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Preinvasive and invasive ductal pancreatic cancer and its early detection in the mouse.

Cancer cell | Dec 6, 2003

http://www.ncbi.nlm.nih.gov/pubmed/14706336

To evaluate the role of oncogenic RAS mutations in pancreatic tumorigenesis, we directed endogenous expression of KRAS(G12D) to progenitor cells of the mouse pancreas. We find that physiological levels of Kras(G12D) induce ductal lesions that recapitulate the full spectrum of human pancreatic intraepithelial neoplasias (PanINs), putative precursors to invasive pancreatic cancer. The PanINs are highly proliferative, show evidence of histological progression, and activate signaling pathways normally quiescent in ductal epithelium, suggesting potential therapeutic and chemopreventive targets for the cognate human condition. At low frequency, these lesions also progress spontaneously to invasive and metastatic adenocarcinomas, establishing PanINs as definitive precursors to the invasive disease. Finally, mice with PanINs have an identifiable serum proteomic signature, suggesting a means of detecting the preinvasive state in patients.

Pubmed ID: 14706336 RIS Download

Mesh terms: Animals | Basic Helix-Loop-Helix Transcription Factors | Carcinoma, Pancreatic Ductal | Cyclooxygenase 2 | Genes, ras | Homeodomain Proteins | Humans | Immunohistochemistry | Isoenzymes | Matrix Metalloproteinase 7 | Membrane Proteins | Mice | Mutation | Neoplasm Metastasis | Neoplasm Staging | Pancreas | Pancreatic Neoplasms | Prostaglandin-Endoperoxide Synthases

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Associated grants

  • Agency: NIDDK NIH HHS, Id: P30 DK050306
  • Agency: NCI NIH HHS, Id: P50-CA-62924
  • Agency: NCI NIH HHS, Id: R25-CA87812

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