Source:http://linkedlifedata.com/resource/pubmed/id/20361349
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
2
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pubmed:dateCreated |
2010-11-18
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pubmed:abstractText |
Interleukin-6 (IL-6) is a growth and survival factor in human glioblastoma cells and plays an important role in malignant progression. However, its role in glioblastoma invasion is still unknown. This study shows how IL-6 promotes cell invasion and migration in U251 and T98G glioblastoma cell lines. The underlying mechanism includes both protease-dependent and -independent manners. Stimulation with IL-6 increased MMP9 expression in the two cell lines but had no influence on MMP2 expression. Fascin-1 is a cell skeleton binding protein and plays a key role in cell migration and invasion. Its binding style directly influences cell morphology and tendency to become deformed. After IL-6 exposure, fascin-1 expression increased in an IL-6 dose-dependent manner. Immunofluorescence also revealed that the binding style of fascin-1 had changed after IL-6 exposure, resulting in a more invasive phenotype of the cells. Three most commonly emphasized invasion-associated signaling pathways, including JAK-STAT3, p42/44 MAPK, and PI3K/AKT, were verified to further illustrate its underlying mechanism. Only phosphorylation of STAT3 at ser 727 site paralleled the IL-6 stimulation, and JSI-124, a specific JAK-STAT3 pathway blocker, deterred the invasion and migration promotive effect of IL-6, indicating that the JAK/STAT3 pathway mediates signal transduction. Furthermore, IL-6 also acts in a paracrine fashion to promote vascular endothelial cell migration, thus facilitating tumor angiogenesis and invasion. These results suggest that IL-6 promotes glioblastoma cell invasion and angiogenesis and may be a potential anti-invasion target.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Carrier Proteins,
http://linkedlifedata.com/resource/pubmed/chemical/FSCN1 protein, human,
http://linkedlifedata.com/resource/pubmed/chemical/IL6 protein, human,
http://linkedlifedata.com/resource/pubmed/chemical/Interleukin-6,
http://linkedlifedata.com/resource/pubmed/chemical/Microfilament Proteins
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pubmed:status |
MEDLINE
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pubmed:month |
Nov
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pubmed:issn |
1573-7373
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pubmed:author | |
pubmed:issnType |
Electronic
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pubmed:volume |
100
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
165-76
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pubmed:meshHeading |
pubmed-meshheading:20361349-Brain Neoplasms,
pubmed-meshheading:20361349-Carrier Proteins,
pubmed-meshheading:20361349-Cell Line, Tumor,
pubmed-meshheading:20361349-Cell Movement,
pubmed-meshheading:20361349-Fluorescent Antibody Technique,
pubmed-meshheading:20361349-Glioblastoma,
pubmed-meshheading:20361349-Humans,
pubmed-meshheading:20361349-Immunoblotting,
pubmed-meshheading:20361349-Interleukin-6,
pubmed-meshheading:20361349-Microfilament Proteins,
pubmed-meshheading:20361349-Neoplasm Invasiveness,
pubmed-meshheading:20361349-Neovascularization, Pathologic,
pubmed-meshheading:20361349-Reverse Transcriptase Polymerase Chain Reaction,
pubmed-meshheading:20361349-Signal Transduction
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pubmed:year |
2010
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pubmed:articleTitle |
IL-6 promotion of glioblastoma cell invasion and angiogenesis in U251 and T98G cell lines.
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pubmed:affiliation |
Department of Neurosurgery, Qi Lu Hospital, Shandong University, Wenhua Xi Road, Jinan, Shandong, People's Republic of China.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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