Shi Minghan, Huang Ruishan, Pei Chunying, Jia Xiuzhi, Jiang Chuanlu, Ren Huan
Department of Immunology, Harbin Medical University, Harbin 150081, P.R. China.
Oncol Lett. 2012 Mar;3(3):599-606. doi: 10.3892/ol.2011.521. Epub 2011 Dec 12.
TP53 codon 72 polymorphism has been reported to affect regulatory networks central to glioma development. Although a number of published studies noted the association between TP53 codon 72 polymorphism and glioma risk, their conclusions were inconsistent. A meta-analysis was used to assess the possible association between TP53 codon 72 polymorphism and glioma risk. The PubMed databases were searched, relevant articles were identified and data were retrieved based on the inclusion criteria. The odds ratio (OR) and 95% confidence interval (95% CI) were determined on the pooled dataset. We retrieved eight different studies including 2,260 glioma cases and 3,506 controls. However, no association was found between the TP53 codon 72 polymorphism and glioma risk regarding the comparison between glioma cases and the controls. By further stratification based on criteria such as tumor grade, and the geographical location of the patients and the relevant controls, we found a significant association in the subgroup of patients with high-grade glioma in Europeans compared to controls in two models of TP53 codon 72 polymorphism, which include the dominant model [C/C + G/C vs. G/G: OR=1.35, 95% CI (1.14, 1.59), P=0.0005, P(h)=0.13] and the additive model [C allele vs. G allele: OR=1.16, 95% CI (1.02, 1.33), P=0.03, P(h)=0.37]. Our analysis suggests that TP53 codon 72 polymorphism is associated with an increased risk of high-grade glioma development in Europeans.
据报道,TP53基因第72位密码子多态性会影响胶质瘤发生过程中的核心调控网络。尽管许多已发表的研究指出了TP53基因第72位密码子多态性与胶质瘤风险之间的关联,但其结论并不一致。本研究采用荟萃分析来评估TP53基因第72位密码子多态性与胶质瘤风险之间的可能关联。检索了PubMed数据库,根据纳入标准识别相关文章并提取数据。在汇总数据集上确定比值比(OR)和95%置信区间(95%CI)。我们检索到八项不同的研究,包括2260例胶质瘤病例和3506例对照。然而,在胶质瘤病例与对照的比较中,未发现TP53基因第72位密码子多态性与胶质瘤风险之间存在关联。通过基于肿瘤分级、患者及相关对照的地理位置等标准进行进一步分层分析,我们发现在欧洲人中,与对照相比,在TP53基因第72位密码子多态性的两种模型中,高级别胶质瘤患者亚组存在显著关联,这两种模型包括显性模型[C/C + G/C vs. G/G:OR = 1.35,95%CI(1.14,1.59),P = 0.0005,P(h)=0.13]和加性模型[C等位基因vs. G等位基因:OR = 1.16,95%CI(1.02,1.33),P = 0.03,P(h)=0.37]。我们的分析表明,TP53基因第72位密码子多态性与欧洲人高级别胶质瘤发生风险增加有关。