Reference : Radiation enhances the invasive potential of primary glioblastoma cells via activatio...
Scientific journals : Article
Life sciences : Genetics & genetic processes
http://hdl.handle.net/2268/84336
Radiation enhances the invasive potential of primary glioblastoma cells via activation of the Rho signaling pathway.
English
Zhai, Gary G [> > > >]
Malhotra, Rajeev [> > > >]
Delaney, Meaghan [> > > >]
Latham, Douglas [> > > >]
Nestler, Ulf [> > > >]
Zhang, Min [> > > >]
Mukherjee, Neelanjan [> > > >]
Song, Qinhui [> > > >]
Robe, Pierre mailto [Université de Liège - ULg > Département des sciences biomédicales et précliniques > Génétique générale et humaine - Département des sciences biomédicales et précliniques >]
Chakravarti, Arnab [> > > >]
2006
Journal of neuro-oncology
76
3
227-37
Yes
International
0167-594X
Netherlands
[en] 1-Phosphatidylinositol 3-Kinase/metabolism/radiation effects ; Animals ; Blotting, Western ; Brain Neoplasms/pathology ; Cell Line, Tumor ; Enzyme Activation/radiation effects ; Glioblastoma/pathology ; Humans ; Male ; Neoplasm Invasiveness ; Radiation Tolerance/physiology ; Rats ; Rats, Inbred F344 ; Receptor, Epidermal Growth Factor/metabolism/radiation effects ; Receptor, IGF Type 1/metabolism/radiation effects ; Signal Transduction/physiology ; Transfection ; rho GTP-Binding Proteins/metabolism/radiation effects
[en] Glioblastoma multiforme (GBM) is among the most treatment-refractory of all human tumors. Radiation is effective at prolonging survival of GBM patients; however, the vast majority of GBM patients demonstrate progression at or near the site of original treatment. We have identified primary GBM cell lines that demonstrate increased invasive potential upon radiation exposure. As this represents a novel mechanism by which radiation-treated GBMs can fail therapy, we further investigated the identity of downstream signaling molecules that enhance the invasive phenotype of irradiated GBMs. Matrigel matrices were used to compare the extent of invasion of irradiated vs. non-irradiated GBM cell lines UN3 and GM2. The in vitro invasive potential of these irradiated cells were characterized in the presence of both pharmacologic and dominant negative inhibitors of extracellular matrix and cell signaling molecules including MMP, uPA, IGFR, EGFR, PI-3K, AKT, and Rho kinase. The effect of radiation on the expression of these signaling molecules was determined with Western blot assays. Ultimately, the in vitro tumor invasion results were confirmed using an in vivo 9L GBM model in rats. Using the primary GBM cell lines UN3 and GM2, we found that radiation enhances the invasive potential of these cells via activation of EGFR and IGFR1. Our findings suggest that activation of Rho signaling via PI-3K is required for radiation-induced invasion, although not required for invasion under physiologic conditions. This report clearly demonstrates that radiation-mediated invasion is fundamentally distinct from invasion under normal cellular physiology and identifies potential therapeutic targets to overcome this phenomenon.
http://hdl.handle.net/2268/84336
10.1007/s11060-005-6499-4

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