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A prognostic signature based on three non‐coding RNA s for prediction of the overall survival of glioma patients
Recent studies have identified certain non‐coding RNA s (nc RNA s) as biomarkers of disease progression. Glioma is the most common primary intracranial cancer, with high mortality. Here, we developed a prognostic signature for prediction of overall survival (OS) of glioma patients by analyzing nc RN...
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Published in: | FEBS open bio 2019-04, Vol.9 (4), p.682-692 |
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Main Authors: | , , , , , |
Format: | Article |
Language: | English |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | Recent studies have identified certain non‐coding
RNA
s (nc
RNA
s) as biomarkers of disease progression. Glioma is the most common primary intracranial cancer, with high mortality. Here, we developed a prognostic signature for prediction of overall survival (OS) of glioma patients by analyzing nc
RNA
expression profiles. We downloaded gene expression profiles of glioma patients along with their clinical information from the Gene Expression Omnibus and extracted nc
RNA
expression profiles via a microarray annotation file. Correlations between nc
RNA
s and glioma patients’
OS
were first evaluated through univariate Cox regression analysis and a permutation test, followed by random survival forest analysis for further screening of valuable nc
RNA
signatures. Prognostic signatures could be established as a risk score formula by including nc
RNA
signature expression values weighted by their estimated regression coefficients. Patients could be divided into high risk and low risk subgroups by using the median risk score as cutoff. As a result, glioma patients with a high risk score tended to have shorter
OS
than those with low risk scores, which was confirmed by analyzing another set of glioma patients in an independent dataset. Additionally, gene set enrichment analysis showed significant enrichment of cancer development‐related biological processes and pathways. Our study may provide further insights into the evaluation of glioma patients’ prognosis. |
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ISSN: | 2211-5463 2211-5463 |
DOI: | 10.1002/2211-5463.12602 |