Identification of Deregulated miRNAs and mRNAs Involved in Tumorigenesis and Detection of Glioblastoma Patients Applying Next-Generation RNA Sequencing

被引:0
作者
Geczi, Dora [1 ]
Klekner, Almos [2 ]
Balogh, Istvan [1 ,3 ]
Penyige, Andras [1 ]
Szilagyi, Melinda [1 ]
Virga, Jozsef [4 ]
Bako, Andrea [4 ]
Nagy, Balint [1 ]
Torner, Bernadett [1 ]
Birko, Zsuzsanna [1 ]
机构
[1] Univ Debrecen, Fac Med, Dept Human Genet, H-4032 Debrecen, Hungary
[2] Univ Debrecen, Fac Med, Dept Neurosurg, H-4032 Debrecen, Hungary
[3] Univ Debrecen, Fac Med, Dept Lab Med, Div Clin Genet, H-4032 Debrecen, Hungary
[4] Univ Debrecen, Fac Med, Dept Oncol, H-4032 Debrecen, Hungary
关键词
glioblastoma; miRNAs; brain tissue; next-generation sequencing; biomarker; TUMOR-SUPPRESSOR; GLIOMA-CELLS; EXPRESSION; INHIBITION; MICRORNAS; GROWTH; GENES; PROLIFERATION; MULTIFORME; APOPTOSIS;
D O I
10.3390/ph18030431
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
(1) Background: Glioblastoma (GBM) is one of the most aggressive brain tumors with a poor prognosis. Therefore, new insights into GBM diagnosis and treatment are required. In addition to differentially expressed mRNAs, miRNAs may have the potential to be applied as diagnostic biomarkers. (2) Methods: In this study, profiling of human miRNAs in combination with mRNAs was performed on total RNA isolated from tissue samples of five control and five GBM patients, using a high-throughput RNA sequencing (RNA-Seq) approach. (3) Results: A total of 35 miRNAs and 365 mRNAs were upregulated, while 82 miRNAs and 1225 mRNAs showed significant downregulation between tissue samples of GBM patients compared to the control samples using the iDEP tool to analyze RNA-Seq data. To validate our results, the expression of five miRNAs (hsa-miR-196a-5p, hsa-miR-21-3p, hsa-miR-10b-3p, hsa-miR-383-5p, and hsa-miR-490-3p) and fourteen mRNAs (E2F2, HOXD13, VEGFA, CDC45, AURKB, HOXC10, MYBL2, FABP6, PRLHR, NEUROD6, CBLN1, HRH3, HCN1, and RELN) was determined by RT-qPCR assay. The miRNet tool was used to build miRNA-target interaction. Furthermore, a protein-protein interaction (PPI) network was created from the miRNA targets by applying the NetworkAnalyst 3.0 tool. Based on the PPI network, a functional enrichment analysis of the target proteins was also carried out. (4) Conclusions: We identified an miRNA panel and several deregulated mRNAs that could play an important role in tumor development and distinguish GBM patients from healthy controls with high sensitivity and specificity using total RNA isolated from tissue samples.
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页数:29
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