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作 者:范雪娇[1] 任朋亮[1] 卢钟娇[1] 赵书[1] 杨晓龙[1] 刘戟[1]
机构地区:[1]四川大学华西基础医学与法医学院生物化学与分子生物学教研室,成都610041
出 处:《四川大学学报(医学版)》2013年第4期568-572,共5页Journal of Sichuan University(Medical Sciences)
基 金:教育部博士点基金新教师项目(No.20070610124);教育部留学回国人员启动基金项目(No.2008890-19-11)资助
摘 要:目的探究DNA双链断裂修复基因XRCC4、RAD51单核苷酸多态性与食管癌易感性的关系。方法采用以医院为基础的病例-对照研究方法,应用PCR限制性内切酶片段长度多态性(PCR-RFLP)检测包括正常对照61例,食管癌患者123例XRCC4基因启动子区G-1394T(rs6869366)位点,以及RAD51-G135C位点的单核苷酸多态性。通过logistic回归分析计算出比值比(OR)和95%置信区间(95%CI)。结果 XRCC4rs6869366位点G等位基因的基因型(GT+GG)的携带者患食管癌的风险显著增加(OR=3.022,95%CI=1.487~6.142,P=0.002)。RAD51基因型GC和CC与携带GG的野生型个体相比,携带RAD51变异基因型(GC和CC)的个体具有更高的患癌风险(OR=3.643,95%CI=1.501~8.842,P<0.05)。结论 DNA损伤修复系统中的基因多态性很可能与食管癌发生的易感性有关,XRCC4G-1394T,RAD51-G135C位点多态性改变均可增加食管癌的发病风险。Objective Investigate the association between genetic polymorphism of DSBs repair gene XRCC4, RAD51 and susceptibility to esophageal cancer (EC). Methods A hospital based case-control study with 123 EC cases and 61 controls in a Chinese population was conducted. PCR-RFLP was applied to investigate the genotype of XRCC4 promoter G-1394T (rs6869366) and RAD51-G135C and then statistical analysis was conducted by calculating the adjusted odds ratios (OR) and 95% confidence intervals (95%CI). Results A significant difference of XRCC4-1394 polymorphism was observed between EC cases and controls (P〈0.05). Carriers of the XRCC4 rs6869366 G allele (GCq-GG) were at a higher risk of developing EC with the TT genotype as reference (OR= 3. 022, 95%CI= 1. 487-6. 142, P= 0. 002). When GG served as the reference group of RAD51-G135C allele, variant genotype (GC and CC) had a significant increased risk of lung cancer (OR=3. 643,95 %CI= 1. 501-8. 842, P〈0.05). Conclusion Our findings indicated that genetic variants in DNA repair pathways may be involved in esophageal tumorigenesis. XRCC4 G-1394T and RAD51-G135C conferred risk for the process of developing EC.
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