miRNA microarray reveals specific expression in the peripheral blood of glioblastoma patients

被引:96
作者
Dong, Lun [1 ]
Li, Yuping [1 ]
Han, Chongxu [2 ]
Wang, Xiaodong [1 ]
She, Lei [1 ]
Zhang, Hengzhu [1 ]
机构
[1] Yangzhou Univ, Clin Med Coll, Dept Neurosurg, Yangzhou 225001, Jiangsu, Peoples R China
[2] Yangzhou Univ, Clin Med Coll, Dept Cent Lab, Yangzhou 225001, Jiangsu, Peoples R China
关键词
glioma; microRNA; microarray; pathway; blood; CIRCULATING MICRORNA; CANCER; PROFILES; BIOGENESIS; BIOMARKERS; DIAGNOSIS; SERUM;
D O I
10.3892/ijo.2014.2459
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
MicroRNAs (miRNAs) are frequently dysregulated in glioblastoma (GBM) patients. It has been discovered that highly stable extracellular miRNAs circulate in the blood of both healthy individuals and patients. miRNAs in serum of patients with GBM and normal controls were analyzed by microarray analysis. The relevant bioinformatic analysis of the predicted target genes (gene ontology, pathway, gene network analysis) were performed. The miRNA microarray reveals differentially expressed miRNAs in serum between the GBM and normal controls. Of the 752 miRNAs, 115 miRNAs were upregulated in the GBM group, and 24 miRNAs were down-regulated (fold change >= 2.0 P<0.01). By further analysis, we found that miR-576-5p, miR-340 and miR-626 were significantly overexpressed, but miR-320, let-7g-5p and miR-7-5P showed significantly low expression in GBM patients. By further bioinformatic analysis, we found that they possibly play important roles in the regulation of glioma signaling pathways. In summary, the six miRNAs are significant distinct in the peripheral blood of patients with GBM pathologies. These data suggest that the miRNA profile of the peripheral blood may serve as a new biomarker for glioma diagnosis with high specificity and sensitivity.
引用
收藏
页码:746 / 756
页数:11
相关论文
共 37 条
[1]   Investigation of miR-21, miR-141, and miR-221 in blood circulation of patients with prostate cancer [J].
Agaoglu, Fulya Yaman ;
Kovancilar, Muge ;
Dizdar, Yavuz ;
Darendeliler, Emin ;
Holdenrieder, Stefan ;
Dalay, Nejat ;
Gezer, Ugur .
TUMOR BIOLOGY, 2011, 32 (03) :583-588
[2]   The functions of animal microRNAs [J].
Ambros, V .
NATURE, 2004, 431 (7006) :350-355
[3]   The Promise of MicroRNA Replacement Therapy [J].
Bader, Andreas G. ;
Brown, David ;
Winkler, Matthew .
CANCER RESEARCH, 2010, 70 (18) :7027-7030
[4]   MicroRNAs: Genomics, biogenesis, mechanism, and function (Reprinted from Cell, vol 116, pg 281-297, 2004) [J].
Bartel, David P. .
CELL, 2007, 131 (04) :11-29
[5]   bantam encodes a developmentally regulated microRNA that controls cell proliferation and regulates the proapoptotic gene hid in Drosophila [J].
Brennecke, J ;
Hipfner, DR ;
Stark, A ;
Russell, RB ;
Cohen, SM .
CELL, 2003, 113 (01) :25-36
[6]   Characterization of microRNAs in serum: a novel class of biomarkers for diagnosis of cancer and other diseases [J].
Chen, Xi ;
Ba, Yi ;
Ma, Lijia ;
Cai, Xing ;
Yin, Yuan ;
Wang, Kehui ;
Guo, Jigang ;
Zhang, Yujing ;
Chen, Jiangning ;
Guo, Xing ;
Li, Qibin ;
Li, Xiaoying ;
Wang, Wenjing ;
Zhang, Yan ;
Wang, Jin ;
Jiang, Xueyuan ;
Xiang, Yang ;
Xu, Chen ;
Zheng, Pingping ;
Zhang, Juanbin ;
Li, Ruiqiang ;
Zhang, Hongjie ;
Shang, Xiaobin ;
Gong, Ting ;
Ning, Guang ;
Wang, Jun ;
Zen, Ke ;
Zhang, Junfeng ;
Zhang, Chen-Yu .
CELL RESEARCH, 2008, 18 (10) :997-1006
[7]   Reproducibility of quantitative RT-PCR array in miRNA expression profiling and comparison with microarray analysis [J].
Chen, Yongxin ;
Gelfond, Jonathan A. L. ;
McManus, Linda M. ;
Shireman, Paula K. .
BMC GENOMICS, 2009, 10 :407
[8]   Circulating Plasma MiR-141 Is a Novel Biomarker for Metastatic Colon Cancer and Predicts Poor Prognosis [J].
Cheng, Hanyin ;
Zhang, Lina ;
Cogdell, David E. ;
Zheng, Hong ;
Schetter, Aaron J. ;
Nykter, Matti ;
Harris, Curtis C. ;
Chen, Kexin ;
Hamilton, Stanley R. ;
Zhang, Wei .
PLOS ONE, 2011, 6 (03)
[9]   MicroRNAs and endocrine biology [J].
Cuellar, TL ;
McManus, MT .
JOURNAL OF ENDOCRINOLOGY, 2005, 187 (03) :327-332
[10]   Characterization of microRNA expression profiles in normal and osteoarthritic human chondrocytes [J].
Diaz-Prado, Silvia ;
Cicione, Claudia ;
Muinos-Lopez, Emma ;
Hermida-Gomez, Tamara ;
Oreiro, Natividad ;
Fernandez-Lopez, Carlos ;
Blanco, Francisco J. .
BMC MUSCULOSKELETAL DISORDERS, 2012, 13