Source:http://linkedlifedata.com/resource/pubmed/id/19018771
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
12
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pubmed:dateCreated |
2008-12-16
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pubmed:abstractText |
The irradiated fibroblast-induced response of non-irradiated neighboring cells is called 'radiation-induced bystander effect', but it is unclear in non-irradiated human squamous cell carcinoma (SCC) cells. The present study shows that irradiated fibroblasts promoted the invasive growth of T3M-1 SCC cells, but not their apoptosis, more greatly than non-irradiated fibroblasts, using collagen gel invasion assay, immunohistochemistry and Western blot. The number of irradiated fibroblasts decreased to about 30% of that of non-irradiated fibroblasts, but irradiated fibroblasts increased the growth marker ki-67 display of SCC cells more greatly than non-irradiated fibroblasts. Irradiated fibroblasts did not affect the apoptosis marker ss-DNA expression of SCC cells. Irradiated fibroblasts enhanced the display of the following growth-, invasion- and motility-related molecules in SCC cells more greatly than non-irradiated fibroblasts: c-Met, Ras, mitogen-activated protein kinase (MAPK) cascade (Raf-1, MEK-1 and ERK-1/2), matrix metalloproteinase-1 and -9, laminin 5 and filamin A. Irradiated fibroblasts, but not non-irradiated ones, formed irradiation-induced foci (IRIF) of the genomic instability marker p53-binding protein 1 (53BP1) and expressed transforming growth factor-beta1 (TGF- beta1). Irradiated fibroblasts in turn enabled SCC cells to enhance 53BP1 IRIF formation more extensively than non-irradiated fibroblasts. Finally, effects of irradiated fibroblasts on growth and apoptosis of another HEp-2 SCC cell type were similar to those of T3M-1. These results suggest that irradiated fibroblasts promotes invasion and growth of SCC cells by enhancement of invasive growth-related molecules above through TGF- beta1-mediated bystander mechanism, in which irradiated fibroblast-induced genomic instability of SCC cells may be involved.
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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 |
1349-7006
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pubmed:author | |
pubmed:issnType |
Electronic
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pubmed:volume |
99
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
2417-27
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pubmed:meshHeading |
pubmed-meshheading:19018771-Animals,
pubmed-meshheading:19018771-Bystander Effect,
pubmed-meshheading:19018771-Carcinoma, Squamous Cell,
pubmed-meshheading:19018771-Cell Line, Tumor,
pubmed-meshheading:19018771-Cell Proliferation,
pubmed-meshheading:19018771-Dose-Response Relationship, Radiation,
pubmed-meshheading:19018771-Fibroblasts,
pubmed-meshheading:19018771-Humans,
pubmed-meshheading:19018771-Immunohistochemistry,
pubmed-meshheading:19018771-Ki-67 Antigen,
pubmed-meshheading:19018771-Mice,
pubmed-meshheading:19018771-Mouth Neoplasms,
pubmed-meshheading:19018771-NIH 3T3 Cells,
pubmed-meshheading:19018771-Neoplasm Invasiveness,
pubmed-meshheading:19018771-Neoplasms,
pubmed-meshheading:19018771-Stromal Cells
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pubmed:year |
2008
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pubmed:articleTitle |
Irradiated fibroblast-induced bystander effects on invasive growth of squamous cell carcinoma under cancer-stromal cell interaction.
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pubmed:affiliation |
Department of Pathology & Biodefense, Faculty of Medicine, Saga University, Saga 849-8501, Japan.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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