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pubmed-article:12054346pubmed:abstractTextThe PEA3 group members PEA3, ER81 and ERM, which are highly conserved transcription factors from the Ets family, are over-expressed in metastatic mammary tumors. In the current study, we present the characterization of a transgenic mouse strain which over-expresses ER81 in the mammary gland via the long terminal repeat of the mouse mammary tumor virus (LTR-MMTV). Although six genotypically positive transgenic lines were identified, only one expressed the ectopic transcript with an exclusive expression in the lactating and late-pregnancy (18th day) mammary glands. No mammary tumor or mammary deregulation appeared after 2 years of ectopic ER81 expression following lactation. We then sought to identify ER81 target genes, and the urokinase plasminogen activator (uPA) and the stromelysin-1, two enzymes involved in extracellular matrix degradation, were found to be transcriptionally upregulated in lactating mammary glands over-expressing ER81. Since these enzymes are involved in metastasis, this murine model could be further used to enhance mammary cancer metastatic process by crossing these animals with mice carrying non-metastatic mammary tumors. We thus created a transgenic mouse model permitting the over-expression of a functionally active Ets transcription factor in the mammary gland without perturbing its development.lld:pubmed
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pubmed-article:12054346pubmed:pagination123-31lld:pubmed
pubmed-article:12054346pubmed:dateRevised2008-11-21lld:pubmed
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pubmed-article:12054346pubmed:articleTitleEctopic expression of the ets transcription factor ER81 in transgenic mouse mammary gland enhances both urokinase plasminogen activator and stromelysin-1 transcription.lld:pubmed
pubmed-article:12054346pubmed:affiliationUMR 8526 CNRS, Institut de Biologie de Lille, Institut Pasteur de Lille, France.lld:pubmed
pubmed-article:12054346pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:12054346pubmed:publicationTypeResearch Support, Non-U.S. Gov'tlld:pubmed
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