Du Liang, Liu Yuqi, Xue Pei, Song Chenxi, Shen Jiani, He Qing, Peng Yuanling, Tong Xiang, Tang Lizhi, Zhang Yonggang
The Periodical Press of West China Hospital, Sichuan University, Guoxuexiang 37, Chengdu, Sichuan, 610041, China.
Tumour Biol. 2015 Jun;36(6):4545-54. doi: 10.1007/s13277-015-3099-6. Epub 2015 Jan 27.
The associations between the Arg399Gln polymorphism in X-ray repair cross-complementing gene 1 (XRCC1) gene and the risk of hematological malignancies have been extensively investigated. However, the results were inconsistent. The objective of the current study is to investigate the association by meta-analysis. We searched PubMed database, Embase database, CNKI database, Wanfang database, and Weipu database, covering all studies until August 7, 2013. Statistical analysis was performed by using the Revman4.2 software and the Stata10.0 software. A total of 27 case-control studies concerning the Arg399Gln polymorphism were included from 26 articles. The results suggested that the Arg399Gln polymorphism was not associated with an increased/decreased risk of hematological malignancies in total analysis (OR = 1.15, 95 % confidence interval (CI) = 0.97-1.35, P = 0.10 for Arg/Gln + Gln/Gln vs. Arg/Arg). In the subgroup analysis by ethnicity and cancer types, significant association was found in Asians (OR = 1.35, 95 % CI = 1.04-1.75, P = 0.03) but not in Europeans (OR = 1.07, 95 % CI = 0.86-1.33, P = 0.56), and in leukemia (OR = 1.25, 95 % CI = 1.02-1.54, P = 0.03) but not in lymphoma (OR = 0.98, 95 % CI = 0.80-1.20, P = 0.84) or myeloma (OR = 1.13, 95 % CI = 0.23-5.69, P = 0.88). The current meta-analysis indicated that the Arg399Gln polymorphism in the XRCC1 gene might be a risk factor for hematological malignancies in Asians or for leukemia. In future, more large-scale case-control studies are needed to validate these results.
X射线修复交叉互补基因1(XRCC1)基因中的Arg399Gln多态性与血液系统恶性肿瘤风险之间的关联已得到广泛研究。然而,结果并不一致。本研究的目的是通过荟萃分析来探究这种关联。我们检索了PubMed数据库、Embase数据库、中国知网数据库、万方数据库和维普数据库,涵盖截至2013年8月7日的所有研究。使用Revman4.2软件和Stata10.0软件进行统计分析。从26篇文章中纳入了27项关于Arg399Gln多态性的病例对照研究。结果表明,在总体分析中,Arg399Gln多态性与血液系统恶性肿瘤风险的增加/降低无关(Arg/Gln + Gln/Gln与Arg/Arg相比,OR = 1.15,95%置信区间(CI)= 0.97 - 1.35,P = 0.10)。在按种族和癌症类型进行的亚组分析中,在亚洲人中发现了显著关联(OR = 1.35,95% CI = 1.04 - 1.75,P = 0.03),而在欧洲人中未发现(OR = 1.07,95% CI = 0.86 - 1.33,P = 0.56);在白血病中发现了显著关联(OR = 1.25,95% CI = 1.02 - 1.54,P = 0.03),而在淋巴瘤中未发现(OR = 0.98,95% CI = 0.80 - 1.20,P = 0.84)或在骨髓瘤中未发现(OR = 1.13,95% CI = 0.23 - 5.69,P = 0.88)。当前的荟萃分析表明,XRCC1基因中的Arg399Gln多态性可能是亚洲人患血液系统恶性肿瘤或患白血病的一个风险因素。未来,需要更多大规模的病例对照研究来验证这些结果。