| Literature DB >> 25322872 |
Jiri Sana1, Lenka Radova2, Radek Lakomy3, Leos Kren4, Pavel Fadrus5, Martin Smrcka5, Andrej Besse2, Jana Nekvindova6, Marketa Hermanova7, Radim Jancalek8, Marek Svoboda3, Marian Hajduch9, Pavel Slampa10, Rostislav Vyzula3, Ondrej Slaby11.
Abstract
Glioblastoma multiforme (GBM) is the most malignant primary brain tumor. The prognosis of GBM patients varies considerably and the histopathological examination is not sufficient for individual risk estimation. MicroRNAs (miRNAs) are small, non-coding RNAs that function as post-transcriptional regulators of gene expression and were repeatedly proved to play important roles in pathogenesis of GBM. In our study, we performed global miRNA expression profiling of 58 glioblastoma tissue samples obtained during surgical resections and 10 non-tumor brain tissues. The subsequent analysis revealed 28 significantly deregulated miRNAs in GBM tissue, which were able to precisely classify all examined samples. Correlation with clinical data led to identification of six-miRNA signature significantly associated with progression free survival [hazard ratio (HR) 1.98, 95% confidence interval (CI) 1.33-2.94, P < 0.001] and overa+ll survival (HR 2.86, 95% CI 1.91-4.29, P < 0.001). O(6)-methylguanine-DNA methyltransferase methylation status was evaluated as reference method and Risk Score based on six-miRNA signature indicated significant superiority in prediction of clinical outcome in GBM patients. Multivariate Cox analysis indicated that the Risk Score based on six-miRNA signature is an independent prognostic classifier of GBM patients. We suggest that the Risk Score presents promising prognostic algorithm with potential for individualized treatment decisions in clinical management of GBM patients.Entities:
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Year: 2014 PMID: 25322872 DOI: 10.1093/carcin/bgu212
Source DB: PubMed Journal: Carcinogenesis ISSN: 0143-3334 Impact factor: 4.944