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In silico identification of the prognostic biomarkers and therapeutic targets associated with cancer stem cell characteristics of glioma

Glioma is the common histological subtype of malignancy in central nervous system, with a high morbidity and mortality. Cancer stem cells (CSCs) play an important role in regulating the tumorigenesis and progression of glioma; however, the prognostic biomarkers and therapeutic targets associated wit...

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Autores principales: Lvu, Wen, Fei, Xu, Chen, Cheng, Zhang, Bo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Portland Press Ltd. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7418212/
https://www.ncbi.nlm.nih.gov/pubmed/32725165
http://dx.doi.org/10.1042/BSR20201037
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author Lvu, Wen
Fei, Xu
Chen, Cheng
Zhang, Bo
author_facet Lvu, Wen
Fei, Xu
Chen, Cheng
Zhang, Bo
author_sort Lvu, Wen
collection PubMed
description Glioma is the common histological subtype of malignancy in central nervous system, with a high morbidity and mortality. Cancer stem cells (CSCs) play an important role in regulating the tumorigenesis and progression of glioma; however, the prognostic biomarkers and therapeutic targets associated with CSC characteristics have not been fully acknowledged in glioma. In order to identify the prognostic stemness-related genes (SRGs) of glioma in silico, the RNA sequencing data of patients with glioma were retrieved from The Cancer Genome Atlas (TCGA) databases. The mRNA expression-based stemness index (mRNAsi) was significantly associated with the glioma histologic grade, isocitrate dehydrogenase 1 (IDH1) mutation and overall survival of glioma patients by the nonparametric test and Kaplan–Meier survival analysis. A total of 340 SRGs were identified as the overlapped stemness-related differential expressed genes (DEGs) of different histologic grade screened by the univariate Cox analysis. Based on 11 prognostic SRGs, the predict nomogram was constructed with the AUC of 0.832. Moreover, the risk score of the nomogram was an independent prognostic factor, indicating its significant applicability. Besides other eight reported biomarkers of glioma, we found that F2RL2, CLCNKA and LOXL4 were first identified as prognostic biomarkers for glioma. In conclusion, this bioinformatics study demonstrates the mRNAsi as a reliable index for the IDH1 mutation, histologic grade and OS of glioma patients and provides a well-applied model for predicting the OS for patients with glioma based on prognostic SRGs. Additionally, this in silico study also identifies three novel prognostic biomarkers (F2RL2, CLCNKA and LOXL4) for glioma patients.
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spelling pubmed-74182122020-08-19 In silico identification of the prognostic biomarkers and therapeutic targets associated with cancer stem cell characteristics of glioma Lvu, Wen Fei, Xu Chen, Cheng Zhang, Bo Biosci Rep Cancer Glioma is the common histological subtype of malignancy in central nervous system, with a high morbidity and mortality. Cancer stem cells (CSCs) play an important role in regulating the tumorigenesis and progression of glioma; however, the prognostic biomarkers and therapeutic targets associated with CSC characteristics have not been fully acknowledged in glioma. In order to identify the prognostic stemness-related genes (SRGs) of glioma in silico, the RNA sequencing data of patients with glioma were retrieved from The Cancer Genome Atlas (TCGA) databases. The mRNA expression-based stemness index (mRNAsi) was significantly associated with the glioma histologic grade, isocitrate dehydrogenase 1 (IDH1) mutation and overall survival of glioma patients by the nonparametric test and Kaplan–Meier survival analysis. A total of 340 SRGs were identified as the overlapped stemness-related differential expressed genes (DEGs) of different histologic grade screened by the univariate Cox analysis. Based on 11 prognostic SRGs, the predict nomogram was constructed with the AUC of 0.832. Moreover, the risk score of the nomogram was an independent prognostic factor, indicating its significant applicability. Besides other eight reported biomarkers of glioma, we found that F2RL2, CLCNKA and LOXL4 were first identified as prognostic biomarkers for glioma. In conclusion, this bioinformatics study demonstrates the mRNAsi as a reliable index for the IDH1 mutation, histologic grade and OS of glioma patients and provides a well-applied model for predicting the OS for patients with glioma based on prognostic SRGs. Additionally, this in silico study also identifies three novel prognostic biomarkers (F2RL2, CLCNKA and LOXL4) for glioma patients. Portland Press Ltd. 2020-08-10 /pmc/articles/PMC7418212/ /pubmed/32725165 http://dx.doi.org/10.1042/BSR20201037 Text en © 2020 The Author(s). https://creativecommons.org/licenses/by/4.0/ This is an open access article published by Portland Press Limited on behalf of the Biochemical Society and distributed under the Creative Commons Attribution License 4.0 (CC BY).
spellingShingle Cancer
Lvu, Wen
Fei, Xu
Chen, Cheng
Zhang, Bo
In silico identification of the prognostic biomarkers and therapeutic targets associated with cancer stem cell characteristics of glioma
title In silico identification of the prognostic biomarkers and therapeutic targets associated with cancer stem cell characteristics of glioma
title_full In silico identification of the prognostic biomarkers and therapeutic targets associated with cancer stem cell characteristics of glioma
title_fullStr In silico identification of the prognostic biomarkers and therapeutic targets associated with cancer stem cell characteristics of glioma
title_full_unstemmed In silico identification of the prognostic biomarkers and therapeutic targets associated with cancer stem cell characteristics of glioma
title_short In silico identification of the prognostic biomarkers and therapeutic targets associated with cancer stem cell characteristics of glioma
title_sort in silico identification of the prognostic biomarkers and therapeutic targets associated with cancer stem cell characteristics of glioma
topic Cancer
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7418212/
https://www.ncbi.nlm.nih.gov/pubmed/32725165
http://dx.doi.org/10.1042/BSR20201037
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