Zhou Tian-Biao, Yin Sheng-Sheng, Huang Jian-Jian, Ou Chao
Department of Experimental Pathology, The Affiliated Tumor Hospital of Guangxi Medical University, Nanning, China.
Asian Pac J Cancer Prev. 2012;13(7):3319-23. doi: 10.7314/apjcp.2012.13.7.3319.
The results from the published studies on the association between prohibitin 3' untranslated region C > T gene polymorphism and cancer risk are conflicting. This meta-analysis was performed to evaluate the relationship with cancer susceptibility overall, and to explore whether the T allele or TT genotype could become a predictive marker for cancer risk.
Association studies were identified from the databases of PubMed, Embase, and Cochrane Library as of March 1, 2012, and eligible investigations were synthesized using the meta-analysis method. Results were expressed with odds ratios (OR) for dichotomous data, and 95% confidence intervals (CI) were also calculated.
Six investigations were identified for the analysis of association between the prohibitin 3' untranslated region C > T gene polymorphism and cancer risk, covering of 1,461 patients with cancer and 1,197 controls. There was a positive association between the T allele and cancer susceptibility (OR=1.20, 95% CI: 1.03-1.39, P=0.02), and CC homozygous might play a protective role (OR=0.80, 95% CI: 0.68-6.11, P=0.95). In the sub-group analysis, prohibitin 3' untranslated region C > T gene polymorphism and cancer risk appeared associated with the risk of breast cancer, but not ovarian cancer.
Our results indicate that T allele is a significant genetic molecular marker to predict cancer susceptibility and CC genotype is protective, especially for breast cancer. However, more investigations are required to further clarify the association of the prohibitin 3' untranslated region C > T gene polymorphism with cancer susceptibility.
已发表的关于抑制素3'非翻译区C>T基因多态性与癌症风险之间关联的研究结果相互矛盾。本荟萃分析旨在评估其与总体癌症易感性的关系,并探讨T等位基因或TT基因型是否可成为癌症风险的预测标志物。
检索截至2012年3月1日的PubMed、Embase和Cochrane图书馆数据库中的关联研究,并使用荟萃分析方法综合符合条件的研究。二分类数据的结果以比值比(OR)表示,并计算95%置信区间(CI)。
确定了6项关于抑制素3'非翻译区C>T基因多态性与癌症风险关联分析的研究,涵盖1461例癌症患者和1197例对照。T等位基因与癌症易感性呈正相关(OR=1.20,95%CI:1.03-1.39,P=0.02),CC纯合子可能起保护作用(OR=0.80,95%CI:0.68-6.11,P=0.95)。在亚组分析中,抑制素3'非翻译区C>T基因多态性与癌症风险似乎与乳腺癌风险相关,但与卵巢癌无关。
我们的结果表明,T等位基因是预测癌症易感性的重要遗传分子标志物,CC基因型具有保护作用,尤其是对乳腺癌。然而,需要更多的研究来进一步阐明抑制素3'非翻译区C>T基因多态性与癌症易感性的关联。