Immunological classification of gliomas based on immunogenomic profiling

Abstract Background Gliomas are heterogeneous in the tumor immune microenvironment (TIM). However, a classification of gliomas based on immunogenomic profiling remains lacking. Methods We hierarchically clustered gliomas based on the enrichment levels of 28 immune cells in the TIM in five datasets a...

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Main Authors: Qiushi Feng, Lin Li, Mengyuan Li, Xiaosheng Wang
Format: Article
Language:English
Published: BMC 2020-11-01
Series:Journal of Neuroinflammation
Subjects:
Online Access:https://doi.org/10.1186/s12974-020-02030-w
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spelling doaj-2d80d9ebb3d14c4586a465f28418ddfa2020-11-29T12:08:41ZengBMCJournal of Neuroinflammation1742-20942020-11-0117111210.1186/s12974-020-02030-wImmunological classification of gliomas based on immunogenomic profilingQiushi Feng0Lin Li1Mengyuan Li2Xiaosheng Wang3Biomedical Informatics Research Lab, School of Basic Medicine and Clinical Pharmacy, China Pharmaceutical UniversityBiomedical Informatics Research Lab, School of Basic Medicine and Clinical Pharmacy, China Pharmaceutical UniversityBiomedical Informatics Research Lab, School of Basic Medicine and Clinical Pharmacy, China Pharmaceutical UniversityBiomedical Informatics Research Lab, School of Basic Medicine and Clinical Pharmacy, China Pharmaceutical UniversityAbstract Background Gliomas are heterogeneous in the tumor immune microenvironment (TIM). However, a classification of gliomas based on immunogenomic profiling remains lacking. Methods We hierarchically clustered gliomas based on the enrichment levels of 28 immune cells in the TIM in five datasets and obtained three clusters: immunity-high, immunity-medium, and immunity-low. Results Glioblastomas were mainly distributed in immunity-high and immunity-medium, while lower-grade gliomas were distributed in all the three subtypes and predominated in immunity-low. Immunity-low displayed a better survival than other subtypes, indicating a negative correlation between immune infiltration and survival prognosis in gliomas. IDH mutations had a negative correlation with glioma immunity. Immunity-high had higher tumor stemness and epithelial-mesenchymal transition scores and included more high-grade tumors than immunity-low, suggesting that elevated immunity is associated with tumor progression in gliomas. Immunity-high had higher tumor mutation burden and more frequent somatic copy number alterations, suggesting a positive association between tumor immunity and genomic instability in gliomas. Conclusions The identification of immune-specific glioma subtypes has potential clinical implications for the immunotherapy of gliomas.https://doi.org/10.1186/s12974-020-02030-wGliomaLower-grade gliomaGlioblastomaTumor immune microenvironmentImmunological classificationImmunogenomic profiling
collection DOAJ
language English
format Article
sources DOAJ
author Qiushi Feng
Lin Li
Mengyuan Li
Xiaosheng Wang
spellingShingle Qiushi Feng
Lin Li
Mengyuan Li
Xiaosheng Wang
Immunological classification of gliomas based on immunogenomic profiling
Journal of Neuroinflammation
Glioma
Lower-grade glioma
Glioblastoma
Tumor immune microenvironment
Immunological classification
Immunogenomic profiling
author_facet Qiushi Feng
Lin Li
Mengyuan Li
Xiaosheng Wang
author_sort Qiushi Feng
title Immunological classification of gliomas based on immunogenomic profiling
title_short Immunological classification of gliomas based on immunogenomic profiling
title_full Immunological classification of gliomas based on immunogenomic profiling
title_fullStr Immunological classification of gliomas based on immunogenomic profiling
title_full_unstemmed Immunological classification of gliomas based on immunogenomic profiling
title_sort immunological classification of gliomas based on immunogenomic profiling
publisher BMC
series Journal of Neuroinflammation
issn 1742-2094
publishDate 2020-11-01
description Abstract Background Gliomas are heterogeneous in the tumor immune microenvironment (TIM). However, a classification of gliomas based on immunogenomic profiling remains lacking. Methods We hierarchically clustered gliomas based on the enrichment levels of 28 immune cells in the TIM in five datasets and obtained three clusters: immunity-high, immunity-medium, and immunity-low. Results Glioblastomas were mainly distributed in immunity-high and immunity-medium, while lower-grade gliomas were distributed in all the three subtypes and predominated in immunity-low. Immunity-low displayed a better survival than other subtypes, indicating a negative correlation between immune infiltration and survival prognosis in gliomas. IDH mutations had a negative correlation with glioma immunity. Immunity-high had higher tumor stemness and epithelial-mesenchymal transition scores and included more high-grade tumors than immunity-low, suggesting that elevated immunity is associated with tumor progression in gliomas. Immunity-high had higher tumor mutation burden and more frequent somatic copy number alterations, suggesting a positive association between tumor immunity and genomic instability in gliomas. Conclusions The identification of immune-specific glioma subtypes has potential clinical implications for the immunotherapy of gliomas.
topic Glioma
Lower-grade glioma
Glioblastoma
Tumor immune microenvironment
Immunological classification
Immunogenomic profiling
url https://doi.org/10.1186/s12974-020-02030-w
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AT linli immunologicalclassificationofgliomasbasedonimmunogenomicprofiling
AT mengyuanli immunologicalclassificationofgliomasbasedonimmunogenomicprofiling
AT xiaoshengwang immunologicalclassificationofgliomasbasedonimmunogenomicprofiling
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