E2F1 suppresses skin carcinogenesis via the ARF-p53 pathway

JL Russell, RL Weaks, TR Berton, DG Johnson - Oncogene, 2006 - nature.com
JL Russell, RL Weaks, TR Berton, DG Johnson
Oncogene, 2006nature.com
The E2F1 transcription factor, which is deregulated in most human cancers by mutations in
the p16-cyclin D-Rb pathway, has both oncogenic and tumor-suppressive properties. This is
dramatically illustrated by the phenotype of an E2F1 transgenic mouse model that
spontaneously develops tumors in the skin and other epithelial tissues but is resistant to
papilloma formation when subjected to a two-stage carcinogenesis protocol. Here, this E2F1
transgenic model was used to further explore the tumor-suppressive property of E2F1 …
Abstract
The E2F1 transcription factor, which is deregulated in most human cancers by mutations in the p16-cyclin D-Rb pathway, has both oncogenic and tumor-suppressive properties. This is dramatically illustrated by the phenotype of an E2F1 transgenic mouse model that spontaneously develops tumors in the skin and other epithelial tissues but is resistant to papilloma formation when subjected to a two-stage carcinogenesis protocol. Here, this E2F1 transgenic model was used to further explore the tumor-suppressive property of E2F1. Transgenic expression of E2F1 was found to inhibit ras-driven skin carcinogenesis at the promotion stage independent of the type of promoting agent used. E2F1 transgenic epidermis displayed increased expression of p19 ARF, p53, and p21 Cip1. Inactivation of either p53 or Arf in E2F1 transgenic mice restored sensitivity to two-stage skin carcinogenesis. While Arf inactivation impaired tumor suppression and p21 induction by E2F1, it did not reduce the level of apoptosis observed in E2F1 transgenic mice. Based on these findings, we propose that E2F1 suppresses ras-driven skin carcinogenesis through a nonapoptotic mechanism involving ARF and p53.
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