Cargando…
Single-Cell Transcriptome Profiling Signatures and Alterations of Microglia Associated With Glioblastoma Associate Microglia Contribution to Tumor Formation
Glioblastoma (GBM), which occasionally occurs in pediatric patients, is the most common tumor of the central nervous system in adults. Clinically, GBM is classified as low-grade to high-grade (from 1 to 4) and is characterized by late discovery, limited effective treatment methods, and poor efficacy...
Autores principales: | , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9176381/ https://www.ncbi.nlm.nih.gov/pubmed/35693633 http://dx.doi.org/10.3389/pore.2022.1610067 |
_version_ | 1784722652372402176 |
---|---|
author | Xia, Hailong Deng, Lei Meng, Shu Liu, Xipeng Zheng, Chao |
author_facet | Xia, Hailong Deng, Lei Meng, Shu Liu, Xipeng Zheng, Chao |
author_sort | Xia, Hailong |
collection | PubMed |
description | Glioblastoma (GBM), which occasionally occurs in pediatric patients, is the most common tumor of the central nervous system in adults. Clinically, GBM is classified as low-grade to high-grade (from 1 to 4) and is characterized by late discovery, limited effective treatment methods, and poor efficacy. With the development of immunotherapy technology, effective GBM treatment strategies are of great significance. The main immune cells found in the GBM tumor microenvironment are macrophages and microglia (MG). Both these monocytes play important roles in the occurrence and development of GBM. Macrophages are recruited during tumorigenesis, whereas MG is present in the brain during embryonic development. Interestingly, the accumulation of these monocytes is inversely proportional to the survival of adult GBM patients but not the pediatric GBM patients. This study used single-cell RNA-seq data to reveal the heterogeneity of MG in tumor lesions and to explore the role of different MG subtypes in the occurrence and development of GBM. The results may help find new targets for immunotherapy of GBM. |
format | Online Article Text |
id | pubmed-9176381 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-91763812022-06-09 Single-Cell Transcriptome Profiling Signatures and Alterations of Microglia Associated With Glioblastoma Associate Microglia Contribution to Tumor Formation Xia, Hailong Deng, Lei Meng, Shu Liu, Xipeng Zheng, Chao Pathol Oncol Res Pathology and Oncology Archive Glioblastoma (GBM), which occasionally occurs in pediatric patients, is the most common tumor of the central nervous system in adults. Clinically, GBM is classified as low-grade to high-grade (from 1 to 4) and is characterized by late discovery, limited effective treatment methods, and poor efficacy. With the development of immunotherapy technology, effective GBM treatment strategies are of great significance. The main immune cells found in the GBM tumor microenvironment are macrophages and microglia (MG). Both these monocytes play important roles in the occurrence and development of GBM. Macrophages are recruited during tumorigenesis, whereas MG is present in the brain during embryonic development. Interestingly, the accumulation of these monocytes is inversely proportional to the survival of adult GBM patients but not the pediatric GBM patients. This study used single-cell RNA-seq data to reveal the heterogeneity of MG in tumor lesions and to explore the role of different MG subtypes in the occurrence and development of GBM. The results may help find new targets for immunotherapy of GBM. Frontiers Media S.A. 2022-05-25 /pmc/articles/PMC9176381/ /pubmed/35693633 http://dx.doi.org/10.3389/pore.2022.1610067 Text en Copyright © 2022 Xia, Deng, Meng, Liu and Zheng. 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 | Pathology and Oncology Archive Xia, Hailong Deng, Lei Meng, Shu Liu, Xipeng Zheng, Chao Single-Cell Transcriptome Profiling Signatures and Alterations of Microglia Associated With Glioblastoma Associate Microglia Contribution to Tumor Formation |
title | Single-Cell Transcriptome Profiling Signatures and Alterations of Microglia Associated With Glioblastoma Associate Microglia Contribution to Tumor Formation |
title_full | Single-Cell Transcriptome Profiling Signatures and Alterations of Microglia Associated With Glioblastoma Associate Microglia Contribution to Tumor Formation |
title_fullStr | Single-Cell Transcriptome Profiling Signatures and Alterations of Microglia Associated With Glioblastoma Associate Microglia Contribution to Tumor Formation |
title_full_unstemmed | Single-Cell Transcriptome Profiling Signatures and Alterations of Microglia Associated With Glioblastoma Associate Microglia Contribution to Tumor Formation |
title_short | Single-Cell Transcriptome Profiling Signatures and Alterations of Microglia Associated With Glioblastoma Associate Microglia Contribution to Tumor Formation |
title_sort | single-cell transcriptome profiling signatures and alterations of microglia associated with glioblastoma associate microglia contribution to tumor formation |
topic | Pathology and Oncology Archive |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9176381/ https://www.ncbi.nlm.nih.gov/pubmed/35693633 http://dx.doi.org/10.3389/pore.2022.1610067 |
work_keys_str_mv | AT xiahailong singlecelltranscriptomeprofilingsignaturesandalterationsofmicrogliaassociatedwithglioblastomaassociatemicrogliacontributiontotumorformation AT denglei singlecelltranscriptomeprofilingsignaturesandalterationsofmicrogliaassociatedwithglioblastomaassociatemicrogliacontributiontotumorformation AT mengshu singlecelltranscriptomeprofilingsignaturesandalterationsofmicrogliaassociatedwithglioblastomaassociatemicrogliacontributiontotumorformation AT liuxipeng singlecelltranscriptomeprofilingsignaturesandalterationsofmicrogliaassociatedwithglioblastomaassociatemicrogliacontributiontotumorformation AT zhengchao singlecelltranscriptomeprofilingsignaturesandalterationsofmicrogliaassociatedwithglioblastomaassociatemicrogliacontributiontotumorformation |