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pmid:23502430
Identification of prognostic gene signatures of glioblastoma: a study based on TCGA data analysis.
Yong-Wan Kim · Dimpy Koul · Se Hoon Kim · Agda Karina Lucio-Eterovic · Pablo R Freire · Jun Yao · Jing Wang · Jonas S Almeida · Ken Aldape · W K Alfred Yung
Neuro-oncology · 2013 doi:10.1093/neuonc/not024
Paper
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Experiment
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Data
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Analysis
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Execution
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Complete file
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Kaplan-Meier plots showed that the median survival of group 3 was markedly longer (127 weeks) than that of groups 1 and 2 (47 and 52 weeks, respectively). We then validated the 42 probe sets to stratify the patients according to survival in other public GBM gene expression datasets (eg, GSE4290 dataset). An overall analysis of the gene expression and copy number aberration using a multivariate Cox regression model showed that the 42 probe sets had a significant (P < .018) prognostic value independent of other variables.\nCONCLUSIONS: By integrating multidimensional genomic data from TCGA, we identified a specific survival model in a new prognostic group of GBM and suggest that molecular stratification of patients with GBM into homogeneous subgroups may provide opportunities for the development of new treatment modalities.", "claims": [{"id": "claim-target-result", "statement": "Using multivariate Cox regression on integrated TCGA gene-expression and copy-number aberration data, the 42-probe-set survival model significantly stratified GBM patients into three prognostic groups, was validated in other public GBM gene-expression datasets, and retained independent prognostic value (P < .018).", "kind": "qualitative", "target": null, "evidence": [{"asset": "source:pmid:23502430", "locator": "sections[0] \"Abstract\" paragraph 3", "quote": "We then validated the 42 probe sets to stratify the patients according to survival in other public GBM gene expression datasets (eg, GSE4290 dataset)."}, {"asset": "source:pmid:23502430", "locator": "sections[0] \"Abstract\" paragraph 3", "quote": "An overall analysis of the gene expression and copy number aberration using a multivariate Cox regression model showed that the 42 probe sets had a significant (P < .018) prognostic value independent of other variables."}], "state": "complete"}], "gaps": []}, "experiment": {"state": "partial", "objective": "Using multivariate Cox regression on integrated TCGA gene-expression and copy-number aberration data, the 42-probe-set survival model significantly stratified GBM patients into three prognostic groups, was validated in other public GBM gene-expression datasets, and retained independent prognostic value (P < .018).", "steps": [{"id": "read_published_estimate", "order": 1, "name": "Read the published estimate from the source", "kind": "other", "state": "complete", "blocked_on": null, "description": "The claim, method and evidence span published with the source article.", "duration_hours": null, "parameters": {}, "inputs": ["source:pmid:23502430"], "outputs": ["the published estimate and its evidence"], "instruments": [], "reagents": []}, {"id": "obtain_source_data", "order": 2, "name": "Obtain the source data from the named repository", "kind": "data-preparation", "state": "blocked", "blocked_on": "data:accession_absent", "description": "The GEO series accession resolves and its sample accessions are listed. 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