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Glioblastoma cell differentiation trajectory predicts the immunotherapy response and overall survival of patients

Glioblastoma (GBM) is the most common and lethal primary brain tumor. In this study, we aimed to investigate the differentiation states of GBM cells and their clinical relevance. Integrated single-cell RNA-sequencing (scRNA-seq) data and bulk RNA-seq data from GBM samples were used for analysis. Two...

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Autores principales: Wang, Zihao, Guo, Xiaopeng, Gao, Lu, Wang, Yu, Ma, Wenbin, Xing, Bing
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7585071/
https://www.ncbi.nlm.nih.gov/pubmed/32957084
http://dx.doi.org/10.18632/aging.103695
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author Wang, Zihao
Guo, Xiaopeng
Gao, Lu
Wang, Yu
Ma, Wenbin
Xing, Bing
author_facet Wang, Zihao
Guo, Xiaopeng
Gao, Lu
Wang, Yu
Ma, Wenbin
Xing, Bing
author_sort Wang, Zihao
collection PubMed
description Glioblastoma (GBM) is the most common and lethal primary brain tumor. In this study, we aimed to investigate the differentiation states of GBM cells and their clinical relevance. Integrated single-cell RNA-sequencing (scRNA-seq) data and bulk RNA-seq data from GBM samples were used for analysis. Two subsets of GBM cells in distinct differentiation states were characterized, and 498 GBM cell differentiation-related genes (GDRGs) were identified. GDRGs were significantly correlated with immune regulation and metabolic pathways. We classified the GBM patients into two groups based on the expression of GDRGs in tumors and found that the cell differentiation-based classification successfully predicted patient overall survival (OS), immune checkpoint expression and likelihood of immunotherapy response in GBMs. FN1, APOE, RPL7A and GSTM2 were the 4 most significant survival-predicting GDRGs, and patients with different expression levels of each of these genes had distinct survival outcomes. Finally, a nomogram composed of the GDRG signature, age, pharmacotherapy, radiotherapy, IDH mutations and MGMT promoter methylation was generated and validated in two large GBM cohorts to predict GBM prognosis. This study highlights the significant roles of cell differentiation in predicting the clinical outcomes of GBM patients and their potential response to immunotherapy, suggesting promising therapeutic targets for GBM.
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spelling pubmed-75850712020-11-03 Glioblastoma cell differentiation trajectory predicts the immunotherapy response and overall survival of patients Wang, Zihao Guo, Xiaopeng Gao, Lu Wang, Yu Ma, Wenbin Xing, Bing Aging (Albany NY) Research Paper Glioblastoma (GBM) is the most common and lethal primary brain tumor. In this study, we aimed to investigate the differentiation states of GBM cells and their clinical relevance. Integrated single-cell RNA-sequencing (scRNA-seq) data and bulk RNA-seq data from GBM samples were used for analysis. Two subsets of GBM cells in distinct differentiation states were characterized, and 498 GBM cell differentiation-related genes (GDRGs) were identified. GDRGs were significantly correlated with immune regulation and metabolic pathways. We classified the GBM patients into two groups based on the expression of GDRGs in tumors and found that the cell differentiation-based classification successfully predicted patient overall survival (OS), immune checkpoint expression and likelihood of immunotherapy response in GBMs. FN1, APOE, RPL7A and GSTM2 were the 4 most significant survival-predicting GDRGs, and patients with different expression levels of each of these genes had distinct survival outcomes. Finally, a nomogram composed of the GDRG signature, age, pharmacotherapy, radiotherapy, IDH mutations and MGMT promoter methylation was generated and validated in two large GBM cohorts to predict GBM prognosis. This study highlights the significant roles of cell differentiation in predicting the clinical outcomes of GBM patients and their potential response to immunotherapy, suggesting promising therapeutic targets for GBM. Impact Journals 2020-09-21 /pmc/articles/PMC7585071/ /pubmed/32957084 http://dx.doi.org/10.18632/aging.103695 Text en Copyright: © 2020 Wang et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/3.0/) (CC BY 3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Paper
Wang, Zihao
Guo, Xiaopeng
Gao, Lu
Wang, Yu
Ma, Wenbin
Xing, Bing
Glioblastoma cell differentiation trajectory predicts the immunotherapy response and overall survival of patients
title Glioblastoma cell differentiation trajectory predicts the immunotherapy response and overall survival of patients
title_full Glioblastoma cell differentiation trajectory predicts the immunotherapy response and overall survival of patients
title_fullStr Glioblastoma cell differentiation trajectory predicts the immunotherapy response and overall survival of patients
title_full_unstemmed Glioblastoma cell differentiation trajectory predicts the immunotherapy response and overall survival of patients
title_short Glioblastoma cell differentiation trajectory predicts the immunotherapy response and overall survival of patients
title_sort glioblastoma cell differentiation trajectory predicts the immunotherapy response and overall survival of patients
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7585071/
https://www.ncbi.nlm.nih.gov/pubmed/32957084
http://dx.doi.org/10.18632/aging.103695
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