The transcription factor, early growth response protein 1 (ECR1), is overex
pressed in a majority of human prostate cancers and is implicated in the re
gulation of several genes important for prostate tumor progression. Here we
have assessed the effect of Egr1 deficiency on tumor development in two tr
ansgenic mouse models of prostate cancer (CR2-T-Ag and TRAMP). Using a comb
ination of high-resolution magnetic resonance imaging and histopathological
and survival analyses, we show that tumor progression was significantly im
paired in Egr1(-/-) mice. Tumor initiation and tumor growth rate were not a
ffected by the lack of Egr1; however, Egr1 deficiency significantly delayed
the progression from prostatic intra-epithelial neoplasia to invasive carc
inoma. These results indicate a unique role for Egr1 in regulating the tran
sition from localized, carcinoma in situ to invasive carcinoma.