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纤溶酶原激活物抑制剂-1启动子4G/5G多态性(rs1799768)与肿瘤易感性相关:荟萃分析证据

PAI-1 promoter 4G/5G polymorphism (rs1799768) contributes to tumor susceptibility: Evidence from meta-analysis.

作者信息

Xu Xin, Xie Yanqi, Lin Yiwei, Xu Xianglai, Zhu Yi, Mao Yeqing, Hu Zhenghui, Wu Jian, Chen Hong, Zheng Xiangyi, Qin Jie, Xie Liping

机构信息

Department of Urology, First Affiliated Hospital, School of Medicine, Zhejiang University, Hangzhou, Zhejiang 310003, P.R. China.

出版信息

Exp Ther Med. 2012 Dec;4(6):1127-1133. doi: 10.3892/etm.2012.734. Epub 2012 Oct 2.

Abstract

Plasminogen activator inhibitor-1 (PAI-1), belonging to the urokinase plasminogen activation (uPA) system, is involved in cancer development and progression. The PAI-1 promoter 4G/5G polymorphism was shown to contribute to genetic susceptibility to cancer, although the results were inconsistent. To assess this relationship more precisely, a meta-analysis was performed. The electronic databases PubMed, Scopus, Web of Science and Chinese National Knowledge Infrastructure (CNKI) were searched; data were extracted and analyzed independently by two reviewers. Ultimately, 21 eligible case-control studies with a total of 8,415 cancer cases and 9,208 controls were included. The overall odds ratio (OR) with its 95% confidence interval (CI) showed a statistically significant association between the PAI-1 promoter 4G/5G polymorphism and cancer risk (4G/4G vs. 5G/5G: OR=1.25, 95% CI=1.07-1.47, P(heterogeneity)=0.001; 4G/4G vs. 4G/5G+5G/5G: OR=1.10, 95% CI=1.03-1.17, P(heterogeneity)=0.194; 4G/4G+4G/5G vs. 5G/5G: OR=1.17, 95% CI=1.01-1.35, P(heterogeneity)=0.041). In further subgroup analyses, the increased risk of cancer was observed in a subgroup of Caucasians with regards to endometrial cancer. Our meta-analysis suggests that the PAI-1 4G/5G polymorphism most likely contributes to susceptibility to cancer, particularly in Caucasians. Furthermore, the 4G allele may be associated with an increased risk of endometrial cancer.

摘要

纤溶酶原激活物抑制剂-1(PAI-1)属于尿激酶型纤溶酶原激活系统(uPA),参与癌症的发生和发展。PAI-1启动子4G/5G多态性虽已表明与癌症遗传易感性有关,但其结果并不一致。为更精确地评估这种关系,进行了一项荟萃分析。检索了电子数据库PubMed、Scopus、Web of Science和中国知网(CNKI);由两名审阅者独立提取和分析数据。最终,纳入了21项符合条件的病例对照研究,共8415例癌症病例和9208例对照。总体比值比(OR)及其95%置信区间(CI)显示,PAI-1启动子4G/5G多态性与癌症风险之间存在统计学显著关联(4G/4G与5G/5G比较:OR = 1.25,95% CI = 1.07 - 1.47,P(异质性)= 0.001;4G/4G与4G/5G + 5G/5G比较:OR = 1.10,95% CI = 1.03 - 1.17,P(异质性)= 0.194;4G/4G + 4G/5G与5G/5G比较:OR = 1.17,95% CI = 1.01 - 1.35,P(异质性)= 0.041)。在进一步的亚组分析中,在白种人亚组中观察到子宫内膜癌的癌症风险增加。我们的荟萃分析表明,PAI-1 4G/5G多态性很可能与癌症易感性有关,尤其是在白种人中。此外,4G等位基因可能与子宫内膜癌风险增加有关。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eeed/3494103/189684a90fa6/etm-04-06-1127-g00.jpg

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