Department of Urology, First Affiliated Hospital of Nanjing Medical University, Nanjing 210029, China.
Asian J Androl. 2012 Sep;14(5):726-31. doi: 10.1038/aja.2012.65. Epub 2012 Aug 20.
To determine the risk, malignant degree and clinical progression of prostate cancer (PCa) associated with mouse double-minute 2 protein (MDM2) T309G variants, a meta-analysis was performed on all eligible published studies. Odds ratios (ORs) with 95% confidence intervals (CIs) were estimated to assess these associations in seven studies that included 5151 cases and 1003 controls. In the overall analysis, the 309G allele was significantly associated with a decreased PCa risk (OR=0.85, 95% CI: 0.74-0.97); this was also the case for the homozygous comparison (OR=0.72, 95% CI: 0.55-0.95) and the dominant genetic model (OR=0.79, 95% CI: 0.65-0.96). The 309G allele was also found to be significantly associated with lower degrees of PCa malignancy (OR=0.85, 95% CI: 0.75-0.96) in the overall analysis, as well as in the heterozygous comparison (OR=0.79, 95% CI: 0.65-0.96), homozygous comparison (OR=0.76, 95% CI: 0.58-0.98) and dominant genetic model (OR=0.81, 95% CI: 0.68-0.96). Furthermore, grouping analysis showed that the 309G allele in Caucasians was significantly correlated with a decreased PCa risk (OR=0.77, 95% CI: 0.61-0.96); this was also the case in the homozygous comparison (OR=0.51, 95% CI: 0.31-0.86). The grouping analysis also showed that the 309G variant in Caucasians was significantly associated with a lower degree of PCa malignancy in all of the genetic models. In addition, we found that the 309G variant in Caucasians was significantly associated with a slower PCa clinical progression in all of the genetic models. In summary, our meta-analysis showed that the MDM2 309G variant was significantly associated with a decreased PCa risk, lower malignant degree and slower clinical progression in Caucasians, but there was no obvious association in the Asian population.
为了确定与鼠双微体 2 蛋白(MDM2)T309G 变体相关的前列腺癌(PCa)的风险、恶性程度和临床进展,对所有符合条件的已发表研究进行了荟萃分析。使用优势比(OR)和 95%置信区间(CI)来评估七个研究中的这些关联,这些研究共包括 5151 例病例和 1003 例对照。在总体分析中,309G 等位基因与 PCa 风险降低显著相关(OR=0.85,95%CI:0.74-0.97);杂合子比较(OR=0.72,95%CI:0.55-0.95)和显性遗传模型(OR=0.79,95%CI:0.65-0.96)也是如此。在总体分析中,309G 等位基因还与较低的 PCa 恶性程度显著相关(OR=0.85,95%CI:0.75-0.96),在杂合子比较(OR=0.79,95%CI:0.65-0.96)、纯合子比较(OR=0.76,95%CI:0.58-0.98)和显性遗传模型(OR=0.81,95%CI:0.68-0.96)中也是如此。此外,分组分析表明,白种人群中的 309G 等位基因与 PCa 风险降低显著相关(OR=0.77,95%CI:0.61-0.96);在纯合子比较中也是如此(OR=0.51,95%CI:0.31-0.86)。分组分析还表明,白种人群中 309G 变体与所有遗传模型中的 PCa 恶性程度较低显著相关。此外,我们发现白种人群中 309G 变体与所有遗传模型中的 PCa 临床进展速度较慢显著相关。总之,我们的荟萃分析表明,MDM2 309G 变体与白种人群中 PCa 风险降低、恶性程度降低和临床进展速度较慢显著相关,但在亚洲人群中没有明显关联。