Yang Xi, Zhao Fen, Li Yue-Hua, Huang Min, Huang Ying, Yi Cheng
Department of Abdominal Cancer, Cancer Center, West China Hospital, Sichuan University, Chengdu, Sichuan Province, China E-mail :
Asian Pac J Cancer Prev. 2014;15(22):9693-8. doi: 10.7314/apjcp.2014.15.22.9693.
Associations between the 8473T>C polymorphism (rs5275) in the cyclooxygenase-2 (COX-2) gene and breast cancer (BC) risk are still inconclusive and ambiguous. The aim of this meta-analysis was to comprehensively estimate the genetic risk of 8473T>C polymorphism in the COX-2 gene for BC.
We searched PubMed, Web of Science, Medline, Chinese biomedical (CBM), Weipu, China national knowledge infrastructure (CNKI), and Wanfang databases, covering all publications (last search was updated on Aug 17, 2014). Statistical analyses were performed using Revman 5.3 and STATA 10.0 software.
A total of 6,720 cases and 9,794 controls in 12 studies were included in this study. The results indicated no significant associations between the 8473T>C polymorphism of the COX-2 gene and BC risk for the CC+TC vs TT model (pooled odds ratio (OR)=0.97, 95% confidence interval (CI)=0.90-1.03, and p=0.29). On subgroup analysis, we also found that subdivision on ethnicity among Caucasians, Asians and others also revealed no relationship with BC susceptibility. With the study design (CC+TC vs TT), no significant associations were found in either population-based case-control studies (PCC), or hospital-based case-control studies (HCC).
This present meta-analysis suggests that the 8473T>C polymorphism in the COX-2 gene is not a conspicuous low- penetrant risk factor for developing BC.
环氧化酶-2(COX-2)基因8473T>C多态性(rs5275)与乳腺癌(BC)风险之间的关联仍不明确且存在争议。本荟萃分析的目的是全面评估COX-2基因8473T>C多态性对BC的遗传风险。
我们检索了PubMed、Web of Science、Medline、中国生物医学文献数据库(CBM)、维普、中国知网(CNKI)和万方数据库,涵盖所有出版物(最后一次检索更新于2014年8月17日)。使用Revman 5.3和STATA 10.0软件进行统计分析。
本研究纳入了12项研究中的6720例病例和9794例对照。结果表明,在CC+TC与TT模型中,COX-2基因的8473T>C多态性与BC风险之间无显著关联(合并比值比(OR)=0.97,95%置信区间(CI)=0.90-1.03,p=0.29)。亚组分析中,我们还发现按白种人、亚洲人和其他种族进行细分,也未发现与BC易感性有关。采用该研究设计(CC+TC与TT),在基于人群的病例对照研究(PCC)或基于医院的病例对照研究(HCC)中均未发现显著关联。
本荟萃分析表明,COX-2基因的8473T>C多态性不是BC发生的显著低 penetrant风险因素。 (注:原文中“low- penetrant”可能有误,推测可能是“low-penetrance”,低外显率 ,这里按原文翻译)