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pmid:31897239

Twenty Metabolic Genes Based Signature Predicts Survival of Glioma Patients.

Wenfang Xu · Zhenhao Liu · He Ren · Xueqing Peng · Aoshen Wu · Duan Ma · Gang Liu · Lei Liu

Journal of Cancer · 2020 doi:10.7150/jca.30923

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title
Twenty Metabolic Genes Based Signature Predicts Survival of Glioma Patients.
doi
10.7150/jca.30923
pmid
31897239
authors array · 8 items
[0]
Wenfang Xu
[1]
Zhenhao Liu
[2]
He Ren
[3]
Xueqing Peng
[4]
Aoshen Wu
[5]
Duan Ma
[6]
Gang Liu
[7]
Lei Liu
journal
Journal of Cancer
year
2020
abstract
Background: Glioma, caused by carcinogenesis of brain and spinal glial cells, is the most common primary malignant brain tumor. To find the important indicator for glioma prognosis is still a challenge and the metabolic alteration of glioma has been frequently reported recently. Methods: In our current work, a risk score model based on the expression of twenty metabolic genes was developed using the metabolic gene expressions in The Cancer Genome Atlas (TCGA) dataset, the methods of which included the cox multivariate regression and the random forest variable hunting, a kind of machine learning algorithm, and the risk score generated from this model is used to make predictions in the survival of glioma patients in the training dataset. Subsequently, the result was further verified in other three verification sets (GSE4271, GSE4412 and GSE16011). Risk score related pathways collected in the Kyoto Encyclopedia of Genes and Genomes (KEGG) database were identified using Gene Set Enrichment Analysis (GSEA). Results: The risk score generated from our model makes good predictions in the survival of glioma patients in the training dataset and other three verification sets. By assessing the relationships between clinical indicators and the risk score, we found that the risk score was an independent and significant indicator for the prognosis of glioma patients. Simultaneously, we conducted a survival analysis of the patients who received chemotherapy and who did not, finding that the risk score was equally valid in both cases. And signaling pathways related to the genesis and development of multiple cancers were also identified. Conclusions: In summary, our risk score model is predictive for 967 glioma patients' survival from four independent datasets, and the risk score is a meaningful and independent parameter of the clinicopathological information.
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title
Intrinsic Gene Expression Profiles of Gliomas are a Better Predictor of Survival than Histology
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Molecular subclasses of high-grade glioma: prognosis, disease progression, and neurogenesis
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2026-11-01T15:39:54Z
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All data generated or analyzed during this study are included in published article. It is available TCGA Xena website (https://tcga.xenahubs.net/) and GEO (https://www.ncbi.nlm.nih.gov/geo/) with the following accession numbers: GSE4271, GSE4412, GSE16011.
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The paper names GSE4271, GSE4412, GSE16011 in Gene Expression Omnibus (GEO) and the accession resolves in the repository. No dataset was downloaded and no licence was read.
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Complete file
{"sci_version": "1.2", "schema": "https://corpus.bntrg.co.uk/sci/1.0/sci.schema.json", "id": "pmid:31897239", "kind": "science-record", "revision": 4, "content_hash": "sha256:3035ba1f98ccd8cf4167f8350b3e1551c13d9bdf28752f8443c0ca9de5e8d9ea", "created_at": "2026-11-01T15:40:54Z", "updated_at": "2026-11-01T22:01:10Z", "generator": {"name": "corpus-assay-engine", "run_id": "reading-sci-2026-11-01"}, "paper": {"state": "complete", "title": "Twenty Metabolic Genes Based Signature Predicts Survival of Glioma Patients.", "doi": "10.7150/jca.30923", "pmid": "31897239", "authors": ["Wenfang Xu", "Zhenhao Liu", "He Ren", "Xueqing Peng", "Aoshen Wu", "Duan Ma", "Gang Liu", "Lei Liu"], "journal": "Journal of Cancer", "year": 2020, "abstract": "Background: Glioma, caused by carcinogenesis of brain and spinal glial cells, is the most common primary malignant brain tumor. To find the important indicator for glioma prognosis is still a challenge and the metabolic alteration of glioma has been frequently reported recently. Methods: In our current work, a risk score model based on the expression of twenty metabolic genes was developed using the metabolic gene expressions in The Cancer Genome Atlas (TCGA) dataset, the methods of which included the cox multivariate regression and the random forest variable hunting, a kind of machine learning algorithm, and the risk score generated from this model is used to make predictions in the survival of glioma patients in the training dataset. Subsequently, the result was further verified in other three verification sets (GSE4271, GSE4412 and GSE16011). Risk score related pathways collected in the Kyoto Encyclopedia of Genes and Genomes (KEGG) database were identified using Gene Set Enrichment Analysis (GSEA). Results: The risk score generated from our model makes good predictions in the survival of glioma patients in the training dataset and other three verification sets. By assessing the relationships between clinical indicators and the risk score, we found that the risk score was an independent and significant indicator for the prognosis of glioma patients. Simultaneously, we conducted a survival analysis of the patients who received chemotherapy and who did not, finding that the risk score was equally valid in both cases. And signaling pathways related to the genesis and development of multiple cancers were also identified. Conclusions: In summary, our risk score model is predictive for 967 glioma patients' survival from four independent datasets, and the risk score is a meaningful and independent parameter of the clinicopathological information.", "claims": [{"id": "claim-data-access", "statement": "All data generated or analyzed during this study are included in published article. It is available TCGA Xena website (https://tcga.xenahubs.net/) and GEO (https://www.ncbi.nlm.nih.gov/geo/) with the following accession numbers: GSE4271, GSE4412, GSE16011.", "kind": "methodological", "target": null, "evidence": [{"asset": "source:pmid:31897239", "locator": "sections[16] \"ack\" paragraph 1", "quote": "All data generated or analyzed during this study are included in published article. 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