Abstract
We created gene-targeted pigs with mutations in the adenomatous polyposis coli (APC) gene (APC) that are orthologous to those responsible for human familial adenomatous polyposis (FAP). One-year-old pigs with the APC 1311 mutation (orthologous to human APC1309) have aberrant crypt foci and low- and high-grade dysplastic adenomas in the large intestine, similar to the precancerous lesions that develop in patients with FAP. Dysplastic adenomas accumulate β-catenin and lose heterozygosity of APC. This large-animal, genetic model of FAP will be useful in the development of diagnostics and therapeutics for colorectal cancer. DNA sequence data: NCBI accession number GU951771. © 2012 AGA Institute.
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Flisikowska, T., Merkl, C., Landmann, M., Eser, S., Rezaei, N., Cui, X., … Schnieke, A. (2012). A porcine model of familial adenomatous polyposis. Gastroenterology, 143(5). https://doi.org/10.1053/j.gastro.2012.07.110
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