Mitochondrial Dysfunction, Macrophage, and Microglia in Brain Cancer

Glioblastoma (GBM) is the most common malignant brain cancer. Increasing evidence suggests that mitochondrial dysfunction plays a key role in GBM progression as mitochondria is essential in regulating cell metabolism, oxidative stress, and cell death. Meanwhile, the immune microenvironment in GBM is...

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Main Authors: Rongze Olivia Lu, Winson S. Ho
Format: Article
Language:English
Published: Frontiers Media S.A. 2021-01-01
Series:Frontiers in Cell and Developmental Biology
Subjects:
Online Access:https://www.frontiersin.org/articles/10.3389/fcell.2020.620788/full
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spelling doaj-3c347484997a4bceb9dd4e242ba8c6b42021-01-15T05:13:11ZengFrontiers Media S.A.Frontiers in Cell and Developmental Biology2296-634X2021-01-01810.3389/fcell.2020.620788620788Mitochondrial Dysfunction, Macrophage, and Microglia in Brain CancerRongze Olivia Lu0Rongze Olivia Lu1Winson S. Ho2Winson S. Ho3Department of Neurosurgery, Dell Medical School, University of Texas at Austin, Austin, TX, United StatesMulva Clinic for the Neurosciences, Dell Medical School, University of Texas at Austin, Austin, TX, United StatesDepartment of Neurosurgery, Dell Medical School, University of Texas at Austin, Austin, TX, United StatesMulva Clinic for the Neurosciences, Dell Medical School, University of Texas at Austin, Austin, TX, United StatesGlioblastoma (GBM) is the most common malignant brain cancer. Increasing evidence suggests that mitochondrial dysfunction plays a key role in GBM progression as mitochondria is essential in regulating cell metabolism, oxidative stress, and cell death. Meanwhile, the immune microenvironment in GBM is predominated by tumor-associated macrophages and microglia (TAM), which is a heterogenous population of myeloid cells that, in general, create an immunosuppressive milieu to support tumor growth. However, subsets of TAMs can be pro-inflammatory and thereby antitumor. Therapeutic strategies targeting TAMs are increasingly explored as novel treatment strategies for GBM. The connection between mitochondrial dysfunction and TAMs phenotype in the tumor microenvironment is unclear. This review aims to provide perspectives and discuss possible molecular mechanisms mediating the interplay between glioma mitochondrial dysfunction and TAMs phenotype in shaping tumor immune microenvironment.https://www.frontiersin.org/articles/10.3389/fcell.2020.620788/fulltumor associated macrophages and microgliamitochondrial dysfunctionmitochondrial DNAbrain cancerinflammatory response
collection DOAJ
language English
format Article
sources DOAJ
author Rongze Olivia Lu
Rongze Olivia Lu
Winson S. Ho
Winson S. Ho
spellingShingle Rongze Olivia Lu
Rongze Olivia Lu
Winson S. Ho
Winson S. Ho
Mitochondrial Dysfunction, Macrophage, and Microglia in Brain Cancer
Frontiers in Cell and Developmental Biology
tumor associated macrophages and microglia
mitochondrial dysfunction
mitochondrial DNA
brain cancer
inflammatory response
author_facet Rongze Olivia Lu
Rongze Olivia Lu
Winson S. Ho
Winson S. Ho
author_sort Rongze Olivia Lu
title Mitochondrial Dysfunction, Macrophage, and Microglia in Brain Cancer
title_short Mitochondrial Dysfunction, Macrophage, and Microglia in Brain Cancer
title_full Mitochondrial Dysfunction, Macrophage, and Microglia in Brain Cancer
title_fullStr Mitochondrial Dysfunction, Macrophage, and Microglia in Brain Cancer
title_full_unstemmed Mitochondrial Dysfunction, Macrophage, and Microglia in Brain Cancer
title_sort mitochondrial dysfunction, macrophage, and microglia in brain cancer
publisher Frontiers Media S.A.
series Frontiers in Cell and Developmental Biology
issn 2296-634X
publishDate 2021-01-01
description Glioblastoma (GBM) is the most common malignant brain cancer. Increasing evidence suggests that mitochondrial dysfunction plays a key role in GBM progression as mitochondria is essential in regulating cell metabolism, oxidative stress, and cell death. Meanwhile, the immune microenvironment in GBM is predominated by tumor-associated macrophages and microglia (TAM), which is a heterogenous population of myeloid cells that, in general, create an immunosuppressive milieu to support tumor growth. However, subsets of TAMs can be pro-inflammatory and thereby antitumor. Therapeutic strategies targeting TAMs are increasingly explored as novel treatment strategies for GBM. The connection between mitochondrial dysfunction and TAMs phenotype in the tumor microenvironment is unclear. This review aims to provide perspectives and discuss possible molecular mechanisms mediating the interplay between glioma mitochondrial dysfunction and TAMs phenotype in shaping tumor immune microenvironment.
topic tumor associated macrophages and microglia
mitochondrial dysfunction
mitochondrial DNA
brain cancer
inflammatory response
url https://www.frontiersin.org/articles/10.3389/fcell.2020.620788/full
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