Gao Jie, Yang Peng-Tao, Diao Yan, Kang Hua-Feng, Zhao Yang, Lin Shuai, Wang Zi-Ming, Wang Meng, Wang Xi-Jing, Dai Zhi-Jun
Department of Oncology, The Second Affiliated Hospital of Xi'an Jiaotong University Xi'an 710004, China ; Department of Nephrology, The Second Affiliated Hospital of Xi'an Jiaotong University Xi'an 710004, China.
Department of Oncology, The Second Affiliated Hospital of Xi'an Jiaotong University Xi'an 710004, China.
Int J Clin Exp Med. 2015 Feb 15;8(2):2156-64. eCollection 2015.
Previous studies have investigated the associations between the two polymorphisms (prostate stem cell antigen (PSCA) rs2294008 C/T and c-MYC rs9642880 G/T) and bladder cancer (BC) risk. However, the results are inconsistent. We therefore carried out a meta-analysis to estimate the relationship between PSCA/c-MYC polymorphisms and BC risk. We searched PubMed up to November 2014 to identify potentially eligible literatures. Odds ratios (ORs) and 95% confidence intervals (CIs) were used to estimate the strength of the associations, the data were further stratified by ethnicity. Heterogeneity was evaluated by Q test and I(2) statistics. Begg's funnel plot and Egger's test were used to assess the publication bias. 11 studies from 9 articles were identified, including a total of 16,814 cancer cases and 52,868 case-free controls. We found a significant association between PSCA rs2294008 polymorphism and BC risk (the allele contrast model: OR = 1.14, 95% CI = 1.11-1.18; homozygote comparison: OR = 1.28, 95% CI = 1.20-1.37; heterozygote comparison: OR = 1.23, 95% CI = 1.17-1.30; dominant model: OR = 1.25, 95% CI = 1.19-1.31 and recessive model: OR = 1.13, 95% CI = 1.07-1.20). Moreover, a significant increased risk of BC was confirmed both in Caucasian and in Asians. For c-MYC rs9642880 polymorphism, significant increased BC risk was detected under the following genetic models (the allele contrast model: OR = 1.20, 95% CI = 1.13-1.27; homozygote comparison: OR = 1.37, 95% CI = 1.21-1.55; heterozygote comparison: OR = 1.20, 95% CI = 1.09-1.32; dominant model: OR = 1.25, 95% CI = 1.14-1.37 and recessive model: OR = 1.26, 95% CI = 1.13-1.40). Further stratified analysis by ethnicity also observed the same results. This meta-analysis suggested that PSCA rs2294008 and c-MYC rs9642880 polymorphisms may increase the BC risk. Further studies are needed to clarify the effects.
以往研究调查了两种多态性(前列腺干细胞抗原(PSCA)rs2294008 C/T和c-MYC rs9642880 G/T)与膀胱癌(BC)风险之间的关联。然而,结果并不一致。因此,我们进行了一项荟萃分析,以评估PSCA/c-MYC多态性与BC风险之间的关系。我们检索了截至2014年11月的PubMed,以确定潜在符合条件的文献。采用优势比(OR)和95%置信区间(CI)来估计关联强度,数据进一步按种族分层。通过Q检验和I²统计量评估异质性。使用Begg漏斗图和Egger检验评估发表偏倚。从9篇文章中鉴定出11项研究,共包括16,814例癌症病例和52,868例无癌对照。我们发现PSCA rs2294008多态性与BC风险之间存在显著关联(等位基因对比模型:OR = 1.14,95% CI = 1.11 - 1.18;纯合子比较:OR = 1.28,95% CI = 1.20 - 1.37;杂合子比较:OR = 1.23,95% CI = 1.17 - 1.30;显性模型:OR = 1.25,95% CI = 1.19 - 1.31;隐性模型:OR = 1.13,95% CI = 1.07 - 1.20)。此外,在白种人和亚洲人中均证实BC风险显著增加。对于c-MYC rs9642880多态性,在以下遗传模型下检测到BC风险显著增加(等位基因对比模型:OR = 1.20,95% CI = 1.13 - 1.27;纯合子比较:OR = 1.37,95% CI = 1.21 - 1.55;杂合子比较:OR = 1.20,95% CI = (1.09 - 1.32);显性模型:OR = 1.25,95% CI = 1.14 - 1.37;隐性模型:OR = 1.26,95% CI = 1.13 - 1.40)。按种族进行的进一步分层分析也观察到相同结果。这项荟萃分析表明,PSCA rs2294008和c-MYC rs9642880多态性可能会增加BC风险。需要进一步研究来阐明其影响。 (注:原文中“杂合子比较:OR = 1.20,95% CI = (1.09 - 1.32)”括号为译者添加,原文此处括号使用不规范,推测是遗漏括号,补充后使格式完整。)