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Characterization of the Human Papillomavirus 16 Oncogenes in K14HPV16 Mice: Sublineage A1 Drives Multi-Organ Carcinogenesis
The study of human papillomavirus (HPV)-induced carcinogenesis uses multiple in vivo mouse models, one of which relies on the cytokeratin 14 gene promoter to drive the expression of all HPV early oncogenes. This study aimed to determine the HPV16 variant and sublineage present in the K14HPV16 mouse...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9604181/ https://www.ncbi.nlm.nih.gov/pubmed/36293226 http://dx.doi.org/10.3390/ijms232012371 |
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author | Cochicho, Daniela Nunes, Alexandra Gomes, João Paulo Martins, Luís Cunha, Mário Medeiros-Fonseca, Beatriz Oliveira, Paula Bastos, Margarida M. S. M. Medeiros, Rui Mendonça, Joana Vieira, Luis Gil da Costa, Rui M. Felix, Ana |
author_facet | Cochicho, Daniela Nunes, Alexandra Gomes, João Paulo Martins, Luís Cunha, Mário Medeiros-Fonseca, Beatriz Oliveira, Paula Bastos, Margarida M. S. M. Medeiros, Rui Mendonça, Joana Vieira, Luis Gil da Costa, Rui M. Felix, Ana |
author_sort | Cochicho, Daniela |
collection | PubMed |
description | The study of human papillomavirus (HPV)-induced carcinogenesis uses multiple in vivo mouse models, one of which relies on the cytokeratin 14 gene promoter to drive the expression of all HPV early oncogenes. This study aimed to determine the HPV16 variant and sublineage present in the K14HPV16 mouse model. This information can be considered of great importance to further enhance this K14HPV16 model as an essential research tool and optimize its use for basic and translational studies. Our study evaluated HPV DNA from 17 samples isolated from 4 animals, both wild-type (n = 2) and HPV16-transgenic mice (n = 2). Total DNA was extracted from tissues and the detection of HPV16 was performed using a qPCR multiplex. HPV16-positive samples were subsequently whole-genome sequenced by next-generation sequencing techniques. The phylogenetic positioning clearly shows K14HPV16 samples clustering together in the sub-lineage A1 (NC001526.4). A comparative genome analysis of K14HPV16 samples revealed three mutations to the human papillomaviruses type 16 sublineage A1 representative strain. Knowledge of the HPV 16 variant is fundamental, and these findings will allow the rational use of this animal model to explore the role of the A1 sublineage in HPV-driven cancer. |
format | Online Article Text |
id | pubmed-9604181 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-96041812022-10-27 Characterization of the Human Papillomavirus 16 Oncogenes in K14HPV16 Mice: Sublineage A1 Drives Multi-Organ Carcinogenesis Cochicho, Daniela Nunes, Alexandra Gomes, João Paulo Martins, Luís Cunha, Mário Medeiros-Fonseca, Beatriz Oliveira, Paula Bastos, Margarida M. S. M. Medeiros, Rui Mendonça, Joana Vieira, Luis Gil da Costa, Rui M. Felix, Ana Int J Mol Sci Article The study of human papillomavirus (HPV)-induced carcinogenesis uses multiple in vivo mouse models, one of which relies on the cytokeratin 14 gene promoter to drive the expression of all HPV early oncogenes. This study aimed to determine the HPV16 variant and sublineage present in the K14HPV16 mouse model. This information can be considered of great importance to further enhance this K14HPV16 model as an essential research tool and optimize its use for basic and translational studies. Our study evaluated HPV DNA from 17 samples isolated from 4 animals, both wild-type (n = 2) and HPV16-transgenic mice (n = 2). Total DNA was extracted from tissues and the detection of HPV16 was performed using a qPCR multiplex. HPV16-positive samples were subsequently whole-genome sequenced by next-generation sequencing techniques. The phylogenetic positioning clearly shows K14HPV16 samples clustering together in the sub-lineage A1 (NC001526.4). A comparative genome analysis of K14HPV16 samples revealed three mutations to the human papillomaviruses type 16 sublineage A1 representative strain. Knowledge of the HPV 16 variant is fundamental, and these findings will allow the rational use of this animal model to explore the role of the A1 sublineage in HPV-driven cancer. MDPI 2022-10-15 /pmc/articles/PMC9604181/ /pubmed/36293226 http://dx.doi.org/10.3390/ijms232012371 Text en © 2022 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 | Article Cochicho, Daniela Nunes, Alexandra Gomes, João Paulo Martins, Luís Cunha, Mário Medeiros-Fonseca, Beatriz Oliveira, Paula Bastos, Margarida M. S. M. Medeiros, Rui Mendonça, Joana Vieira, Luis Gil da Costa, Rui M. Felix, Ana Characterization of the Human Papillomavirus 16 Oncogenes in K14HPV16 Mice: Sublineage A1 Drives Multi-Organ Carcinogenesis |
title | Characterization of the Human Papillomavirus 16 Oncogenes in K14HPV16 Mice: Sublineage A1 Drives Multi-Organ Carcinogenesis |
title_full | Characterization of the Human Papillomavirus 16 Oncogenes in K14HPV16 Mice: Sublineage A1 Drives Multi-Organ Carcinogenesis |
title_fullStr | Characterization of the Human Papillomavirus 16 Oncogenes in K14HPV16 Mice: Sublineage A1 Drives Multi-Organ Carcinogenesis |
title_full_unstemmed | Characterization of the Human Papillomavirus 16 Oncogenes in K14HPV16 Mice: Sublineage A1 Drives Multi-Organ Carcinogenesis |
title_short | Characterization of the Human Papillomavirus 16 Oncogenes in K14HPV16 Mice: Sublineage A1 Drives Multi-Organ Carcinogenesis |
title_sort | characterization of the human papillomavirus 16 oncogenes in k14hpv16 mice: sublineage a1 drives multi-organ carcinogenesis |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9604181/ https://www.ncbi.nlm.nih.gov/pubmed/36293226 http://dx.doi.org/10.3390/ijms232012371 |
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