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Mitochondrial DNA: the overlooked oncogenome?

Perturbed mitochondrial bioenergetics constitute a core pillar of cancer-associated metabolic dysfunction. While mitochondrial dysfunction in cancer may result from myriad biochemical causes, a historically neglected source is that of the mitochondrial genome. Recent large-scale sequencing efforts a...

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Detalles Bibliográficos
Autores principales: Gammage, Payam A., Frezza, Christian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6615100/
https://www.ncbi.nlm.nih.gov/pubmed/31286943
http://dx.doi.org/10.1186/s12915-019-0668-y
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author Gammage, Payam A.
Frezza, Christian
author_facet Gammage, Payam A.
Frezza, Christian
author_sort Gammage, Payam A.
collection PubMed
description Perturbed mitochondrial bioenergetics constitute a core pillar of cancer-associated metabolic dysfunction. While mitochondrial dysfunction in cancer may result from myriad biochemical causes, a historically neglected source is that of the mitochondrial genome. Recent large-scale sequencing efforts and clinical studies have highlighted the prevalence of mutations in mitochondrial DNA (mtDNA) in human tumours and their potential roles in cancer progression. In this review we discuss the biology of the mitochondrial genome, sources of mtDNA mutations, and experimental evidence of a role for mtDNA mutations in cancer. We also propose a ‘metabolic licensing’ model for mtDNA mutation-derived dysfunction in cancer initiation and progression.
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spelling pubmed-66151002019-07-18 Mitochondrial DNA: the overlooked oncogenome? Gammage, Payam A. Frezza, Christian BMC Biol Review Perturbed mitochondrial bioenergetics constitute a core pillar of cancer-associated metabolic dysfunction. While mitochondrial dysfunction in cancer may result from myriad biochemical causes, a historically neglected source is that of the mitochondrial genome. Recent large-scale sequencing efforts and clinical studies have highlighted the prevalence of mutations in mitochondrial DNA (mtDNA) in human tumours and their potential roles in cancer progression. In this review we discuss the biology of the mitochondrial genome, sources of mtDNA mutations, and experimental evidence of a role for mtDNA mutations in cancer. We also propose a ‘metabolic licensing’ model for mtDNA mutation-derived dysfunction in cancer initiation and progression. BioMed Central 2019-07-08 /pmc/articles/PMC6615100/ /pubmed/31286943 http://dx.doi.org/10.1186/s12915-019-0668-y Text en © The Author(s). 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Review
Gammage, Payam A.
Frezza, Christian
Mitochondrial DNA: the overlooked oncogenome?
title Mitochondrial DNA: the overlooked oncogenome?
title_full Mitochondrial DNA: the overlooked oncogenome?
title_fullStr Mitochondrial DNA: the overlooked oncogenome?
title_full_unstemmed Mitochondrial DNA: the overlooked oncogenome?
title_short Mitochondrial DNA: the overlooked oncogenome?
title_sort mitochondrial dna: the overlooked oncogenome?
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6615100/
https://www.ncbi.nlm.nih.gov/pubmed/31286943
http://dx.doi.org/10.1186/s12915-019-0668-y
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