The actors of human implantation: gametes, embryo and endometriumGridelet, Virginie ; GASPARD, Olivier ; Polese, Barbara et alin Violin Pereira, Luis Antonio (Ed.) Embryology - Updates and Highlights on Classic Topics (2012) Detailed reference viewed: 9 (2 ULg) CERTOLIZUMAB PEGOL DID NOT RESULT IN A DECREASE IN SEMEN QUALITY IN HEALTHY VOLUNTEERS: RESULTS FROM A PHASE 1 STUDYPerrier d'Hauterive, Sophie ; KESSELER, Sophie ; RUGGERI, Philippe et alin EULAR 2012 (2012) Detailed reference viewed: 8 (0 ULg) Transactivation of vimentin by beta-catenin in human breast cancer cellsGilles, Christine ; ; Mestdagt, Mélanie et alin Cancer Research (2003), 63(10), 2658-2664 The cytoplasmic and nuclear redistribution of beta-catenin and the de novo expression of vimentin are frequently involved in the epithelial-to-mesenchymal transition associated with increased invasive ... [more ▼] The cytoplasmic and nuclear redistribution of beta-catenin and the de novo expression of vimentin are frequently involved in the epithelial-to-mesenchymal transition associated with increased invasive/migratory properties of epithelial cells. Because beta-catenin can act as a coactivator of transcription through its binding to the T-cell factor (TCF)/lymphoid enhancer factor 1 transcription factor family, we have explored the possibility that beta-catenin/TCF could directly transactivate vimentin. We first compared vimentin expression in relation with the localization of beta-catenin in eight breast cancer cell lines displaying various degrees of invasiveness and in a model of cell migration using human mammary MCF10A cells. We could thus show a cytoplasmic and/or nuclear distribution of beta-catenin in invasive/migratory cells expressing vimentin, but not in noninvasive/stationary vimentin-negative cell lines. In addition, the human vimentin promoter was found to be up-regulated by beta-catenin and TCF-4 cotransfection. Varying with the cellular background, a diminution of this up-regulation was observed when the putative beta-catenin/TCF binding site of the vimentin promoter was mutated. Our results therefore demonstrate that the vimentin promoter is a target of the beta-catenin/TCF pathway and strongly suggest an implication of this regulation in epithelial cell migration/invasion. [less ▲] Detailed reference viewed: 50 (4 ULg) |
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