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A Genetic Porcine Model of Cancer
Author(s) -
Lawrence B. Schook,
Tiago Collares,
Wenping Hu,
Ying Liang,
Fernanda Martins Rodrigues,
Laurie A. Rund,
Kyle M. Schachtschneider,
Fabiana K. Seixas,
Kuldeep Singh,
Kevin D. Wells,
Eric M. Walters,
Randall S. Prather,
Christopher M. Counter
Publication year - 2015
Publication title -
plos one
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.99
H-Index - 332
ISSN - 1932-6203
DOI - 10.1371/journal.pone.0128864
Subject(s) - biology , transgene , cre recombinase , oncogene , genetically modified mouse , cancer , cancer research , carcinogenesis , genetically modified organism , green fluorescent protein , microbiology and biotechnology , gene , computational biology , genetics , cell cycle
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.

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