He M G, Zheng K, Tan D, Wang Z X
Department of Hepatobiliary Surgery, Nuclear Industry 215 Hospital of Shaanxi Province, Xianyang, China.
Genet Mol Res. 2016 Mar 31;15(1):gmr7879. doi: 10.4238/gmr.15017879.
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.
我们开展了一项研究,以调查中国人群中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月期间,从陕西省核工业215医院招募了217例胰腺癌患者和244例对照受试者。按照制造商的说明,使用天根血液DNA提取试剂盒(中国北京天根生化科技有限公司)从外周血样本中提取基因组DNA。通过聚合酶链反应-限制性片段长度多态性对ERCC1 rs3212986和ERCC2 rs13181多态性进行基因分型。无条件逻辑回归分析显示,与AA基因型受试者相比,ERCC1 rs3212986的CC基因型受试者易患胰腺癌(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。然而,在共显性、显性和隐性模型中,ERCC2 rs13181多态性与胰腺癌风险之间未发现显著差异。我们认为,尽管需要进一步研究来证实我们的发现,但在共显性、显性和隐性模型中,ERCC1 rs3212986多态性增加了患胰腺癌的易感性。