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Targeted oncogenesis of hormone-negative pancreatic islet progenitor cells

By Thomas L. Jetton, J. Michael Moates, Jill Lindner, Christopher V. E. Wright and Mark A. Magnuson

Abstract

Transgenic mice containing an upstream glucokinase (βGK) promoter– simian virus 40 T antigen (Tag) fusion gene develop neuroendocrine tumors primarily in the pancreas, gut, and pituitary. Pancreatic tumors from a line with delayed tumorigenesis were of two different types: insulinomas and noninsulinomas. The noninsulinomas are often periductal in location, express none of the four major islet peptide hormones, Glut-2, Pdx1, tyrosine hydroxylase, Pax4, Pax6, or Nkx6.1, but do express glucokinase, Sur1, Isl1, Hnf3β, Hnf6, Beta2/NeuroD, and Nkx2.2. Cells from two different noninsulinoma tumors, when adapted to culture, began to express either insulin, glucagon, or somatostatin. Given the partial gene expression repertoire of the noninsulinoma tumors, their apparent periductal origin, and the ability of these cells to partially cytodifferentiate in culture, we suggest that these tumors are derived from islet progenitor cells. Thus, βGK–Tag transgenic mice provide a new model system for studying the events that occur during both islet cell neogenesis and normal embryonic development

Topics: Biological Sciences
Publisher: The National Academy of Sciences
Year: 1998
DOI identifier: 10.1073/pnas.95.15.8654
OAI identifier: oai:pubmedcentral.nih.gov:21131
Provided by: PubMed Central
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