Pan Feng, Tian Jing, Ji Chu-Shu, He Yi-Fu, Han Xing-Hua, Wang Yong, Du Jian-Ping, Jiang Feng-Shou, Zhang Ying, Pan Yue-Yin, Hu Bing
Department of Oncology, Anhui Provincial Hospital affiliated to Anhui Medical University, Hefei, China.
Asian Pac J Cancer Prev. 2012;13(11):5777-83. doi: 10.7314/apjcp.2012.13.11.5777.
Published data on the associations between tumor necrosis factor-alpha (TNF-α) promoter -308G>A and -238G>A polymorphisms and cervical cancer risk are inconclusive. To derive a more precise estimation of the relationship, a meta-analysis was performed. Data were collected from MEDLINE and PubMed databases. Crude odds ratios (ORs) with 95% confidence intervals (CIs) were calculated in a fixed/random effect model. 13 separate studies including 3294 cases and 3468 controls were involved in the meta-analysis. We found no association between TNF-α-308G>A polymorphism and cervical cancer in overall population. In subgroup analysis, significantly elevated risks were found in Caucasian population (A vs. G: OR=1.43, 95% CI=1.00- 2.03; AA vs. GG: OR=2.09, 95% CI=1.34-3.25; Recessive model: OR=2.09, 95% CI=1.35-3.25) and African population (GA vs. GG: OR=1.53, 95% CI=1.02-2.30). An association of TNF-α-238G>A polymorphism with cervical cancer was found (A vs. G: OR=0.61, 95% CI=0.47-0.78; GA vs. GG: OR=0.59, 95% CI=0.45-0.77; Dominant model: OR=0.59, 95% CI=0.46-0.77). When stratified by ethnicity, similar association was observed in Caucasian population (A vs. G: OR=0.62, 95% CI=0.46-0.84; GA vs. GG: OR=0.59, 95% CI=0.43-0.82; Dominant model: OR=0.60, 95% CI=0.44-0.83). In summary, this meta-analysis suggests that TNF-α-238A allele significantly decreased the cervical cancer risk, and the TNF-α-308G>A polymorphism is associated with the susceptibility to cervical cancer in Caucasian and African population.
已发表的关于肿瘤坏死因子-α(TNF-α)启动子-308G>A和-238G>A多态性与宫颈癌风险之间关联的数据尚无定论。为了更精确地估计两者之间的关系,我们进行了一项荟萃分析。数据收集自MEDLINE和PubMed数据库。采用固定/随机效应模型计算粗比值比(OR)及95%置信区间(CI)。该荟萃分析纳入了13项独立研究,包括3294例病例和3468例对照。我们发现,在总体人群中,TNF-α -308G>A多态性与宫颈癌之间无关联。亚组分析显示,在白种人群(A vs. G:OR=1.43,95%CI=1.00 - 2.03;AA vs. GG:OR=2.09,95%CI=1.34 - 3.25;隐性模型:OR=2.09,95%CI=1.35 - 3.25)和非洲人群(GA vs. GG:OR=1.53,95%CI=1.02 - 2.30)中,风险显著升高。我们发现TNF-α -238G>A多态性与宫颈癌存在关联(A vs. G:OR=0.61,95%CI=0.47 - 0.78;GA vs. GG:OR=0.59,95%CI=0.45 - 0.77;显性模型:OR=0.59,95%CI=0.46 - 0.77)。按种族分层时,在白种人群中观察到类似的关联(A vs. G:OR=0.62,95%CI=0.46 - 0.84;GA vs. GG:OR=0.59,95%CI=0.43 - 0.82;显性模型:OR=0.60,95%CI=0.44 - 0.83)。总之,该荟萃分析表明,TNF-α -238A等位基因可显著降低宫颈癌风险,而TNF-α -308G>A多态性与白种人和非洲人群患宫颈癌的易感性相关。