Transcriptomic analysis were performed by Taqman LDA technology. Tumor growth in vivo was analyzed in NOD/SCID mice. We have observed that primary human lung tumors express TLR3, TLR4, TLR7 and TLR8 and that stimulation of these receptors in lung tumor cell lines by Poly I:C, LPS, Loxoribine or Poly U induces NFκB activation through atypical learn more signaling pathway, with phosphorylation of IκBα without its degradation and nuclear translocation of p50 and p65 NFκB subunits. Interestingly, we observed

that TLR3 stimulation induces apoptosis. On the contrary TLR4, TLR7 and TLR8 stimulation induces cell survival and increases clonogenicity. Moreover, despite a common atypical activation of NFκB, our transcriptomic analysis revealed major differences in gene modulation after triggering of TLR3,

TLR4, TLR7 and TLR8. Finally, in vivo TLR7 stimulation of human lung tumor cells dramatically increases tumor growth. Altogether, these data emphasize that TLR4, TLR7 or TLR8 triggering can directly favor tumor development whereas TLR3 signaling can induce tumor cell death. These data suggest that anticancer immunotherapy using TLR adjuvants should take into account the expression of these TLRs in lung tumor cells. Poster No. 63 Elastin-Derived Peptides: Matrikines Critical for Glioblastoma Cell Aggressiveness in a 3-D System Berenice Coquerel 1 , Francois Proust2, Georges Bellon3, Jean-Pierre Vannier1 1 Faculté Alvelestat mouse de Médecine de Rouen, Laboratoire MERCI UPRES EA 3829, Rouen, France, 2 Department of Neurosurgery, CHU de Rouen, Rouen, France, 3 Faculté de Médecine de Reims, Laboratoire de Biochimie et Biologie Moléculaire,

UMR 6237 CNRS, Reims, France In the most common primary brain tumors, malignant glioma cells invade the extra-cellular matrix (ECM) and proliferate rapidly in the cerebral tissue which is mainly composed of hyaluronan (HA) along with the elastin present in the basement membrane of blood vessels. To determine the role of ECM components in the invasive capacity of glioma cell lines, we developed a 3-D cell culture system, based on a hydrogel in which HA can be co-reticulated with kappa-Elastin (HA-kE). Using this system, the Nintedanib (BIBF 1120) invasiveness of cells from four glioma cell lines was dramatically increased by the presence of kE and a related, specific peptide (VGVAPG)3 (see figure 1 A and B). In addition, MMP-2 secretion increased and MMP-12 synthesis occurred. Extracellular injections of kE or (VGVAPG)3 provoked a pronounced, and dose-dependent increase in [Ca2+]i. kE significantly enhanced expression of the genes encoding elastin-receptor and tropoelastin, the migration (see figure 2 A and B), the adhesion and the proliferation of the glioma cells. We propose the existence of a positive feedback loop in which degradation of elastin generates fragments that stimulate synthesis of tropoelastin followed by further degradation as well as migration and proliferation of the very cells responsible for degradation.