Gu Zhenwei, Wang Gang, Chen Weiguo
Department of Urology, Luzhi People's Hospital Department of Urology, Suzhou, 215127, China.
Tumour Biol. 2014 Jun;35(6):5921-30. doi: 10.1007/s13277-014-1785-4. Epub 2014 Mar 1.
Genetic and epigenetic changes in the estrogen receptor alpha (ER-α) gene, according to multiple lines of evidence, might alter its expression and its downstream signaling thereby increasing the risk of developing prostate cancer. The purpose of this meta-analysis was to determine whether polymorphisms in two intronic restriction sites in the ER-α (PvuII and XbaI) gene contribute to prostate cancer. A literature search for eligible studies published before November 5, 2013 was conducted in the PubMed, Embase, China Biology Medicine (CBM), and CNKI databases. Pooled crude odds ratios (ORs) and their corresponding 95 % confidence intervals (CIs) were calculated. Eighteen case-control and cohort studies were included in this meta-analysis with a total 4,884 prostate cancer cases and 10,134 healthy controls. Two common ER-α polymorphisms were examined: IVS1-397 C>T (a.k.a. the PvuII restriction site, rs2234693) and IVS1-351 A>G (a.k.a. the XbaI restriction site, rs9340799). Results from this meta-analysis showed that the PvuII polymorphism was not significantly associated with prostate cancer risk in any of the racial subgroups, either by allelic or genotypic frequencies. However, this meta-analysis revealed that the G allele in the XbaI polymorphism was associated with a statistically significant increase in the risk of prostate cancer. In a stratified analysis based on ethnicity, the XbaI G allele remained significantly correlated with an increased risk of prostate cancer in Africans; this correlation, however, was not found in Caucasians or Asians. In summary, a positive association correlation was observed between frequencies of the XbaI (A>G) polymorphism and prostate cancer, especially in Africans, but not such correlation was found with regard to the frequency of the PvuII (C>T) polymorphism.
根据多方面证据,雌激素受体α(ER-α)基因的遗传和表观遗传变化可能会改变其表达及其下游信号传导,从而增加患前列腺癌的风险。本荟萃分析的目的是确定ER-α基因两个内含子限制性位点(PvuII和XbaI)的多态性是否与前列腺癌有关。于2013年11月5日前发表的符合条件的研究在PubMed、Embase、中国生物医学文献数据库(CBM)和中国知网数据库中进行检索。计算合并的粗比值比(OR)及其相应的95%置信区间(CI)。本荟萃分析纳入了18项病例对照研究和队列研究,共有4884例前列腺癌病例和10134例健康对照。研究了两种常见的ER-α多态性:IVS1-397 C>T(又称PvuII限制性位点,rs2234693)和IVS1-351 A>G(又称XbaI限制性位点,rs9340799)。本荟萃分析结果显示,无论等位基因频率还是基因型频率,PvuII多态性在任何种族亚组中均与前列腺癌风险无显著相关性。然而,本荟萃分析表明,XbaI多态性中的G等位基因与前列腺癌风险的统计学显著增加相关。在基于种族的分层分析中,XbaI G等位基因与非洲人前列腺癌风险增加仍显著相关;然而,在白种人或亚洲人中未发现这种相关性。总之,观察到XbaI(A>G)多态性频率与前列腺癌之间存在正相关,尤其是在非洲人中,但未发现PvuII(C>T)多态性频率与前列腺癌存在这种相关性。