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作 者:范祖鹏[1] 彭群新[2] 高歌[1] 吴文婷[1] 钱吉[1] 陈红岩[1]
机构地区:[1]复旦大学生命科学学院遗传工程国家重点实验室,上海200433 [2]苏州大学第一附属医院检验科,苏州215006
出 处:《癌变.畸变.突变》2010年第4期265-270,共6页Carcinogenesis,Teratogenesis & Mutagenesis
基 金:上海市科委重大项目(09JC1402200;06DZ19501);上海市公共卫生优秀学科带头人培养计划(08GWD07);国家自然科学基金青年基金(30800622)
摘 要:目的:探讨人类DNA聚合酶ε基因POLE1单核苷酸多态性(SNP)与肺癌易感性间的关系。方法:采用病例对照研究方法,选择经组织学确诊的肺癌患者462例,以及相同地区,性别年龄频数匹配的对照466例,针对经筛选的5个SNP进行基因型检测,通过统计分析研究基因频率与肺癌风险的关系,并探讨吸烟在其中的影响。结果:病例组rs5744738基因频率分布高于对照组(P<0.05)。A/A纯合变异携带人群的患肺癌风险显著降低(校正OR=0.47,95%CI:0.25~0.91)。在分层分析中,60岁以上人群患肺癌的风险显著下降(校正OR=0.28,95%CI:0.09~0.91),无患肿瘤家族史人群下降到0.42倍(校正OR=0.42,95%CI:0.19~0.90)。随着吸烟量的增加,G/G或G/A基因型人群肺癌风险显著升高。rs5744962变异位点(T→C)可提高非吸烟人群的患肺癌风险至1.75倍(95%CI:1.02~3.00)。结论:选取的5个人类POLE1基因SNP的多态性可能与中国汉族人群肺癌遗传易感性有关,在携带rs5744738及与之紧密连锁的rs4883545、rs5744873突变纯合基因的人群,患肺癌的风险显著降低,而携带rs5744962、rs5745047突变基因位点的非吸烟人群患肺癌的风险升高。OBJECTIVE:To assess the association between the POLE1 SNPs and lung cancer susceptibility.METHODS:The genotypes and allele frequencies of 5 SNPs(rs5745047,rs5744962,rs5744873,rs5744738,rs4883545)of POLE1 gene were calculated and analyzed in 462 histologically confirmed lung cancer cases and 466 cancer-free controls in a Chinese Han population.RESULTS:People with rs5744738 A/A genotype had a decreased lung cancer risk of 0.47 times(95%CI:0.25-0.91),0.28 times in the age group of over 60(95%CI:0.09-0.91),and 0.42 times in non-family cancer history group(95%CI:0.19-0.90).The joint effect analysis showed that G/G or G/A carriers had a significant rise in lung cancer risk with increasing smoking.The rs5744962 C allele non-smoking carriers had an 1.75 folds lung cancer risk(95%CI:1.02-3.00).CONCLUSION:The population with homologous mutations of rs5744738,rs4883545 and rs5744873 showed significant decline in lung cancer risk,while the non-smoking carriers of rs5744962 and rs5745047 mutation allele had an increased lung cancer risk.
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