Your browser doesn't support javascript.
loading
Show: 20 | 50 | 100
Results 1 - 1 de 1
Filter
Add more filters










Database
Language
Publication year range
1.
Cancer Cell ; 13(3): 235-48, 2008 Mar.
Article in English | MEDLINE | ID: mdl-18328427

ABSTRACT

Invasion of surrounding brain tissue by isolated tumor cells represents one of the main obstacles to a curative therapy of glioblastoma multiforme. Here we unravel a mechanism regulating glioma infiltration. Tumor interaction with the surrounding brain tissue induces CD95 Ligand expression. Binding of CD95 Ligand to CD95 on glioblastoma cells recruits the Src family member Yes and the p85 subunit of phosphatidylinositol 3-kinase to CD95, which signal invasion via the glycogen synthase kinase 3-beta pathway and subsequent expression of matrix metalloproteinases. In a murine syngeneic model of intracranial GBM, neutralization of CD95 activity dramatically reduced the number of invading cells. Our results uncover CD95 as an activator of PI3K and, most importantly, as a crucial trigger of basal invasion of glioblastoma in vivo.


Subject(s)
Brain Neoplasms/metabolism , Fas Ligand Protein/metabolism , Glioblastoma/metabolism , Phosphatidylinositol 3-Kinases/metabolism , Proto-Oncogene Proteins c-yes/metabolism , Signal Transduction , fas Receptor/metabolism , Animals , Apoptosis , Brain Neoplasms/enzymology , Brain Neoplasms/genetics , Brain Neoplasms/immunology , Brain Neoplasms/pathology , Cell Line, Tumor , Cell Movement , Death Domain Receptor Signaling Adaptor Proteins/metabolism , Glioblastoma/enzymology , Glioblastoma/genetics , Glioblastoma/immunology , Glioblastoma/pathology , Glycogen Synthase Kinase 3/metabolism , Glycogen Synthase Kinase 3 beta , Humans , Matrix Metalloproteinases/genetics , Matrix Metalloproteinases/metabolism , Mice , Neoplasm Invasiveness , Neoplasm Transplantation , Proto-Oncogene Proteins c-yes/genetics , RNA Interference , RNA, Small Interfering/metabolism , Recombinant Fusion Proteins/metabolism , Transfection , Transplantation, Isogeneic , Tumor Cells, Cultured , src-Family Kinases/metabolism
SELECTION OF CITATIONS
SEARCH DETAIL
...