Abstract | OBJECTIVES: Earlier studies indicated that hamster pancreatic ductal adenocarcinoma not only derives from ductal/ductular structures but also from cells within the islet. So far unidentified cells within the islet are responsive to the carcinogenic effect of N-nitrosobis (2-oxopropyl) amine (BOP) forming poorly differentiated ductal adenocarcinoma. However, studies indicated a major role of β-cells during carcinogenesis. To find out, if β-cells are the primary target cells of BOP and if they are capable to form ductal adenocarcinoma after malignant transformation, we established a long-term culture of undifferentiated cells deriving from isolated β-cells and treated them with BOP. METHODS: Langerhans' islets from pancreata of Syrian golden hamsters were isolated and dispersed into single cells by dispase digestion. Cells were labeled with a highly specific β-cell surface antibody (K14D10) and these K14D10+ cells were extracted from the suspension by paramagnetic Dynabeads. Cells were cultured in vitro and treated with BOP. Untreated cells served as control. RESULTS: K14D10+ cells formed a monolayer and produced insulin over a period of 28 days in culture. However, with time in culture they became undifferentiated with a higher proliferation rate and after about 60 days in culture BOP treated cells showed anchorage independent growth. These cells autotransplanted s.c. formed a well-differentiated ductal adenocarcinoma. CONCLUSIONS: Pancreatic β-cells are the primary target of BOP without necessarily being embedded in the compound of the Langerhans' islet. With time in culture, they give rise to undifferentiated cells and after malignant transformation they are able to form ductal adenocarcinoma.
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Authors | S A Müller, K Bläuer, G Ergin, F Bergmann, K Z'graggen, B M Schmied, A Ulrich |
Journal | Pancreatology : official journal of the International Association of Pancreatology (IAP) ... [et al.]
(Pancreatology)
2012 Jul-Aug
Vol. 12
Issue 4
Pg. 380-7
ISSN: 1424-3911 [Electronic] Switzerland |
PMID | 22898641
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Copyright | Copyright © 2012 IAP and EPC. Published by Elsevier B.V. All rights reserved. |
Chemical References |
- Carcinogens
- Nitrosamines
- nitrosobis(2-oxopropyl)amine
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Topics |
- Adenocarcinoma
(chemically induced, pathology)
- Animals
- Carcinogens
- Carcinoma, Pancreatic Ductal
(chemically induced, pathology)
- Cell Line, Tumor
- Cell Proliferation
- Cell Separation
- Cell Transformation, Neoplastic
(chemically induced)
- Cells, Cultured
- Cricetinae
- Female
- Insulin-Secreting Cells
(drug effects, pathology)
- Mesocricetus
- Neoplasm Invasiveness
(pathology)
- Neoplasm Transplantation
- Nitrosamines
(toxicity)
- Pancreatic Neoplasms
(chemically induced, pathology)
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