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Identification of additional mitochondrial DNA mutations in canine mast cell tumours
BACKGROUND: Research has revealed the presence of somatic mutations in mitochondrial DNA (mtDNA) of certain types of tumours. As this has not been studied for canine mast cell tumours, the aim of this study was to identify mutations in the hypervariable region of mtDNA in mast cell tumours in dogs a...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4855722/ https://www.ncbi.nlm.nih.gov/pubmed/27146669 http://dx.doi.org/10.1186/s13028-016-0210-y |
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author | Śmiech, Anna Ślaska, Brygida Surdyka, Magdalena Grzybowska-Szatkowska, Ludmiła Łopuszyński, Wojciech Różańska, Dorota |
author_facet | Śmiech, Anna Ślaska, Brygida Surdyka, Magdalena Grzybowska-Szatkowska, Ludmiła Łopuszyński, Wojciech Różańska, Dorota |
author_sort | Śmiech, Anna |
collection | PubMed |
description | BACKGROUND: Research has revealed the presence of somatic mutations in mitochondrial DNA (mtDNA) of certain types of tumours. As this has not been studied for canine mast cell tumours, the aim of this study was to identify mutations in the hypervariable region of mtDNA in mast cell tumours in dogs and determine their association with the process of neoplastic transformation. RESULTS: Samples from 17 dogs with histopathologically confirmed mast cell tumours were analysed. The samples consisted of tumour tissues (n = 17), normal tissues (n = 17), and blood (n = 17). Amplicons of the displacement loop (D-loop) were sequenced and the obtained nucleotide sequences were subjected to bioinformatics analyses. Somatic mutations were detected in seven positions of the D-loop nucleotide sequences in 47 % of the dogs, while polymorphisms were identified in 94 % of the dogs. Most of these changes were homoplasmic, while heteroplasmy was detected in two individuals. Six new haplotypes were established as being characteristic for canine mast cell tumours. There was no association between the presence of the mutations and sex, haplotype, or malignancy grade assessed in 3 and 2-grade scales. CONCLUSIONS: Differences in the frequency of somatic mutations imply their direct association with the neoplastic transformation. However, their functional consequences and clinical significance are not clear. The mutations may be used for diagnosis and prognosis of canine mast cell tumours in the future. |
format | Online Article Text |
id | pubmed-4855722 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-48557222016-05-05 Identification of additional mitochondrial DNA mutations in canine mast cell tumours Śmiech, Anna Ślaska, Brygida Surdyka, Magdalena Grzybowska-Szatkowska, Ludmiła Łopuszyński, Wojciech Różańska, Dorota Acta Vet Scand Brief Communication BACKGROUND: Research has revealed the presence of somatic mutations in mitochondrial DNA (mtDNA) of certain types of tumours. As this has not been studied for canine mast cell tumours, the aim of this study was to identify mutations in the hypervariable region of mtDNA in mast cell tumours in dogs and determine their association with the process of neoplastic transformation. RESULTS: Samples from 17 dogs with histopathologically confirmed mast cell tumours were analysed. The samples consisted of tumour tissues (n = 17), normal tissues (n = 17), and blood (n = 17). Amplicons of the displacement loop (D-loop) were sequenced and the obtained nucleotide sequences were subjected to bioinformatics analyses. Somatic mutations were detected in seven positions of the D-loop nucleotide sequences in 47 % of the dogs, while polymorphisms were identified in 94 % of the dogs. Most of these changes were homoplasmic, while heteroplasmy was detected in two individuals. Six new haplotypes were established as being characteristic for canine mast cell tumours. There was no association between the presence of the mutations and sex, haplotype, or malignancy grade assessed in 3 and 2-grade scales. CONCLUSIONS: Differences in the frequency of somatic mutations imply their direct association with the neoplastic transformation. However, their functional consequences and clinical significance are not clear. The mutations may be used for diagnosis and prognosis of canine mast cell tumours in the future. BioMed Central 2016-05-04 /pmc/articles/PMC4855722/ /pubmed/27146669 http://dx.doi.org/10.1186/s13028-016-0210-y Text en © Śmiech et al. 2016 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 | Brief Communication Śmiech, Anna Ślaska, Brygida Surdyka, Magdalena Grzybowska-Szatkowska, Ludmiła Łopuszyński, Wojciech Różańska, Dorota Identification of additional mitochondrial DNA mutations in canine mast cell tumours |
title | Identification of additional mitochondrial DNA mutations in canine mast cell tumours |
title_full | Identification of additional mitochondrial DNA mutations in canine mast cell tumours |
title_fullStr | Identification of additional mitochondrial DNA mutations in canine mast cell tumours |
title_full_unstemmed | Identification of additional mitochondrial DNA mutations in canine mast cell tumours |
title_short | Identification of additional mitochondrial DNA mutations in canine mast cell tumours |
title_sort | identification of additional mitochondrial dna mutations in canine mast cell tumours |
topic | Brief Communication |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4855722/ https://www.ncbi.nlm.nih.gov/pubmed/27146669 http://dx.doi.org/10.1186/s13028-016-0210-y |
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