Liu Jun, Cao Xiao-Lin, Zhang Zhen, Lei Da-Peng, Jin Tong, Yu Xue-Min, Pan Xin-Liang
Department of Otolaryngology, Qilu Hospital, Shandong University, Jinan, China.
Asian Pac J Cancer Prev. 2011;12(10):2491-4.
Several research groups have investigated the influence of the human 8-oxoguanine DNA glycosylase 1 (hOGG1) Ser326Cys polymorphism on head and neck cancer (HNC) susceptibility. However, the results remain inconclusive and controversial. We therefore conducted the present meta-analysis.
Relevant studies were identified through a search of PubMed databases until July 2011 and selected on the basis of established inclusion criteria for publications.
A total of 8 case-control studies on the association of hOGG1 Ser326Cys polymorphism with HNC risk were included in the present meta-analysis. Overall significant associations were observed (G allele vs. C allele: OR=1.49, 95%CI=1.08-2.05, P<0.01 for heterogeneity; GG vs.CC: OR=2.30, 95%CI=1.05-5.05, P<0.01 for heterogeneity; CG vs. CC: OR=1.40, 95%CI=1.03-1.90, P<0.01 for heterogeneity; dominant model (GG+CG vs. CC): OR=1.52, 95%CI=1.06-2.16, P<0.01 for heterogeneity; recessive model (GG vs. CG+CC): OR=2.04, 95%CI=1.05-3.96, P=0.01 for heterogeneity) after excluding the studies that were not in agreement with HWE. On performance of a subgroup meta-analysis by ethnicity, significant associations were found (G allele vs. C allele: OR=1.40, 95%CI=1.001-1.95, P<0.01 for heterogeneity; GG vs.CC: OR=2.30, 95%CI=1.05-5.05, P<0.01 for heterogeneity; recessive model (GG vs. CG+CC): OR=2.04, 95%CI=1.05-3.96, P=0.01 for heterogeneity) in Caucasian populations after excluding one study not in agreement with HWE.
Our results suggested that the G allele might be associated with an increased risk of HNC in Caucasian populations.
多个研究小组已对人类8-氧代鸟嘌呤DNA糖基化酶1(hOGG1)Ser326Cys多态性对头颈部癌(HNC)易感性的影响进行了研究。然而,结果仍不明确且存在争议。因此,我们进行了本次荟萃分析。
通过检索PubMed数据库直至2011年7月来确定相关研究,并根据既定的纳入标准选择发表的文献。
本次荟萃分析共纳入了8项关于hOGG1 Ser326Cys多态性与HNC风险关联的病例对照研究。排除不符合哈迪-温伯格平衡(HWE)的研究后,观察到总体存在显著关联(G等位基因与C等位基因:OR = 1.49,95%CI = 1.08 - 2.05,异质性P < 0.01;GG与CC:OR = 2.30,95%CI = 1.05 - 5.05,异质性P < 0.01;CG与CC:OR = 1.40,95%CI = 1.03 - 1.90,异质性P < 0.01;显性模型(GG + CG与CC):OR = 1.52,95%CI = 1.06 - 2.16,异质性P < 0.01;隐性模型(GG与CG + CC):OR = 2.04,95%CI = 1.05 - 3.96,异质性P = 0.01)。按种族进行亚组荟萃分析时,排除一项不符合HWE的研究后,在白种人群中发现了显著关联(G等位基因与C等位基因:OR = 1.40,95%CI = 1.001 - 1.95,异质性P < 0.01;GG与CC:OR = 2.30,95%CI = 1.05 - 5.05,异质性P < 0.01;隐性模型(GG与CG + CC):OR = 2.04,95%CI = 1.05 - 3.96,异质性P = 0.01)。
我们的结果表明,在白种人群中,G等位基因可能与HNC风险增加相关。