Cargando…

Gut Microbiome Alterations Affect Glioma Development and Foxp3 Expression in Tumor Microenvironment in Mice

Glioma is the most common malignant tumor of the central nervous system (CNS), with high degree of malignancy and poor prognosis. The gut microbiome (GM) is composed of microorganisms with different properties and functions, which play an important role in human physiology and biological activities....

Descripción completa

Detalles Bibliográficos
Autores principales: Fan, Yiqi, Su, Qing, Chen, Junxiao, Wang, Yong, He, Shuai
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8957261/
https://www.ncbi.nlm.nih.gov/pubmed/35345443
http://dx.doi.org/10.3389/fonc.2022.836953
_version_ 1784676729352093696
author Fan, Yiqi
Su, Qing
Chen, Junxiao
Wang, Yong
He, Shuai
author_facet Fan, Yiqi
Su, Qing
Chen, Junxiao
Wang, Yong
He, Shuai
author_sort Fan, Yiqi
collection PubMed
description Glioma is the most common malignant tumor of the central nervous system (CNS), with high degree of malignancy and poor prognosis. The gut microbiome (GM) is composed of microorganisms with different properties and functions, which play an important role in human physiology and biological activities. It has been proved that GM can affect the development of glioma through natural immunity, but whether GM can affect glioma through adaptive immunity and whether there are some microorganisms in the GM that may affect glioma growth still remain unclear. In our study, we evaluated the relationship between GM and glioma. We proved that (I) glioma growth can induce structural changes of mouse GM, including the decreased abundance of Bacteroidia and increased abundance of Firmicutes. (II) GM dysbiosis can downregulate Foxp3 expression in the brain and promote glioma growth. A balanced environment of GM can upregulate the expression of Foxp3 in the brain and delay the development of glioma. (III) The increased abundance of Bacteroidia is associated with accelerated glioma progression, while its decreased abundance is associated with delayed glioma progression, which may be one of the key microorganisms affecting glioma growth. This study is helpful to reveal the relationship between GM and glioma development and provide new ideas for adjuvant therapy of glioma.
format Online
Article
Text
id pubmed-8957261
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher Frontiers Media S.A.
record_format MEDLINE/PubMed
spelling pubmed-89572612022-03-27 Gut Microbiome Alterations Affect Glioma Development and Foxp3 Expression in Tumor Microenvironment in Mice Fan, Yiqi Su, Qing Chen, Junxiao Wang, Yong He, Shuai Front Oncol Oncology Glioma is the most common malignant tumor of the central nervous system (CNS), with high degree of malignancy and poor prognosis. The gut microbiome (GM) is composed of microorganisms with different properties and functions, which play an important role in human physiology and biological activities. It has been proved that GM can affect the development of glioma through natural immunity, but whether GM can affect glioma through adaptive immunity and whether there are some microorganisms in the GM that may affect glioma growth still remain unclear. In our study, we evaluated the relationship between GM and glioma. We proved that (I) glioma growth can induce structural changes of mouse GM, including the decreased abundance of Bacteroidia and increased abundance of Firmicutes. (II) GM dysbiosis can downregulate Foxp3 expression in the brain and promote glioma growth. A balanced environment of GM can upregulate the expression of Foxp3 in the brain and delay the development of glioma. (III) The increased abundance of Bacteroidia is associated with accelerated glioma progression, while its decreased abundance is associated with delayed glioma progression, which may be one of the key microorganisms affecting glioma growth. This study is helpful to reveal the relationship between GM and glioma development and provide new ideas for adjuvant therapy of glioma. Frontiers Media S.A. 2022-03-08 /pmc/articles/PMC8957261/ /pubmed/35345443 http://dx.doi.org/10.3389/fonc.2022.836953 Text en Copyright © 2022 Fan, Su, Chen, Wang and He 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 Oncology
Fan, Yiqi
Su, Qing
Chen, Junxiao
Wang, Yong
He, Shuai
Gut Microbiome Alterations Affect Glioma Development and Foxp3 Expression in Tumor Microenvironment in Mice
title Gut Microbiome Alterations Affect Glioma Development and Foxp3 Expression in Tumor Microenvironment in Mice
title_full Gut Microbiome Alterations Affect Glioma Development and Foxp3 Expression in Tumor Microenvironment in Mice
title_fullStr Gut Microbiome Alterations Affect Glioma Development and Foxp3 Expression in Tumor Microenvironment in Mice
title_full_unstemmed Gut Microbiome Alterations Affect Glioma Development and Foxp3 Expression in Tumor Microenvironment in Mice
title_short Gut Microbiome Alterations Affect Glioma Development and Foxp3 Expression in Tumor Microenvironment in Mice
title_sort gut microbiome alterations affect glioma development and foxp3 expression in tumor microenvironment in mice
topic Oncology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8957261/
https://www.ncbi.nlm.nih.gov/pubmed/35345443
http://dx.doi.org/10.3389/fonc.2022.836953
work_keys_str_mv AT fanyiqi gutmicrobiomealterationsaffectgliomadevelopmentandfoxp3expressionintumormicroenvironmentinmice
AT suqing gutmicrobiomealterationsaffectgliomadevelopmentandfoxp3expressionintumormicroenvironmentinmice
AT chenjunxiao gutmicrobiomealterationsaffectgliomadevelopmentandfoxp3expressionintumormicroenvironmentinmice
AT wangyong gutmicrobiomealterationsaffectgliomadevelopmentandfoxp3expressionintumormicroenvironmentinmice
AT heshuai gutmicrobiomealterationsaffectgliomadevelopmentandfoxp3expressionintumormicroenvironmentinmice