کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
2113468 | 1084470 | 2011 | 8 صفحه PDF | دانلود رایگان |

The Fas pathway is described as an activator of the glioblastoma proliferation by increasing the pathogenicity of this tumour. The lipopolysaccharide (LPS) pathway depending on Toll-like receptor 4 (TLR4) could limit the glioblastoma spreading. Here, Fas and TLR4 pathways were activated in glioblastoma cell lines by an agonist antibody and/or LPS treatment. Activation of the Fas pathway or of the TLR4 pathway induced cell proliferation. However, simultaneous treatment with agonist antibody and LPS decreased proliferation. This anti-proliferative effect was caspase dependent, and a decreased cell migration and matrix metalloproteinase (MMP)-9 expression were also observed. Both TLR4 and MMP-9 were highly expressed in human glioblastoma tissues. These data suggest that TLR4 signal transduction pathways neutralize proliferation and migration induced by Fas pathway activation in glioblastoma cell lines.
► Fas or TLR4 (LPS receptor) pathway activation induces glioblastoma cell proliferation.
► Simultaneous cell treatment by Fas agonist antibody and LPS decreases proliferation.
► This anti-proliferative effect is caspase dependent.
► This treatment decreases cell migration and MMP-9 expression.
► Both TLR4 and MMP-9 are highly expressed in human glioblastomas.
Journal: Cancer Letters - Volume 311, Issue 2, 8 December 2011, Pages 195–202