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张文娟, 吴逸明, 吴拥军. DNA修复基因XRCC1多态与肺癌易感性[J]. 中国公共卫生, 2005, 21(5): 561-563.
引用本文: 张文娟, 吴逸明, 吴拥军. DNA修复基因XRCC1多态与肺癌易感性[J]. 中国公共卫生, 2005, 21(5): 561-563.
ZHANG Wenjuan, WU Yiming, WU Yongjun.. Study on polymorphism of XRCC1 and susceptibility to lung cancer[J]. Chinese Journal of Public Health, 2005, 21(5): 561-563.
Citation: ZHANG Wenjuan, WU Yiming, WU Yongjun.. Study on polymorphism of XRCC1 and susceptibility to lung cancer[J]. Chinese Journal of Public Health, 2005, 21(5): 561-563.

DNA修复基因XRCC1多态与肺癌易感性

Study on polymorphism of XRCC1 and susceptibility to lung cancer

  • 摘要:
      目的   研究碱基切除修复基因XRCC1单核苷酸多态及与吸烟交互作用对肺癌易感性的影响。
      方法   以病例-对照研究的方法, 采用PCR扩增限制性酶切法(PCR-RFLP)检测肺癌病例(n=149)和按性别、年龄频数匹配的正常对照者(n=157)XRCC1基因C25 304T和G28152A多态, 并比较不同基因型与肺癌风险的关系及基因多态与吸烟之间的交互作用对肺癌风险的影响。
      结果   肺癌患者中, XRCC12 6304TT变异基因型频率为12.8%, 高于对照组6.4%(P < 0.05);此种基因型个体发生肺癌的风险是其他基因型的2.0倍(调整OR=1.6, 95%CI=0.57~4.47)。2812 5AA基因型频率在病例组中为10.7%, 高于对照组8.3%(P < 0.05);经性别、年龄和吸烟状况调整, 此基因个体发生肺癌的风险是其他基因型的2.1倍(95%CI=0.73~6.15)。XRCC1基因这两个多态位点之间没有明显的联合作用, 但基因型均吸烟之有联合作用而增高肺癌风险。
      结论   XRCC1基因多态及其与吸烟的交互作用在肺癌的发生过程中起一定作用。

     

    Abstract:
      Objective   To evaluate the correlation of the single nucleotide polymorphism of XRCC1 and smoking, independently and in combination with the risk of lung cancer.
      Methods   A case-control study of 149 lung cancer patients and 157 control subjects(matched for age, sex)was conducted to investigate the role of XRCC1 gene in lung cancer.Genotyping was performed using PCR based restriction fragment length polymorhphism techniques.The adjusted odds ratio(OR)and 95% confidence interval(CI)was calculated using multivariate logistic regressing.
      Results   The frequency of TTallele in case group(12.8%)was significantly higher than that in control group(6.4%), with the OR for lung cancer being 2.0(adjusted OR=116, 95%CI 0.57-4.47).The frequency of AA allele in case group(10.7%)was significantly higher than that in control group(8.3%), with the adjusted OR for lung cancer being 2.1(95%CI 0.73-6.15).Further more, the risk of lung cancer for XRCC1 genety pes appeared to be pronounced compared with nonsmokers.But no inter action was found between two either genetype.
      Conclusion   These findings support the hypot hesis which the polymorphsm of XRCC1 and its correlation with smoking do contribute to the risk of developing lung cancer.

     

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