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Mitochondria in tumour progression: a network of mtDNA variants in different types of cancer
BACKGROUND: Mitochondrial participation in tumorigenesis and metastasis has been studied for many years, but several aspects of this mechanism remain unclear, such as the association of mitochondrial DNA (mtDNA) with different cancers. Here, based on two independent datasets, we modelled an mtDNA mu...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8857862/ https://www.ncbi.nlm.nih.gov/pubmed/35183124 http://dx.doi.org/10.1186/s12863-022-01032-2 |
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author | Cavalcante, Giovanna C. Ribeiro-dos-Santos, Ândrea de Araújo, Gilderlanio S. |
author_facet | Cavalcante, Giovanna C. Ribeiro-dos-Santos, Ândrea de Araújo, Gilderlanio S. |
author_sort | Cavalcante, Giovanna C. |
collection | PubMed |
description | BACKGROUND: Mitochondrial participation in tumorigenesis and metastasis has been studied for many years, but several aspects of this mechanism remain unclear, such as the association of mitochondrial DNA (mtDNA) with different cancers. Here, based on two independent datasets, we modelled an mtDNA mutation-cancer network by systematic integrative analysis including 37 cancer types to identify the mitochondrial variants found in common among them. RESULTS: Our network showed mtDNA associations between gastric cancer and other cancer types, particularly kidney, liver, and prostate cancers, which is suggestive of a potential role of such variants in the metastatic processes among these cancer types. A graph-based interactive web tool was made available at www2.lghm.ufpa.br/mtdna. We also highlighted that most shared variants were in the MT-ND4, MT-ND5 and D-loop, and that some of these variants were nonsynonymous, indicating a special importance of these variants and regions regarding cancer progression, involving genomic and epigenomic alterations. CONCLUSIONS: This study reinforces the importance of studying mtDNA in cancer and offers new perspectives on the potential involvement of different mitochondrial variants in cancer development and metastasis. |
format | Online Article Text |
id | pubmed-8857862 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-88578622022-02-23 Mitochondria in tumour progression: a network of mtDNA variants in different types of cancer Cavalcante, Giovanna C. Ribeiro-dos-Santos, Ândrea de Araújo, Gilderlanio S. BMC Genom Data Research BACKGROUND: Mitochondrial participation in tumorigenesis and metastasis has been studied for many years, but several aspects of this mechanism remain unclear, such as the association of mitochondrial DNA (mtDNA) with different cancers. Here, based on two independent datasets, we modelled an mtDNA mutation-cancer network by systematic integrative analysis including 37 cancer types to identify the mitochondrial variants found in common among them. RESULTS: Our network showed mtDNA associations between gastric cancer and other cancer types, particularly kidney, liver, and prostate cancers, which is suggestive of a potential role of such variants in the metastatic processes among these cancer types. A graph-based interactive web tool was made available at www2.lghm.ufpa.br/mtdna. We also highlighted that most shared variants were in the MT-ND4, MT-ND5 and D-loop, and that some of these variants were nonsynonymous, indicating a special importance of these variants and regions regarding cancer progression, involving genomic and epigenomic alterations. CONCLUSIONS: This study reinforces the importance of studying mtDNA in cancer and offers new perspectives on the potential involvement of different mitochondrial variants in cancer development and metastasis. BioMed Central 2022-02-18 /pmc/articles/PMC8857862/ /pubmed/35183124 http://dx.doi.org/10.1186/s12863-022-01032-2 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Cavalcante, Giovanna C. Ribeiro-dos-Santos, Ândrea de Araújo, Gilderlanio S. Mitochondria in tumour progression: a network of mtDNA variants in different types of cancer |
title | Mitochondria in tumour progression: a network of mtDNA variants in different types of cancer |
title_full | Mitochondria in tumour progression: a network of mtDNA variants in different types of cancer |
title_fullStr | Mitochondria in tumour progression: a network of mtDNA variants in different types of cancer |
title_full_unstemmed | Mitochondria in tumour progression: a network of mtDNA variants in different types of cancer |
title_short | Mitochondria in tumour progression: a network of mtDNA variants in different types of cancer |
title_sort | mitochondria in tumour progression: a network of mtdna variants in different types of cancer |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8857862/ https://www.ncbi.nlm.nih.gov/pubmed/35183124 http://dx.doi.org/10.1186/s12863-022-01032-2 |
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