Source:http://linkedlifedata.com/resource/pubmed/id/21852034
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
2
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pubmed:dateCreated |
2011-9-29
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pubmed:abstractText |
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.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
Dec
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pubmed:issn |
1872-7980
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pubmed:author | |
pubmed:copyrightInfo |
Copyright © 2011 Elsevier Ireland Ltd. All rights reserved.
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pubmed:issnType |
Electronic
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pubmed:day |
8
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pubmed:volume |
311
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
195-202
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pubmed:meshHeading |
pubmed-meshheading:21852034-Antigens, CD95,
pubmed-meshheading:21852034-Cell Line, Tumor,
pubmed-meshheading:21852034-Cell Movement,
pubmed-meshheading:21852034-Cell Proliferation,
pubmed-meshheading:21852034-Glioblastoma,
pubmed-meshheading:21852034-Humans,
pubmed-meshheading:21852034-Immunohistochemistry,
pubmed-meshheading:21852034-Matrix Metalloproteinase 9,
pubmed-meshheading:21852034-Signal Transduction,
pubmed-meshheading:21852034-Toll-Like Receptor 4
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pubmed:year |
2011
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pubmed:articleTitle |
TLR4 signal transduction pathways neutralize the effect of Fas signals on glioblastoma cell proliferation and migration.
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pubmed:affiliation |
EA 3842 (Homéostasie Cellulaire et Pathologies), Institut Fédératif de Recherche 145, Facultés de Médecine et de Pharmacie, Université de Limoges, Limoges, France.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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