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A Genetic Porcine Model of Cancer
The large size of the pig and its similarity in anatomy, physiology, metabolism, and genetics to humans make it an ideal platform to develop a genetically defined, large animal model of cancer. To this end, we created a transgenic “oncopig” line encoding Cre recombinase inducible porcine transgenes...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4488487/ https://www.ncbi.nlm.nih.gov/pubmed/26132737 http://dx.doi.org/10.1371/journal.pone.0128864 |
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author | Schook, Lawrence B. Collares, Tiago V. Hu, Wenping Liang, Ying Rodrigues, Fernanda M. Rund, Laurie A. Schachtschneider, Kyle M. Seixas, Fabiana K. Singh, Kuldeep Wells, Kevin D. Walters, Eric M. Prather, Randall S. Counter, Christopher M. |
author_facet | Schook, Lawrence B. Collares, Tiago V. Hu, Wenping Liang, Ying Rodrigues, Fernanda M. Rund, Laurie A. Schachtschneider, Kyle M. Seixas, Fabiana K. Singh, Kuldeep Wells, Kevin D. Walters, Eric M. Prather, Randall S. Counter, Christopher M. |
author_sort | Schook, Lawrence B. |
collection | PubMed |
description | The large size of the pig and its similarity in anatomy, physiology, metabolism, and genetics to humans make it an ideal platform to develop a genetically defined, large animal model of cancer. To this end, we created a transgenic “oncopig” line encoding Cre recombinase inducible porcine transgenes encoding KRAS(G12D) and TP53(R167H), which represent a commonly mutated oncogene and tumor suppressor in human cancers, respectively. Treatment of cells derived from these oncopigs with the adenovirus encoding Cre (AdCre) led to KRAS(G12D) and TP53(R167H) expression, which rendered the cells transformed in culture and tumorigenic when engrafted into immunocompromised mice. Finally, injection of AdCre directly into these oncopigs led to the rapid and reproducible tumor development of mesenchymal origin. Transgenic animals receiving AdGFP (green fluorescent protein) did not have any tumor mass formation or altered histopathology. This oncopig line could thus serve as a genetically malleable model for potentially a wide spectrum of cancers, while controlling for temporal or spatial genesis, which should prove invaluable to studies previously hampered by the lack of a large animal model of cancer. |
format | Online Article Text |
id | pubmed-4488487 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-44884872015-07-14 A Genetic Porcine Model of Cancer Schook, Lawrence B. Collares, Tiago V. Hu, Wenping Liang, Ying Rodrigues, Fernanda M. Rund, Laurie A. Schachtschneider, Kyle M. Seixas, Fabiana K. Singh, Kuldeep Wells, Kevin D. Walters, Eric M. Prather, Randall S. Counter, Christopher M. PLoS One Research Article The large size of the pig and its similarity in anatomy, physiology, metabolism, and genetics to humans make it an ideal platform to develop a genetically defined, large animal model of cancer. To this end, we created a transgenic “oncopig” line encoding Cre recombinase inducible porcine transgenes encoding KRAS(G12D) and TP53(R167H), which represent a commonly mutated oncogene and tumor suppressor in human cancers, respectively. Treatment of cells derived from these oncopigs with the adenovirus encoding Cre (AdCre) led to KRAS(G12D) and TP53(R167H) expression, which rendered the cells transformed in culture and tumorigenic when engrafted into immunocompromised mice. Finally, injection of AdCre directly into these oncopigs led to the rapid and reproducible tumor development of mesenchymal origin. Transgenic animals receiving AdGFP (green fluorescent protein) did not have any tumor mass formation or altered histopathology. This oncopig line could thus serve as a genetically malleable model for potentially a wide spectrum of cancers, while controlling for temporal or spatial genesis, which should prove invaluable to studies previously hampered by the lack of a large animal model of cancer. Public Library of Science 2015-07-01 /pmc/articles/PMC4488487/ /pubmed/26132737 http://dx.doi.org/10.1371/journal.pone.0128864 Text en © 2015 Schook et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Schook, Lawrence B. Collares, Tiago V. Hu, Wenping Liang, Ying Rodrigues, Fernanda M. Rund, Laurie A. Schachtschneider, Kyle M. Seixas, Fabiana K. Singh, Kuldeep Wells, Kevin D. Walters, Eric M. Prather, Randall S. Counter, Christopher M. A Genetic Porcine Model of Cancer |
title | A Genetic Porcine Model of Cancer |
title_full | A Genetic Porcine Model of Cancer |
title_fullStr | A Genetic Porcine Model of Cancer |
title_full_unstemmed | A Genetic Porcine Model of Cancer |
title_short | A Genetic Porcine Model of Cancer |
title_sort | genetic porcine model of cancer |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4488487/ https://www.ncbi.nlm.nih.gov/pubmed/26132737 http://dx.doi.org/10.1371/journal.pone.0128864 |
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