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Canine tumor mutational burden is correlated with TP53 mutation across tumor types and breeds
Spontaneous canine cancers are valuable but relatively understudied and underutilized models. To enhance their usage, we reanalyze whole exome and genome sequencing data published for 684 cases of >7 common tumor types and >35 breeds, with rigorous quality control and breed validation. Our res...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8333103/ https://www.ncbi.nlm.nih.gov/pubmed/34344882 http://dx.doi.org/10.1038/s41467-021-24836-9 |
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author | Alsaihati, Burair A. Ho, Kun-Lin Watson, Joshua Feng, Yuan Wang, Tianfang Dobbin, Kevin K. Zhao, Shaying |
author_facet | Alsaihati, Burair A. Ho, Kun-Lin Watson, Joshua Feng, Yuan Wang, Tianfang Dobbin, Kevin K. Zhao, Shaying |
author_sort | Alsaihati, Burair A. |
collection | PubMed |
description | Spontaneous canine cancers are valuable but relatively understudied and underutilized models. To enhance their usage, we reanalyze whole exome and genome sequencing data published for 684 cases of >7 common tumor types and >35 breeds, with rigorous quality control and breed validation. Our results indicate that canine tumor alteration landscape is tumor type-dependent, but likely breed-independent. Each tumor type harbors major pathway alterations also found in its human counterpart (e.g., PI3K in mammary tumor and p53 in osteosarcoma). Mammary tumor and glioma have lower tumor mutational burden (TMB) (median < 0.5 mutations per Mb), whereas oral melanoma, osteosarcoma and hemangiosarcoma have higher TMB (median ≥ 1 mutations per Mb). Across tumor types and breeds, TMB is associated with mutation of TP53 but not PIK3CA, the most mutated genes. Golden Retrievers harbor a TMB-associated and osteosarcoma-enriched mutation signature. Here, we provide a snapshot of canine mutations across major tumor types and breeds. |
format | Online Article Text |
id | pubmed-8333103 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-83331032021-08-12 Canine tumor mutational burden is correlated with TP53 mutation across tumor types and breeds Alsaihati, Burair A. Ho, Kun-Lin Watson, Joshua Feng, Yuan Wang, Tianfang Dobbin, Kevin K. Zhao, Shaying Nat Commun Article Spontaneous canine cancers are valuable but relatively understudied and underutilized models. To enhance their usage, we reanalyze whole exome and genome sequencing data published for 684 cases of >7 common tumor types and >35 breeds, with rigorous quality control and breed validation. Our results indicate that canine tumor alteration landscape is tumor type-dependent, but likely breed-independent. Each tumor type harbors major pathway alterations also found in its human counterpart (e.g., PI3K in mammary tumor and p53 in osteosarcoma). Mammary tumor and glioma have lower tumor mutational burden (TMB) (median < 0.5 mutations per Mb), whereas oral melanoma, osteosarcoma and hemangiosarcoma have higher TMB (median ≥ 1 mutations per Mb). Across tumor types and breeds, TMB is associated with mutation of TP53 but not PIK3CA, the most mutated genes. Golden Retrievers harbor a TMB-associated and osteosarcoma-enriched mutation signature. Here, we provide a snapshot of canine mutations across major tumor types and breeds. Nature Publishing Group UK 2021-08-03 /pmc/articles/PMC8333103/ /pubmed/34344882 http://dx.doi.org/10.1038/s41467-021-24836-9 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Alsaihati, Burair A. Ho, Kun-Lin Watson, Joshua Feng, Yuan Wang, Tianfang Dobbin, Kevin K. Zhao, Shaying Canine tumor mutational burden is correlated with TP53 mutation across tumor types and breeds |
title | Canine tumor mutational burden is correlated with TP53 mutation across tumor types and breeds |
title_full | Canine tumor mutational burden is correlated with TP53 mutation across tumor types and breeds |
title_fullStr | Canine tumor mutational burden is correlated with TP53 mutation across tumor types and breeds |
title_full_unstemmed | Canine tumor mutational burden is correlated with TP53 mutation across tumor types and breeds |
title_short | Canine tumor mutational burden is correlated with TP53 mutation across tumor types and breeds |
title_sort | canine tumor mutational burden is correlated with tp53 mutation across tumor types and breeds |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8333103/ https://www.ncbi.nlm.nih.gov/pubmed/34344882 http://dx.doi.org/10.1038/s41467-021-24836-9 |
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