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- Title
Expression of a dominant negative type II TGF-β receptor in mouse skin results in an increase in carcinoma incidence and an acceleration of carcinoma development.
- Authors
Amendt, C; Schirmacher, P; Weber, H; Blessing, M
- Abstract
The role of Transforming growth factor beta (TGF-β) in carcinogenesis is complex. There are reports on both tumor inhibition and tumor promotion by TGF-β. To elucidate the complex role of TGF-β in epithelial carcinogenesis, we generated transgenic mice overexpressing a dominant negative type II TGF-β receptor in the basal cell compartment and in follicular cells of the skin. Despite the reduced responsiveness of transgenic keratinocytes to TGF-β, both proliferation and differentiation were normal in non-irritated epidermis of these transgenic mice. Thus, interruption of signaling of all three isoforms of TGF-β in basal and follicular cells does not disturb tissue homeostasis. However, during tumor promotion transgenic mice showed an elevated level of proliferation in the epidermis. This hyperproliferation correlated with a very early onset of carcinoma development and a malignant conversion frequency of 30% from benign papillomas to carcinomas. By comparison, the conversion frequency in wild-type mice of this strain has previously been reported as 5.5%. Even without induction of hyperproliferation by tumor promoters, transgenic mice developed far more carcinomas as controls when treated with a carcinogen. This result indicates that there is a synergistic effect between loss of TGF-β responsiveness and mutations caused by initiation with a carcinogen leading to an endogeneous tumor promotion in initiated cells only.
- Subjects
MICE; SKIN; TRANSFORMING growth factors-beta; ANIMAL models of carcinogenesis
- Publication
Oncogene, 1998, Vol 17, Issue 1, p25
- ISSN
0950-9232
- Publication type
Article
- DOI
10.1038/sj.onc.1202161