Chen Wen, Wang Qin, Liu Mang, Ding Xiao-bing
Shanghai Xujiahui Community Medical Service Center, Shanghai, 200030, China.
Tumour Biol. 2014 Apr;35(4):3597-603. doi: 10.1007/s13277-013-1474-8. Epub 2013 Dec 6.
Many studies have examined the association between APE1 Asp148Glu (rs3136820) polymorphism gene polymorphisms and lung cancer risk in various populations, but their results have been inconsistent. To assess this relationship more precisely, a meta-analysis was performed. PubMed and CNKI databases were searched for case-control studies published up to October 2013. Data were extracted, and pooled odds ratios (OR) with 95% confidence intervals (CI) were calculated. Ultimately, 14 studies, comprising 4,165 lung cancer cases and 5,438 controls were included. Overall, for Glu carriers (Asp/Glu + Glu/Glu) versus wild-type homozygotes (Asp/Asp), the pooled OR was 1.05 (95% CI = 0.96-1.15 P = 0.000 for heterogeneity); for Glu/Glu versus Asp/Asp, the pooled OR was 1.07 (95% CI = 0.95-1.21 P = 0.007 for heterogeneity). In the stratified analysis by ethnicity, the significantly risks were not found among Asians or Caucasians. This updated meta-analysis suggests that the APE1 Asp148Glu polymorphisms are not associated with lung cancer risk among Asians or Caucasians.
许多研究探讨了APE1基因Asp148Glu(rs3136820)多态性与不同人群肺癌风险之间的关联,但其结果并不一致。为更精确地评估这种关系,进行了一项荟萃分析。检索了PubMed和中国知网数据库中截至2013年10月发表的病例对照研究。提取数据并计算合并比值比(OR)及95%置信区间(CI)。最终纳入了14项研究,包括4165例肺癌病例和5438例对照。总体而言,对于Glu携带者(Asp/Glu + Glu/Glu)与野生型纯合子(Asp/Asp),合并OR为1.05(95%CI = 0.96 - 1.15,异质性P = 0.000);对于Glu/Glu与Asp/Asp,合并OR为1.07(95%CI = 0.95 - 1.21,异质性P = 0.007)。在按种族进行的分层分析中,未在亚洲人或高加索人中发现显著风险。这项更新的荟萃分析表明,APE1 Asp148Glu多态性与亚洲人或高加索人的肺癌风险无关。