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Global MicroRNA Expression Profiling Identifies Unique MicroRNA Pattern of Radioresistant Glioblastoma Cells
J. Ondracek, P. Fadrus, J. Sana, A. Besse, T. Loja, M. Vecera, L. Radova, M. Smrcka, P. Slampa, O. Slaby,
Language English Country Greece
Document type Journal Article
Grant support
NV15-33158A
MZ0
CEP Register
NV15-34553A
MZ0
CEP Register
Digital library NLK
Full text - Article
Full text - Article
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NLK
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from 2004 to 2 years ago
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from 2004-01-01
- MeSH
- Apoptosis MeSH
- Phenotype MeSH
- Glioblastoma genetics pathology MeSH
- Humans MeSH
- MicroRNAs genetics MeSH
- Biomarkers, Tumor metabolism MeSH
- Cell Line, Tumor MeSH
- Brain Neoplasms genetics pathology MeSH
- Prognosis MeSH
- Cell Proliferation MeSH
- Gene Expression Regulation, Neoplastic * MeSH
- Oligonucleotide Array Sequence Analysis MeSH
- Gene Expression Profiling MeSH
- Radiation Tolerance genetics MeSH
- Check Tag
- Humans MeSH
- Publication type
- Journal Article MeSH
Glioblastoma multiforme (GBM) is the most aggressive intracranial tumor characterized with infaust prognosis. Despite advances in neurosurgical and radiotherapeutic techniques and chemotherapy, the median overall survival ranges between 12-15 months from diagnosis. The main cause of treatment failure is considered the presence of tumor cells resistant to conventional therapy, mainly radiotherapy. MicroRNAs (miRNAs) are small, non-coding RNAs that function as post-transcriptional regulators of gene expression and have been repeatedly proven to play important roles in pathogenesis and biological features of many cancers, including GBM and its radioresistant phenotype. In our study, we established radioresistant cells from the commonly used human GBM cell lines T98G, U87MG and U251. Consequently, we performed global miRNA expression profiling in both radioresistant and parental cell lines and identified 113 miRNAs with significantly different expression (p<0.05) between these two groups (73 miRNAs were up-regulated, 40 miRNAs were down-regulated). Some of these miRNAs have been previously described in relation to ionizing radiation, and others were herein identified for the first time. We believe that after deeper functional investigation of identified miRNAs in relation to radioresistance, these miRNAs present potential predictive biomarkers or therapeutic targets in GBM.
Central European Institute of Technology Masaryk University Brno Czech Republic
Department of Neurosurgery University Hospital Brno Masaryk University Brno Czech Republic
References provided by Crossref.org
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- $a Glioblastoma multiforme (GBM) is the most aggressive intracranial tumor characterized with infaust prognosis. Despite advances in neurosurgical and radiotherapeutic techniques and chemotherapy, the median overall survival ranges between 12-15 months from diagnosis. The main cause of treatment failure is considered the presence of tumor cells resistant to conventional therapy, mainly radiotherapy. MicroRNAs (miRNAs) are small, non-coding RNAs that function as post-transcriptional regulators of gene expression and have been repeatedly proven to play important roles in pathogenesis and biological features of many cancers, including GBM and its radioresistant phenotype. In our study, we established radioresistant cells from the commonly used human GBM cell lines T98G, U87MG and U251. Consequently, we performed global miRNA expression profiling in both radioresistant and parental cell lines and identified 113 miRNAs with significantly different expression (p<0.05) between these two groups (73 miRNAs were up-regulated, 40 miRNAs were down-regulated). Some of these miRNAs have been previously described in relation to ionizing radiation, and others were herein identified for the first time. We believe that after deeper functional investigation of identified miRNAs in relation to radioresistance, these miRNAs present potential predictive biomarkers or therapeutic targets in GBM.
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