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Mitochondrial DNA Alterations in Glioblastoma (GBM)

Glioblastoma (GBM) is an extremely aggressive tumor originating from neural stem cells of the central nervous system, which has high histopathological and genomic diversity. Mitochondria are cellular organelles associated with the regulation of cellular metabolism, redox signaling, energy generation...

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Detalles Bibliográficos
Autores principales: Leão Barros, Mariceli Baia, Pinheiro, Danilo do Rosário, Borges, Bárbara do Nascimento
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8199454/
https://www.ncbi.nlm.nih.gov/pubmed/34072607
http://dx.doi.org/10.3390/ijms22115855
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author Leão Barros, Mariceli Baia
Pinheiro, Danilo do Rosário
Borges, Bárbara do Nascimento
author_facet Leão Barros, Mariceli Baia
Pinheiro, Danilo do Rosário
Borges, Bárbara do Nascimento
author_sort Leão Barros, Mariceli Baia
collection PubMed
description Glioblastoma (GBM) is an extremely aggressive tumor originating from neural stem cells of the central nervous system, which has high histopathological and genomic diversity. Mitochondria are cellular organelles associated with the regulation of cellular metabolism, redox signaling, energy generation, regulation of cell proliferation, and apoptosis. Accumulation of mutations in mitochondrial DNA (mtDNA) leads to mitochondrial dysfunction that plays an important role in GBM pathogenesis, favoring abnormal energy and reactive oxygen species production and resistance to apoptosis and to chemotherapeutic agents. The present review summarizes the known mitochondrial DNA alterations related to GBM, their cellular and metabolic consequences, and their association with diagnosis, prognosis, and treatment.
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spelling pubmed-81994542021-06-14 Mitochondrial DNA Alterations in Glioblastoma (GBM) Leão Barros, Mariceli Baia Pinheiro, Danilo do Rosário Borges, Bárbara do Nascimento Int J Mol Sci Review Glioblastoma (GBM) is an extremely aggressive tumor originating from neural stem cells of the central nervous system, which has high histopathological and genomic diversity. Mitochondria are cellular organelles associated with the regulation of cellular metabolism, redox signaling, energy generation, regulation of cell proliferation, and apoptosis. Accumulation of mutations in mitochondrial DNA (mtDNA) leads to mitochondrial dysfunction that plays an important role in GBM pathogenesis, favoring abnormal energy and reactive oxygen species production and resistance to apoptosis and to chemotherapeutic agents. The present review summarizes the known mitochondrial DNA alterations related to GBM, their cellular and metabolic consequences, and their association with diagnosis, prognosis, and treatment. MDPI 2021-05-29 /pmc/articles/PMC8199454/ /pubmed/34072607 http://dx.doi.org/10.3390/ijms22115855 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Leão Barros, Mariceli Baia
Pinheiro, Danilo do Rosário
Borges, Bárbara do Nascimento
Mitochondrial DNA Alterations in Glioblastoma (GBM)
title Mitochondrial DNA Alterations in Glioblastoma (GBM)
title_full Mitochondrial DNA Alterations in Glioblastoma (GBM)
title_fullStr Mitochondrial DNA Alterations in Glioblastoma (GBM)
title_full_unstemmed Mitochondrial DNA Alterations in Glioblastoma (GBM)
title_short Mitochondrial DNA Alterations in Glioblastoma (GBM)
title_sort mitochondrial dna alterations in glioblastoma (gbm)
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8199454/
https://www.ncbi.nlm.nih.gov/pubmed/34072607
http://dx.doi.org/10.3390/ijms22115855
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