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2
Correlations of IFN-γ genetic polymorphisms with susceptibility to breast cancer: a meta-analysis.IFN-γ基因多态性与乳腺癌易感性的相关性:一项荟萃分析。
Tumour Biol. 2014 Jul;35(7):6867-77. doi: 10.1007/s13277-014-1856-6. Epub 2014 Apr 16.
3
An association analysis of the rs1572931 polymorphism of the RAB7L1 gene in Parkinson's disease, amyotrophic lateral sclerosis and multiple system atrophy in China.中国人群中 RAB7L1 基因 rs1572931 多态性与帕金森病、肌萎缩侧索硬化症和多系统萎缩的关联分析。
Eur J Neurol. 2014 Oct;21(10):1337-43. doi: 10.1111/ene.12490. Epub 2014 Jul 12.
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ABCA transporter gene expression and poor outcome in epithelial ovarian cancer.ABCA 转运蛋白基因表达与上皮性卵巢癌不良预后的关系。
J Natl Cancer Inst. 2014 Jun 23;106(7). doi: 10.1093/jnci/dju149. Print 2014 Jul.
5
Association study between macrophage migration inhibitory factor-173 polymorphism and acute myeloid leukemia in Taiwan.台湾地区巨噬细胞移动抑制因子-173多态性与急性髓系白血病的关联性研究
Cell Biochem Biophys. 2014 Nov;70(2):1159-65. doi: 10.1007/s12013-014-0036-z.
6
Association Between Genetic Polymorphism of the MIF Gene and Colorectal Cancer in Taiwan.台湾地区MIF基因多态性与结直肠癌的关联
J Clin Lab Anal. 2015 Jul;29(4):268-74. doi: 10.1002/jcla.21763. Epub 2014 May 19.
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Macrophage migration inhibitory factor (MIF): genetic evidence for participation in early onset and early stage rheumatoid arthritis.巨噬细胞移动抑制因子(MIF):参与早发性和早期类风湿关节炎的遗传证据。
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Gastric cancer susceptibility in gastric cancer relatives: attributable risks of Macrophage migration inhibitory factor promoter polymorphism and Helicobacter pylori.胃癌亲属的胃癌易感性:巨噬细胞移动抑制因子启动子多态性和幽门螺杆菌的归因风险。
Cytokine. 2012 Nov;60(2):346-51. doi: 10.1016/j.cyto.2012.07.015. Epub 2012 Aug 11.
9
Correlation of macrophage migration inhibitory factor gene polymorphism with the risk of early-stage cervical cancer and lymphatic metastasis.巨噬细胞移动抑制因子基因多态性与早期宫颈癌及淋巴转移风险的相关性
Oncol Lett. 2011 Nov;2(6):1261-1267. doi: 10.3892/ol.2011.409. Epub 2011 Sep 2.
10
Association between macrophage migration inhibitory factor promoter region polymorphism (-173 G/C) and cancer: a meta-analysis.巨噬细胞移动抑制因子启动子区域多态性(-173 G/C)与癌症的关联:一项荟萃分析。
BMC Res Notes. 2011 Oct 11;4:395. doi: 10.1186/1756-0500-4-395.

MIF -173G/C基因多态性增加胃肠道癌和血液系统恶性肿瘤风险:一项荟萃分析和FPRP检验的证据

The MIF -173G/C gene polymorphism increase gastrointestinal cancer and hematological malignancy risk: evidence from a meta-analysis and FPRP test.

作者信息

Tong Xiang, Zheng Bing, Tong Qiaoyi, Liu Sitong, Peng Sifeng, Yang Xin, Fan Hong

机构信息

Department of Respiratory and Critical Care Medicine, West China Hospital/West China School of Medicine, Sichuan University Chengdu, Sichuan, China.

Department of Neurological Surgery, The First Affiliated Hospital of Kunming Medical University Kunming, Yunnan, China.

出版信息

Int J Clin Exp Med. 2015 Sep 15;8(9):15949-57. eCollection 2015.

PMID:26629098
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4658987/
Abstract

UNLABELLED

The macrophage migration inhibitory factor (MIF) -173G/C gene polymorphism has been implicated in the susceptibility to cancer, but the results are not conclusive. So the aim of study to investigate the association between MIF -173G/C gene polymorphism and cancer risk by a comprehensive meta-analysis. We searched the PubMed, Embase, Wanfang and China National Knowledge Internet (CNKI) databases, with the last updated search being performed on May 24, 2015. The odds ratio (OR) and 95% confidence interval (95% CI) were used to assess the association. Statistical analysis was performed by STATA 11.0 software. Finally, 7,253 participants from 15 studies were included in the meta-analysis. The results of meta-analysis indicated the significant association between MIF -173G/C gene polymorphism and cancer susceptibility, especially in Asians (C vs.

G, OR: 1.22, 95% CI=1.00-1.50). In addition, the significant relationship between MIF -173G/C gene polymorphism and gastrointestinal tumors (CC+CG vs.

GG, OR: 1.25, 95% CI=1.05-1.50), hematological malignancy (CC+CG vs.

GG, OR: 1.27, 95% CI=1.03-1.56), gynecolgical tumors (CC vs. CG+

GG, OR: 1.51, 95% CI=1.04-2.19) risk was found. However, to avoid the "false positive report", we investigated the significant associations observed in the present meta-analysis by the false positive report probabilities (FPRPs) test. Interestingly, the results of FPRP test indicated the MIF -173G/C gene polymorphism only associated with gastrointestinal cancer and hematological malignancy risk (FPRP=0.132, 0.067 respectively) at the level of a prior probability is 0.1. Therefore, the meta-analysis suggested MIF -173G/C gene polymorphism would be a risk factor for the gastrointestinal cancer and hematological malignancy.

摘要

未标注

巨噬细胞移动抑制因子(MIF)-173G/C基因多态性与癌症易感性有关,但结果尚无定论。因此,本研究旨在通过全面的荟萃分析来探究MIF -173G/C基因多态性与癌症风险之间的关联。我们检索了PubMed、Embase、万方和中国知网(CNKI)数据库,最后一次更新检索于2015年5月24日进行。采用比值比(OR)和95%置信区间(95%CI)来评估关联。使用STATA 11.0软件进行统计分析。最终,15项研究中的7253名参与者被纳入荟萃分析。荟萃分析结果表明,MIF -173G/C基因多态性与癌症易感性之间存在显著关联,尤其是在亚洲人群中(C vs. G,OR:1.22,95%CI = 1.00 - 1.50)。此外,还发现MIF -173G/C基因多态性与胃肠道肿瘤(CC + CG vs. GG,OR:1.25,95%CI = 1.05 - 1.50)、血液系统恶性肿瘤(CC + CG vs. GG,OR:1.27,95%CI = 1.03 - 1.56)、妇科肿瘤(CC vs. CG + GG,OR:1.51,95%CI = 1.04 - 2.19)风险之间存在显著关系。然而,为避免“假阳性报告”,我们通过假阳性报告概率(FPRP)检验对本荟萃分析中观察到的显著关联进行了研究。有趣的是,FPRP检验结果表明,在先验概率为0.1的水平下,MIF -173G/C基因多态性仅与胃肠道癌和血液系统恶性肿瘤风险相关(FPRP分别为0.132和0.067)。因此,荟萃分析表明MIF -173G/C基因多态性可能是胃肠道癌和血液系统恶性肿瘤的一个风险因素。