Laboratory of Medical Genetics, Harbin Medical University, Baojian Road 157, Nangang District, Harbin 150081, China.
Breast Cancer Res Treat. 2011 Apr;126(3):763-70. doi: 10.1007/s10549-010-1184-5. Epub 2010 Sep 30.
We conducted a meta-analysis to assess the association between tumor necrosis factor-alpha (TNF-alpha) gene TNFA -308 (G>A), TNFA -238 (G>A), TNFA -857 (C>T), TNFA -863 (C>A), TNFA -1031 (T>C), TNFA -1210 (A>T) polymorphisms and breast cancer(BC) susceptibility. We also performed subgroup analyses based on ethnicity (Caucasian, Asian, and African). An extensive search was performed to identify all case-control studies investigating such association. Thirteen eligible studies, including 10,236 BC patients and 13,143 controls, were identified. No significant association was observed in all genotypes in worldwide populations, but stratification by ethnicity indicated that the TNFA -308 A allele was associated with a decreased risk of BC compared with the G allele in Caucasian individuals (OR = 0.927, 95%CI = 0.879-0.978). Similar results were obtained when the A/A +A/G genotype was compared with the G/G genotype. In addition, meta-analysis results indicated that the A/A genotype of TNFA -308 was a risk factor for BC in African (A/A vs. G/G OR = 4.085 95%CI = 1.460-11.425; A/A vs. G/A OR = 4.861 95%CI = 1.746-13.527; A/A vs. G/A + G/G OR = 4.246 95%CI = 1.551-11.625), but not in Caucasian or Asian individuals. In conclusion, the results of this meta-analysis indicate that the TNFA -308 A allele may be an important protective factor for BC in European individuals, but it is not likely to confer susceptibility to BC in worldwide populations. In addition, the AA genotype of TNFA -308 may be a risk factor for BC in African individuals. Besides, other polymorphisms were not associated with BC susceptibility.
我们进行了一项荟萃分析,以评估肿瘤坏死因子-α(TNF-α)基因 TNFA-308(G>A)、TNFA-238(G>A)、TNFA-857(C>T)、TNFA-863(C>A)、TNFA-1031(T>C)、TNFA-1210(A>T)多态性与乳腺癌(BC)易感性之间的关联。我们还根据种族(白种人、亚洲人和非洲人)进行了亚组分析。进行了广泛的搜索,以确定所有研究这种关联的病例对照研究。确定了 13 项符合条件的研究,包括 10236 名 BC 患者和 13143 名对照者。在全球人群的所有基因型中均未观察到显著关联,但按种族分层表明,与白种人相比,TNFA-308 的 A 等位基因与 BC 的风险降低相关(OR=0.927,95%CI=0.879-0.978)。当比较 A/A+A/G 基因型与 G/G 基因型时,也得到了类似的结果。此外,荟萃分析结果表明,TNFA-308 的 A/A 基因型是非洲人 BC 的危险因素(A/A 与 G/G 的 OR=4.085,95%CI=1.460-11.425;A/A 与 A/A+G/G 的 OR=4.861,95%CI=1.746-13.527;A/A 与 A/A+G/G 的 OR=4.246,95%CI=1.551-11.625),但在白种人和亚洲人中并非如此。总之,这项荟萃分析的结果表明,TNFA-308 的 A 等位基因可能是欧洲人 BC 的一个重要保护因素,但不太可能使全球人群易患 BC。此外,TNFA-308 的 AA 基因型可能是非洲人 BC 的危险因素。此外,其他多态性与 BC 易感性无关。