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作 者:蒋雯[1] 王美林[2] 张治中[2] 陈小军[2] 朱慧[2] 钱年风[2] 傅士龙[1] 张正东[2] 韩素萍[1]
机构地区:[1]南京医科大学第一附属医院妇产科,江苏南京210029 [2]南京医科大学公共卫生学院,江苏南京210029
出 处:《南京医科大学学报(自然科学版)》2009年第1期1-6,共6页Journal of Nanjing Medical University(Natural Sciences)
基 金:国家自然科学基金资助(30872084);江苏省省属高校自然科学重大基础研究项目(08KJA330001);教育部生殖医学重点实验室开放基金
摘 要:目的:探讨XRCC1基因多态性与江苏人群宫颈癌易感性之间的关系。方法:采用基于医院的分子流行病学病例对照研究方法,选取436例经组织病理学确诊为宫颈癌的新发患者作为病例组和503例年龄(±5岁)、性别相匹配的非肿瘤者作为对照组;采用聚合酶链反应限制性片段长度多态性(PCR-RFLP)方法对XRCC1启动子区-77T>C和外显子10区的Arg399Glu基因多态性进行基因分型,比较不同基因型携带者患宫颈癌的危险性;通过分层分析探讨初潮年龄、患者年龄及产次对罹患宫颈癌的影响。结果:与XRCC1-77TT相比,-77TC/CC基因型可减少罹患宫颈癌的危险性(OR=0.64,95%CI=0.48~0.86)。携带3~4个危险等位基因者比携带1~2个等位基因者患宫颈癌的危险性更大(OR=1.44,95%CI=1.01~2.04)。分层分析结果显示,年龄较大和产次较多且携带3~4个危险等位基因者罹患宫颈癌的危险性分别增加1.64倍(95%CI=1.02~2.64)和1.66倍(95%CI=1.01~2.72)。本研究未发现XRCC1Arg399Glu多态性与宫颈癌之间存在显著性相关。结论:XRCC1基因启动子-77T>C多态性显著降低江苏地区汉族人群罹患宫颈癌的危险性。Objective:To explore the association of XRCC1 gene single nucleotide polymorphisms and the risk of cervical cancer. Methods:In a hospital-based case-control study of 436 patients with newly, diagnosed cervical carcinoma and 503 cancer-free controls frequency-matched by age(±5 years), we genotyped the -77T〉C and Arg399Glu polymorphisms of XRCC1 gene by the poly-rnerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) method. We further analyzed the interaction of age, menarche age, and parity. Results: We found that the -77T〉C variant genotypes were associated with significantly decreased risk of cervical cancer adjusted odds ratio(OR) = 0.64; 95% confidence interval(CI)=0.48-0.86, compared with the wild-type homozygote. Moreover, individuals with 3-4 risk alleles increased the risk of cervical cancer accompanied with older age( 〉 50 years)(OR=1.64, 95%CI=1.02-2.64) and parity (OR=1.66,95%CI=1.01-2.72). By contrast, no significant association was observed between the Arg399Gln polymorphism and cervical cancer risk. Conclusion:Our finding indicated that the XRCC1-77 CC/CT genotype was significantly associated with a decreased risk of cervical cancer in Jiangsu population.
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