Breast Cancer Research

official impact factor 5.79

Open Access Research article

PAI-1 and functional blockade of SNAI1 in breast cancer cell migration

Elizabeth Fabre-Guillevin1,2, Michel Malo1, Amandine Cartier-Michaud1, Hector Peinado3, Gema Moreno-Bueno4, Benoît Vallée1,6, Daniel A Lawrence5, José Palacios4, Amparo Cano3, Georgia Barlovatz-Meimon1,6* and Cécile Charrière-Bertrand1,6

Author Affiliations

1 DYNAMIC Team, IBISC FRE 3190 CNRS – Université d'Evry Val d'Essonne, Genopole, Evry 91000, France

2 Department of Medical Oncology, Hopital Européen Georges Pompidou, Paris cedex 15 75908, France

3 Departamento de Bioquímica, Instituto de Investigaciones Biomedicas 'Alberto Sols', (CSIC-UAM), Madrid 28029, Spain

4 Molecular Pathology Program, Centro Nacional de Investigaciones Oncologicas (CNIO), Madrid 28029, Spain

5 Department of Internal Medicine, University of Michigan School of Medicine, Ann Arbor MI 48109-0644, USA

6 University Paris 12 – Val de Marne, Créteil cedex 94010, France

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Breast Cancer Research 2008, 10:R100 doi:10.1186/bcr2203

Published: 3 December 2008

Additional files

Additional data file 1:

A table that lists the human genes up-regulated or down-regulated in a clone expressing a dominant-negative form of SNAI1 (SNAI1-DN) compared with MDA-mock control cells. Negative sign (-) means down-regulation and positive sign (+) means up-regulation. Genes are organised by molecular function. A total of 99 genes were found to be differentially expressed, by at least a two-fold factor, in response to SNAI1 functional blockade.

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