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Establishing a glutamine metabolism-based model for predicting the prognosis of low-grade glioma

Background: The natural history of patients with low-grade glioma (LGG) varies widely, but most patients eventually deteriorate, leading to poor prognostic outcomes. We aim to develop biological models that can accurately predict the outcome of LGG prognosis. Methods: Prognostic genes for glutamine...

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Autores principales: Zhang, Mingshi, Li, Mingjun, Liu, Jinrui, Gu, Zhicheng, Lu, Yanmei, Long, Yu, Hou, Yuyi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9723145/
https://www.ncbi.nlm.nih.gov/pubmed/36482907
http://dx.doi.org/10.3389/fgene.2022.1030837
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author Zhang, Mingshi
Li, Mingjun
Liu, Jinrui
Gu, Zhicheng
Lu, Yanmei
Long, Yu
Hou, Yuyi
author_facet Zhang, Mingshi
Li, Mingjun
Liu, Jinrui
Gu, Zhicheng
Lu, Yanmei
Long, Yu
Hou, Yuyi
author_sort Zhang, Mingshi
collection PubMed
description Background: The natural history of patients with low-grade glioma (LGG) varies widely, but most patients eventually deteriorate, leading to poor prognostic outcomes. We aim to develop biological models that can accurately predict the outcome of LGG prognosis. Methods: Prognostic genes for glutamine metabolism were searched by univariate Cox regression, and molecular typing was constructed. Functional enrichment analysis was done to evaluate potential prognostic-related pathways by analyzing differential genes in different subtypes. Enrichment scores of specific gene sets in different subtypes were measured by gene set enrichment analysis. Different immune infiltration levels among subtypes were calculated using algorithms such as CIBERSORT and ESTIMATE. Gene expression levels of prognostic-related gene signatures of glutamine metabolism phenotypes were used to construct a RiskScore model. Receiver operating characteristic curve, decision curve and calibration curve analyses were used to evaluate the reliability and validity of the risk model. The decision tree model was used to determine the best predictor variable ultimately. Results: We found that C1 had the worst prognosis and the highest level of immune infiltration, among which the highest macrophage infiltration can be found in the M2 stage. Moreover, most of the pathways associated with tumor development, such as MYC_TARGETS_V1 and EPITHELIAL_MESENCHYMAL_TRANSITION, were significantly enriched in C1. The wild-type IDH and MGMT hypermethylation were the most abundant in C1. A five-gene risk model related to glutamine metabolism phenotype was established with good performance in both training and validation datasets. The final decision tree demonstrated the RiskScore model as the most significant predictor of prognostic outcomes in individuals with LGG. Conclusion: The RiskScore model related to glutamine metabolism can be an exceedingly accurate predictor for LGG patients, providing valuable suggestions for personalized treatment.
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spelling pubmed-97231452022-12-07 Establishing a glutamine metabolism-based model for predicting the prognosis of low-grade glioma Zhang, Mingshi Li, Mingjun Liu, Jinrui Gu, Zhicheng Lu, Yanmei Long, Yu Hou, Yuyi Front Genet Genetics Background: The natural history of patients with low-grade glioma (LGG) varies widely, but most patients eventually deteriorate, leading to poor prognostic outcomes. We aim to develop biological models that can accurately predict the outcome of LGG prognosis. Methods: Prognostic genes for glutamine metabolism were searched by univariate Cox regression, and molecular typing was constructed. Functional enrichment analysis was done to evaluate potential prognostic-related pathways by analyzing differential genes in different subtypes. Enrichment scores of specific gene sets in different subtypes were measured by gene set enrichment analysis. Different immune infiltration levels among subtypes were calculated using algorithms such as CIBERSORT and ESTIMATE. Gene expression levels of prognostic-related gene signatures of glutamine metabolism phenotypes were used to construct a RiskScore model. Receiver operating characteristic curve, decision curve and calibration curve analyses were used to evaluate the reliability and validity of the risk model. The decision tree model was used to determine the best predictor variable ultimately. Results: We found that C1 had the worst prognosis and the highest level of immune infiltration, among which the highest macrophage infiltration can be found in the M2 stage. Moreover, most of the pathways associated with tumor development, such as MYC_TARGETS_V1 and EPITHELIAL_MESENCHYMAL_TRANSITION, were significantly enriched in C1. The wild-type IDH and MGMT hypermethylation were the most abundant in C1. A five-gene risk model related to glutamine metabolism phenotype was established with good performance in both training and validation datasets. The final decision tree demonstrated the RiskScore model as the most significant predictor of prognostic outcomes in individuals with LGG. Conclusion: The RiskScore model related to glutamine metabolism can be an exceedingly accurate predictor for LGG patients, providing valuable suggestions for personalized treatment. Frontiers Media S.A. 2022-11-22 /pmc/articles/PMC9723145/ /pubmed/36482907 http://dx.doi.org/10.3389/fgene.2022.1030837 Text en Copyright © 2022 Zhang, Li, Liu, Gu, Lu, Long and Hou. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Genetics
Zhang, Mingshi
Li, Mingjun
Liu, Jinrui
Gu, Zhicheng
Lu, Yanmei
Long, Yu
Hou, Yuyi
Establishing a glutamine metabolism-based model for predicting the prognosis of low-grade glioma
title Establishing a glutamine metabolism-based model for predicting the prognosis of low-grade glioma
title_full Establishing a glutamine metabolism-based model for predicting the prognosis of low-grade glioma
title_fullStr Establishing a glutamine metabolism-based model for predicting the prognosis of low-grade glioma
title_full_unstemmed Establishing a glutamine metabolism-based model for predicting the prognosis of low-grade glioma
title_short Establishing a glutamine metabolism-based model for predicting the prognosis of low-grade glioma
title_sort establishing a glutamine metabolism-based model for predicting the prognosis of low-grade glioma
topic Genetics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9723145/
https://www.ncbi.nlm.nih.gov/pubmed/36482907
http://dx.doi.org/10.3389/fgene.2022.1030837
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