| Literature DB >> 32888124 |
Luiz Guilherme Darrigo Junior1, Mirella Baroni2, Régia Caroline Peixoto Lira1,3, Silvia Teixeira1, Paola Fernanda Fedatto1, Vanessa Silva Silveira2, Veridiana Kill Suazo1, Luciana Chain Veronez1, Rodrigo Alexandre Panepucci4, David Santos Marco Antônio5, José Andres Yunes6,7, Silvia Regina Brandalise6, Simone Dos Santos Aguiar7, Luciano Neder8, Ricardo Santos de Oliveira9, Hélio Rubens Machado9, Carlos Gilberto Carlotti9, Luiz Gonzaga Tone1,2, Elvis Terci Valera1, Carlos Alberto Scrideli10.
Abstract
Glioblastoma (GBM) is the most common primary malignant neoplasm of the central nervous system and, despite the standard therapy; the patients' prognoses remain dismal. The miRNA expression profiles have been associated with patient prognosis, suggesting that they may be helpful for tumor diagnosis and classification as well as predictive of tumor response to treatment. We described the microRNA expression profile of 29 primary GBM samples (9 pediatric GBMs) and 11 non-neoplastic white matter samples as controls (WM) by microarray analysis and we performed functional in vitro assays on these 2 most differentially expressed miRNAs. Hierarchical clustering analysis showed 3 distinct miRNA profiles, two of them in the GBM samples and a group consisting only of cerebral white matter. When adult and pediatric GBMs were compared to WM, 37 human miRNAs were found to be differentially expressed, with miR-10b-5p being the most overexpressed and miR-630 the most underexpressed. The overexpression of miR-630 was associated with reduced cell proliferation and invasion in the U87 GBM cell line, whereas the inhibition of miR-10b-5p reduced cell proliferation and colony formation in the U251 GBM cell line, suggesting that these miRNAs may act as tumor-suppressive and oncogenic miRNAs, respectively. The present study highlights the distinct epigenetic profiling of adult and pediatric GBMs and underscores the biological importance of mir-10b-5p and miR-630 for the pathobiology of these lethal tumors.Entities:
Keywords: Glioblastoma; miR-10b; miR-630; miRNA
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Year: 2020 PMID: 32888124 DOI: 10.1007/s11033-020-05754-3
Source DB: PubMed Journal: Mol Biol Rep ISSN: 0301-4851 Impact factor: 2.316