TY - JOUR
T1 - Time-sensitive reversal of hyperplasia in transgenic mice expressing SV40 T antigen
AU - Ewald, Dagmar
AU - Li, Minglin
AU - Efrat, Shimon
AU - Auer, Gert
AU - Wall, Robert J.
AU - Furth, Priscilla A.
AU - Hennighausen, Lothar
N1 - Funding Information:
We are very grateful to Norbert Schäffer, Frank Vassen, Gerard Rocamora, Glen Tyler, Gillian Gilbert and Dave Hodson who provided recordings and Phil Benstead, Cath Jeffs and Alex Turner for help and hospitality in the Outer Hebrides. Ken Smith and Rhys Green provided fruitful discussion on various aspects of this study. Paolo Galeotti and three anonymous referees provided comments that improved the manuscript. T.M. Peake was supported by a Biotechnology and Biological Sciences Research Council studentship with the Royal Society for the Protection of Birds. Analysis equipment was funded by the Natural Environment Research Council and the Royal Society.
PY - 1996/9/6
Y1 - 1996/9/6
N2 - The role of viral oncoprotein expression in the maintenance of cellular transformation was examined as a function of time through controlled expression of simian virus 40 T antigen (TAg). Expression of TAg in the submandibular gland of transgenic mice from the time of birth induced cellular transformation and extensive ductal hyperplasia by 4 months of age. The hyperplasia was reversed when TAg expression was silenced for 3 weeks. When TAg expression was silenced after 7 months, however, the hyperplasia persisted even though TAg was absent. Although the polyploidy of ductal cells could be reversed at 4 months of age, cells at 7 months of age remained polyploid even in the absence of TAg. These results support a model of time- dependent multistep tumorigenesis, in which virally transformed cells eventually lose their dependence on the viral oncoprotein for maintenance of the transformed state.
AB - The role of viral oncoprotein expression in the maintenance of cellular transformation was examined as a function of time through controlled expression of simian virus 40 T antigen (TAg). Expression of TAg in the submandibular gland of transgenic mice from the time of birth induced cellular transformation and extensive ductal hyperplasia by 4 months of age. The hyperplasia was reversed when TAg expression was silenced for 3 weeks. When TAg expression was silenced after 7 months, however, the hyperplasia persisted even though TAg was absent. Although the polyploidy of ductal cells could be reversed at 4 months of age, cells at 7 months of age remained polyploid even in the absence of TAg. These results support a model of time- dependent multistep tumorigenesis, in which virally transformed cells eventually lose their dependence on the viral oncoprotein for maintenance of the transformed state.
UR - http://www.scopus.com/inward/record.url?scp=0029818753&partnerID=8YFLogxK
U2 - 10.1126/science.273.5280.1384
DO - 10.1126/science.273.5280.1384
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AN - SCOPUS:0029818753
SN - 0036-8075
VL - 273
SP - 1384
EP - 1386
JO - Science
JF - Science
IS - 5280
ER -