.33, 95%CI = 1.20-4.51), and that the CT+TT genotype also significantly increased pancreatic cancer risk (OR = 1.58, 95%CI = 1.04-2.41), compared to the wild-type genotype. In conclusion, we found that XRCC1 Arg399Gln genetic variations are associated with pancreatic cancer development, whereas the XRCC1 Arg280His and Arg194Trp polymorphisms did not affect pancreatic cancer risk.

摘要

我们开展了一项病例对照研究,以评估XRCC1基因的Arg399Gln、Arg280His和Arg194Trp基因多态性在中国人群胰腺癌易感性中的作用。2012年3月至2014年10月期间,共有152例诊断为胰腺癌的患者和264例对照者纳入本研究。采用聚合酶链反应-限制性片段长度多态性方法对XRCC1基因的Arg399Gln、Arg280His和Arg194Trp进行基因分型。经卡方检验确定,在XRCC1基因Arg399Gln的基因分布方面,胰腺癌患者与对照者之间存在统计学显著差异(χ(2)=16.13,P<0.001)。通过无条件回归分析,我们发现,与野生型基因型相比,Arg399Gln的TT基因型与胰腺癌风险显著增加相关(OR=2.33,95%CI=1.20-4.51),CT+TT基因型也显著增加胰腺癌风险(OR=1.58,95%CI=1.04-2.41)。总之,我们发现XRCC1基因Arg399Gln的基因变异与胰腺癌发生相关,而XRCC1基因Arg280His和Arg194Trp多态性不影响胰腺癌风险。

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