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DNA修复基因XRCC1多态性与肺癌易感性的关系 被引量:2

Relationship between polymorphisms of DNA repair gene XRCC1 and susceptibility to lung cancer
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摘要 目的:研究碱基切除修复基因XRCC1多态性与肺癌易感性的关系。方法:采用病例-对照研究,收集太原市原发性肺癌患者111例为病例组,同时随机抽取210名健康居民作为对照组,并进行流行病学调查。应用PCR-RFLP方法分析由内切酶MspI识别XRCC1基因Arg399Gln位点的多态性,比较不同基因型与肺癌易感性的关系,以及基因多态性与吸烟之间对肺癌易感性的交互作用。结果:XRCC1密码子399杂合基因型Arg/Gln可能对鳞癌有较弱的保护效应,并可能降低吸烟者患肺癌的危险性。而纯合突变基因型Gln/Gln与和吸烟的存在协同作用可显著提高肺癌的危险度。结论:碱基切除修复基因XRCC1密码子399的多态性可能会对肺癌易感性产生影响,并可能与吸烟量之间存在一定的协同作用。 Purpose: The current study analyzed the polymorphisms of DNA repair gene XRCC1 and relationship hetween genetic variations and susceptibility to lung eancer Methods:A ease-control study of 111 patients with lung cancer and 210 normal residents as controls was conducted to deteet XRCC1 polymorphisms at Arg399Gln loci.Genotypes were analyzed by PCR-based restrietion fragment length polymorphism(RLFP)techniques.Results:XRCC1 codon 399 heterozygous genotype Arg/Gln might have weaker protection effect on squamous cell careinoma and reduce the risk of lung eancer on smokers.Homozygous genotype Gln/Gln of XRCC1 codon 399 might increase the risk of lung cancer and have synergismight contribute to the susceptibility to lung cancer and have synergitie with smoking.Conclusion:The results demonstrated that genetic polymorphism of XRCC1 DNA repair gene might contrilbute to the susceptibility to lung cancer and have synergistic effect with somking.
出处 《中国癌症杂志》 CAS CSCD 2005年第4期335-338,共4页 China Oncology
关键词 XRCC1基因 基因多态性 肺癌易感性 XRCC1 gene Genetic polymorphism susceptibility to lung cancer
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  • 1Kubota Y, Nash RA , Klungland A , et al. Reconstitution of DNA base excision repair with purified human proteins:interaction between DNA polymerase beta and the XRCCI protein[J] . EMBO J, 1996,15 ( 23 ) :6662-6670.
  • 2Wilson SH. Mammalian base excision repair and DNA poly - merase beta[J]. Mutat Res,1998,407(3) :203-215.
  • 3Cappelli E , Taylor M , Cevaseo A , et al. Involvement of XRCC1 and DNA ligase 111 gene producls in DNA base excision repair[J]. J Biol Chem, 1997,272( 38 ) :23970-23975.
  • 4D' Silva ID , Pelletier JD , Lagueux J , et al. Relative affinities ofpoly (ADP-ribose) polymerase and DNA-dependent protein kinase for DNA strand interruptions [J]. Biochim Biophys Avta,1999,1430( 1 ) :119-126.
  • 5Shen MR, Jones IM, Mohrenweiser H. Nonconservative amino acid substitution variants exist at polymorphic frequency in DNA repair genes in healthy humans [ J ]. Cancer Res, 1998,58 ( 4 ) :604-608.
  • 6Abdel-Rahman SZ, EI-Zein RA. The 399Gln polymorphism in the DNA repair gene XRCCI modulates lhe genotoxic response induced in human lymphocytes by the tobacco-specific nitrosamine NNK[J ] . Carvcer Lett,2000,159( 1 ) :63-71.
  • 7Lunn R, Langlois RG, Hsieh LL,et al. XRCCI polymorphisms: effects on aflatoxin B1-DNA adducts and glycophorin A variant frequency[ J]. Cancer Res, 1999,59( 11 ) :2557-2561.
  • 8Thompson LH, Brookman KW, Jones N J, et al. Molecular cloning of the human XRCCI gene, which corrects defective DNA strand-break repair and sister chromatid exchange [ J ]. Mol Cell Biol, 1990,10(12) :6160-6171.
  • 9Hompson LH, West MG. XRCCI keeps DNA from getting stranded[J]. Murat Res,2000,459( 1 ) :1-18.
  • 10Beckman KB, Ames BN. Oxidative decay of DNA [ J]. J Biol Chem, 1997,272 ( 32 ) : 19633-19636.

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