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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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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