While we observed these expression changes in the fibroblasts in response to the genotype of the epithelial cells, we also identified

reciprocal changes in the epithelial cells themselves: Gene expression analysis of invasive and non-invasive areas of ECdnT cells in the organotypic epithelial reconstruct cultures identified AP26113 concentration cathepsin B and CD44 to be upregulated in invasive cells. The increase of cathepsin B expression in ECdnT cells appears to be an upstream event in the signaling cascade culminating in cell invasion, as cathepsin B can cleave and activate TGFβ1. CD44 activation is in part mediated through TGFβ1. We show then, that CD44 co-localizes with MMP-2 and MMP-9 to invasive areas and facilitates matrix degradation allowing for cell invasion into the underlying collagen/matrigel layer. In summary, we demonstrate here that the epithelial loss of E-cadherin and TβRII leads to an impaired balance of the epithelial-mesenychmal crosstalk resulting BMN 673 in vitro in the

activation of fibroblasts and the induction of invasion through a fibroblast-secreted factor. O38 Cancer-Associated Adipocytes: New Key Players in Breast Tumour Invasion Béatrice Dirat1,2, Ghislaine Escourrou3, Stéphanie Dauvillier1, Ludivine Bochet1,2, Philippe Valet2, Catherine Muller 1 1 Microenvironment, Cancer and Adipocytes (MICA), IPBS-CNRS UMR 5089, Toulouse, France, 2 AdipOlab, INSERM U858- Team 3, I2MR, Toulouse, France, 3 Laboratoire d’Anatomie Pathologie et Histologie, Centre click here Hospitalier Universitaire Rangueil, Toulouse, France Most of the studies on epithelial-stroma interactions during breast cancer cell invasion have focused on fibroblasts, endothelial and inflammatory cells. Very little attention has been given to adipocytes, although it is obvious that in numerous organs including breast, early local tumour invasion results in immediate proximity of cancer cells to adipocytes. Until recently, adipocytes were considered as an energy storage depot, but there is now clear evidence that their ability to secrete many adipokines could

potentially influence tumour behaviour. Using an original 2D co-culture system where adipocytes and tumour cell are separated by an insert, we show a crosstalk between the two cell types. Tumour co-cultivated during 3 to 5 days with adipocytes exhibit Rutecarpine an increase in both migratory and invasive capacities and incomplete EMT. This pro-invasive effect was not recapitulated with “naïve” adipocyte-conditioned medium (Ad-CM), but was recapitulated when tumour cells were grown in the presence of Ad-CM obtained from adipocytes previously grown in the presence of cancer cells. In fact, adipocytes cultivated with cancer cells exhibit profound changes with delipidation and decreased of adipocyte markers associated to a concomitant expression of an activated phenotype marked by overexpression of proteases (including MMP-11) and pro-inflammatory cytokines (IL-6, Il-1β).

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