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循环miR-21的诊断价值:多种癌症的最新荟萃分析及子宫内膜癌中的验证

Diagnostic value of circulating miR-21: An update meta-analysis in various cancers and validation in endometrial cancer.

作者信息

Gao Yun, Dai Meiyu, Liu Haihua, He Wangjiao, Lin Shengzhang, Yuan Tianzhu, Chen Hong, Dai Shengming

机构信息

Medical Science Laboratory, the Fourth Affiliated Hospital of Guangxi Medical University, Liuzhou, Guangxi 545005, China.

Department of Thoracic Surgery, the Fourth Affiliated Hospital of Guangxi Medical University, Liuzhou, Guangxi 545005, China.

出版信息

Oncotarget. 2016 Oct 18;7(42):68894-68908. doi: 10.18632/oncotarget.12028.

DOI:10.18632/oncotarget.12028
PMID:27655698
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5356598/
Abstract

MiR-21 has been identified as one of the most common proto-oncogenes. It is hypothesized that up-regulated miR-21 could be served as a potential biomarker for human cancer diagnosis. However, inconsistencies or discrepancies about diagnostic accuracy of circulating miR-21 still remain. In this sense, miR-21's diagnostic value needs to be fully validated. In this study, we performed an update meta-analysis to estimate the diagnostic value of circulating miR-21 in various human cancers. Additionally, we conducted a validation test on 50 endometrial cancer patients, 50 benign lesion patients and 50 healthy controls. A systematical literature search for relevant articles was performed in Pubmed, Embase and Cochrane Library. A total of 48 studies from 39 articles, involving 3,568 cancer patients and 2,248 controls, were included in this meta-analysis. The overall sensitivity, specificity, positive likelihood ratio (PLR), negative likelihood ratio (NLR), diagnostic odds ratio (DOR) and area under the curve (AUC) were 0.76 (0.71-0.80), 0.82 (0.79-0.85), 4.3 (3.6-5.1), 0.29 (0.24-0.35), 15 (11-20) and 0.86 (0.83-0.89), respectively. In the validation test, the expression levels of serum miR-21 were significantly higher in benign lesion patients (p = 0.003) and endometrial cancer patients (p = 0.000) compared with that of healthy controls. Endometrial cancer patients showed higher miR-21 expression levels (p = 0.000) compared with benign lesion patients. In conclusion, the meta-analysis shows that circulating miR-21 has excellent performance on the diagnosis for various cancers and the validation test demonstrates that serum miR-21 could be served as a novel biomarker for endometrial carcinoma.

摘要

MiR-21已被确定为最常见的原癌基因之一。据推测,上调的MiR-21可能作为人类癌症诊断的潜在生物标志物。然而,关于循环MiR-21诊断准确性的不一致或差异仍然存在。从这个意义上说,MiR-21的诊断价值需要得到充分验证。在本研究中,我们进行了一项更新的荟萃分析,以评估循环MiR-21在各种人类癌症中的诊断价值。此外,我们对50例子宫内膜癌患者、50例良性病变患者和50例健康对照进行了验证试验。在Pubmed、Embase和Cochrane图书馆中对相关文章进行了系统的文献检索。本荟萃分析共纳入了39篇文章中的48项研究,涉及3568例癌症患者和2248例对照。总体敏感性、特异性、阳性似然比(PLR)、阴性似然比(NLR)、诊断比值比(DOR)和曲线下面积(AUC)分别为0.76(0.71-0.80)、0.82(0.79-0.85)、4.3(3.6-5.1)、0.29(0.24-0.35)、15(11-20)和0.86(0.83-0.89)。在验证试验中,与健康对照相比,良性病变患者(p = 0.003)和子宫内膜癌患者(p = 0.000)血清MiR-21的表达水平显著更高。与良性病变患者相比,子宫内膜癌患者的MiR-21表达水平更高(p = 0.000)。总之,荟萃分析表明循环MiR-21在各种癌症诊断中具有优异的性能,验证试验表明血清MiR-21可作为子宫内膜癌的一种新型生物标志物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0f35/5356598/8d5653856b1f/oncotarget-07-68894-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0f35/5356598/750e8a3dd50c/oncotarget-07-68894-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0f35/5356598/ed72deaa57ce/oncotarget-07-68894-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0f35/5356598/d202277bcb72/oncotarget-07-68894-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0f35/5356598/8dd4ae7b335a/oncotarget-07-68894-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0f35/5356598/bd63f6cb67eb/oncotarget-07-68894-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0f35/5356598/8d5653856b1f/oncotarget-07-68894-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0f35/5356598/750e8a3dd50c/oncotarget-07-68894-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0f35/5356598/ed72deaa57ce/oncotarget-07-68894-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0f35/5356598/d202277bcb72/oncotarget-07-68894-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0f35/5356598/8dd4ae7b335a/oncotarget-07-68894-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0f35/5356598/bd63f6cb67eb/oncotarget-07-68894-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0f35/5356598/8d5653856b1f/oncotarget-07-68894-g006.jpg

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