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Prognostic role of microRNA-31 in various cancers: a meta-analysis.

作者信息

Wang Shuwei, Hu Jun, Zhang Dongsheng, Li Juan, Fei Qiang, Sun Yueming

机构信息

Department of Colorectal Surgery, The First Affiliated Hospital of Nanjing Medical University, 300 Guangzhou Road, Nanjing, 210029, People's Republic of China.

出版信息

Tumour Biol. 2014 Nov;35(11):11639-45. doi: 10.1007/s13277-014-2492-x. Epub 2014 Aug 20.


DOI:10.1007/s13277-014-2492-x
PMID:25139099
Abstract

To date, many studies have shown that microRNAs (miRNA) exhibit altered expression levels in various cancers and may play a potential role as diagnostic and prognostic biomarkers of cancers. This meta-analysis was designed to evaluate the exact role of microRNA-31 (miR-31) for survival and discuss the possibility of utilizing miR-31 to predict the prognosis of patients with various human cancers. Electronic literature databases including PubMed, Web of Science, and Embase were searched for articles published until May 2014. The articles only written in English were considered. Data were extracted from studies comparing overall survival (OS), cancer-specific survival (CSS), or postoperative survival (PS) in patients with multiple cancers, which showed higher miR-31 expression than with similar patients. Pooled hazard ratios (HRs) of miR-31 for survival and 95 % confidence intervals (CI) were calculated. Ten studies with a total of 1,648 participants were included for the meta-analysis. For OS, the pooled HRs of higher miR-31 expression in cancers indicated significant predictor poorer survival in general cancers in either univariate analysis (HR=2.34, 95 % CI=1.15-3.52, P<0.05) or multivariate analysis (HR=1.15, 95 % CI=1.04-1.26, P<0.05). For CSS, elevated miR-31 was also a significant predictor to general cancers in multivariate analysis (HR=1.77, 95 % CI=1.06-2.47, P<0.05). And, no association was found between miR-31 expression and PS. In conclusion, the present findings indicate that high miR-31 expression is associated with poor OS and CSS in patients with general cancers and miR-31 may be a useful clinical prognostic biomarker.

摘要

相似文献

[1]
Prognostic role of microRNA-31 in various cancers: a meta-analysis.

Tumour Biol. 2014-11

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[6]
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[7]
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[8]
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[9]
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[5]
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[6]
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[7]
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[8]
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[9]
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[10]
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本文引用的文献

[1]
MicroRNA-141 promotes the proliferation of non-small cell lung cancer cells by regulating expression of PHLPP1 and PHLPP2.

FEBS Lett. 2014-8-25

[2]
Role of microRNAs in gastric cancer.

World J Gastroenterol. 2014-5-21

[3]
MiR-31 is an independent prognostic factor and functions as an oncomir in cervical cancer via targeting ARID1A.

Gynecol Oncol. 2014-4-30

[4]
microRNA 31 functions as an endometrial cancer oncogene by suppressing Hippo tumor suppressor pathway.

Mol Cancer. 2014-4-29

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MicroRNA-203 inhibits the progression of esophageal squamous cell carcinoma with restored epithelial tissue architecture in vivo.

Int J Oncol. 2014-6

[6]
Differentially expressed miRNAs in Ewing sarcoma compared to mesenchymal stem cells: low miR-31 expression with effects on proliferation and invasion.

PLoS One. 2014-3-25

[7]
The breast cancer oncogene EMSY represses transcription of antimetastatic microRNA miR-31.

Mol Cell. 2014-2-27

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Decreased circulating miR-375: a potential biomarker for patients with non-small-cell lung cancer.

Gene. 2014-1-15

[9]
Elevated microRNA-31 expression regulates colorectal cancer progression by repressing its target gene SATB2.

PLoS One. 2013-12-30

[10]
Concomitant microRNA-31 downregulation and radixin upregulation predicts advanced tumor progression and unfavorable prognosis in patients with gliomas.

J Neurol Sci. 2014-3-15

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