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Transgenic Res. 2017 Oct;26(5):603-612. doi: 10.1007/s11248-017-0031-4. Epub 2017 Jun 29.

Pancreas specific expression of oncogenes in a porcine model.

Author information

1
Department of Clinical Medicine, Aarhus University, 8200, Aarhus N, Denmark.
2
Department of Biomedicine, Aarhus University, 8000, Aarhus C, Denmark.
3
Department of Animal Science, Aarhus University, 8830, Tjele, Denmark.
4
Institute of Pathology, Aarhus University Hospital, 8000, Aarhus C, Denmark.
5
Department of Clinical Medicine, Aarhus University, 8200, Aarhus N, Denmark. mkt@clin.au.dk.
6
Department of Biomedicine, Aarhus University, 8000, Aarhus C, Denmark. mkt@clin.au.dk.

Abstract

Pancreatic cancer is the fourth leading course of cancer death and early detection of the disease is crucial for successful treatment. However, pancreatic cancer is difficult to detect in its earliest stages and once symptoms appear, the cancer has often progressed beyond possibility for curing. Research into the disease has been hampered by the lack of good models. We have generated a porcine model of pancreatic cancer with use of transgenic overexpression of an oncogene cassette containing MYC, KRAS G12D and SV40 LT. The expression was initiated from a modified Pdx-1 promoter during embryogenesis in a subset of pancreatic epithelial cells. Furthermore, cells expressing the oncogenes also expressed a yellow fluorescent protein (mVenus) and an inducible negative regulator protein (rtTR-KRAB). Cells where the Pdx-1 promoter had not been activated, expressed a red fluorescent protein (Katushka). In vitro analyses of cells obtained from the transgenic pigs showed increased proliferation and expression of the transgenes when activated. Induction of the repressor protein eliminated the oncogene expression and decreased cell proliferation. In vivo analysis identified foci of pancreatic cells expressing the oncogenes at day zero post farrowing. These populations expanded and formed hyperplastic foci, with beginning abnormality at day 45. Cells in the foci expressed the oncogenic proteins and the majority of the cells were positive for the proliferation marker, Ki67. We predict that this model could be used for advanced studies in pancreatic cancer in a large animal model with focus on early detection, treatment, and identification of new biomarkers.

KEYWORDS:

Gene activation and repression; Oncogenes; Pancreatic cancer; Pig model; Somatic cell nuclear transfer

PMID:
28664456
DOI:
10.1007/s11248-017-0031-4
[Indexed for MEDLINE]

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