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Identification and validation of potential novel prognostic biomarkers for patients with glioma based on a gene co-expression network

BACKGROUND: Glioma is widely regarded as one of most lethal and challenging diseases of the nervous system. The aim of this study was to identify novel biomarkers that offer better prognosis prediction for Chinese patients with glioma. METHODS: By using systematic approaches, the co-expression modul...

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Autores principales: Jiang, Yan-Wei, Wang, Rui, Zhuang, Yuan-Dong, Chen, Chun-Mei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: AME Publishing Company 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8798165/
https://www.ncbi.nlm.nih.gov/pubmed/35117252
http://dx.doi.org/10.21037/tcr-20-492
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author Jiang, Yan-Wei
Wang, Rui
Zhuang, Yuan-Dong
Chen, Chun-Mei
author_facet Jiang, Yan-Wei
Wang, Rui
Zhuang, Yuan-Dong
Chen, Chun-Mei
author_sort Jiang, Yan-Wei
collection PubMed
description BACKGROUND: Glioma is widely regarded as one of most lethal and challenging diseases of the nervous system. The aim of this study was to identify novel biomarkers that offer better prognosis prediction for Chinese patients with glioma. METHODS: By using systematic approaches, the co-expression modules were identified from the Chinese Glioma Genome Atlas (CGGA) database through weighted gene co-expression network analysis and functional enrichment of essential modules of Kyoto Encyclopedia of Genes and Genomes terms. The co-expression modules were validated using The Cancer Genome Atlas database and the protein-protein interaction (PPI) network. RESULTS: For network construction, 5,374 among 21,494 genes were selected, and an increasing genetic variance was associated with the prognosis of glioma. By using functional enrichment analysis, the involvement of multiple vital processes, including metabolism of fatty acids, was correlated with the patient prognosis. Notably, five hub genes (KCNB1, UST, SOX8, KLHL42, and HDAC4) were identified for these processes. Accordingly, using the Kaplan-Meier method, there was enhanced expression of these genes in patients with significantly lower overall survival rates, especially those from the CGGA database. CONCLUSIONS: This study not only revealed the essential co-expression gene modules in patients with glioma, but it also unraveled the potential signaling pathways underlying these functional processes.
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spelling pubmed-87981652022-02-02 Identification and validation of potential novel prognostic biomarkers for patients with glioma based on a gene co-expression network Jiang, Yan-Wei Wang, Rui Zhuang, Yuan-Dong Chen, Chun-Mei Transl Cancer Res Original Article BACKGROUND: Glioma is widely regarded as one of most lethal and challenging diseases of the nervous system. The aim of this study was to identify novel biomarkers that offer better prognosis prediction for Chinese patients with glioma. METHODS: By using systematic approaches, the co-expression modules were identified from the Chinese Glioma Genome Atlas (CGGA) database through weighted gene co-expression network analysis and functional enrichment of essential modules of Kyoto Encyclopedia of Genes and Genomes terms. The co-expression modules were validated using The Cancer Genome Atlas database and the protein-protein interaction (PPI) network. RESULTS: For network construction, 5,374 among 21,494 genes were selected, and an increasing genetic variance was associated with the prognosis of glioma. By using functional enrichment analysis, the involvement of multiple vital processes, including metabolism of fatty acids, was correlated with the patient prognosis. Notably, five hub genes (KCNB1, UST, SOX8, KLHL42, and HDAC4) were identified for these processes. Accordingly, using the Kaplan-Meier method, there was enhanced expression of these genes in patients with significantly lower overall survival rates, especially those from the CGGA database. CONCLUSIONS: This study not only revealed the essential co-expression gene modules in patients with glioma, but it also unraveled the potential signaling pathways underlying these functional processes. AME Publishing Company 2020-10 /pmc/articles/PMC8798165/ /pubmed/35117252 http://dx.doi.org/10.21037/tcr-20-492 Text en 2020 Translational Cancer Research. All rights reserved. https://creativecommons.org/licenses/by-nc-nd/4.0/Open Access Statement: This is an Open Access article distributed in accordance with the Creative Commons Attribution-NonCommercial-NoDerivs 4.0 International License (CC BY-NC-ND 4.0), which permits the non-commercial replication and distribution of the article with the strict proviso that no changes or edits are made and the original work is properly cited (including links to both the formal publication through the relevant DOI and the license). See: https://creativecommons.org/licenses/by-nc-nd/4.0/.
spellingShingle Original Article
Jiang, Yan-Wei
Wang, Rui
Zhuang, Yuan-Dong
Chen, Chun-Mei
Identification and validation of potential novel prognostic biomarkers for patients with glioma based on a gene co-expression network
title Identification and validation of potential novel prognostic biomarkers for patients with glioma based on a gene co-expression network
title_full Identification and validation of potential novel prognostic biomarkers for patients with glioma based on a gene co-expression network
title_fullStr Identification and validation of potential novel prognostic biomarkers for patients with glioma based on a gene co-expression network
title_full_unstemmed Identification and validation of potential novel prognostic biomarkers for patients with glioma based on a gene co-expression network
title_short Identification and validation of potential novel prognostic biomarkers for patients with glioma based on a gene co-expression network
title_sort identification and validation of potential novel prognostic biomarkers for patients with glioma based on a gene co-expression network
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8798165/
https://www.ncbi.nlm.nih.gov/pubmed/35117252
http://dx.doi.org/10.21037/tcr-20-492
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