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Cyclin D1 is not an immediate target of beta-catenin following Apc loss in the intestine.

Sansom, O.J. and Reed, K.R. and Wetering, M.van de and Muncan, V. and Winston, D. and Clevers, J.C. and Clarke, A.R. (2005) Cyclin D1 is not an immediate target of beta-catenin following Apc loss in the intestine. The Journal of biological chemistry, 280(31), 28463-28467. ISSN 00219258. doi: 10.1074/jbc.M500191200.

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Abstract

Cyclin D1 is postulated to be a target of the canonical Wnt pathway and critical for intestinal adenoma development. We show here that, unlike cyclin D1 reporter assays, endogenous cyclin D1 levels are not affected following antagonism of the Wnt pathway in vitro, nor is cyclin D1immediately up-regulated following conditional loss of Apc in vivo. Cyclin D1 levels do, however, increase in a delayed manner in a small subset of cells, suggesting such up-regulation occurs as a secondary event. We also analyzed the immediate consequences of Apc loss in a cyclin D1(-/-) background and failed to find any cyclin D1-dependent phenotypes. However, we did observe elevated cyclin D1 expression in lesions developing 20 days after Apc loss. In these circumstances, all adenomas (but not smaller lesions) showed cyclin D1 up-regulation. Finally in a smaller study, we analyzed whether cyclin D1 deficiency affected adenoma formation 20 days following induced loss of Apc. Unlike AhCre(+) Apc(fl/fl) mice (which all developed adenomas), doubly mutant AhCre(+) Apc(fl/fl) cyclin D1(-/-) mice only developed small lesions. Taken together, this argues that cyclin D1up-regulation in intestinal neoplasia is important for tumor progression rather than initiation.

Item Type:Article
Additional Information:doi: 10.1074/jbc.M500191200
Institutes:Hubrecht Instituut
ID Code:3610
Deposited On:13 Feb 2009 17:14
Last Modified:10 Dec 2009 13:14

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