4.6 Article

A Genetic Porcine Model of Cancer

Journal

PLOS ONE
Volume 10, Issue 7, Pages -

Publisher

PUBLIC LIBRARY SCIENCE
DOI: 10.1371/journal.pone.0128864

Keywords

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Funding

  1. China Scholarship Council (CSC)
  2. Brazilian Scholarship Program Science Without Borders promoted by the National Counsel of Technological and Scientific Development
  3. American Cancer Society [ACS178898]
  4. U.S. National Institutes of Health [CA123031, CA 153132, U42 OD011140]
  5. Edward Spiegel Fund of the Lymphoma Foundation
  6. United States Department of Agriculture (USDA) [AG 58-5438-2-307]
  7. Edward William & Jane Marr Gutgsell Foundation
  8. Cooperative Research Program for Agriculture Science & Technology Development [PJ009103]
  9. Rural Development Administration, Republic of Korea

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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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