Source:http://linkedlifedata.com/resource/pubmed/id/17671690
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
3
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pubmed:dateCreated |
2007-8-2
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pubmed:abstractText |
While the effects of single growth factors on endothelial cells (ECs) have been extensively studied, the importance of induction of growth factors such as PDGF-BB (platelet derived growth factor) in ECs and its impact on tumor cell functions are only partly understood. Human umbilical vein endothelial cells (HUVECs) were cultured under serum-free conditions and stimulated by 20 ng/ml VEGF (vascular endothelial growth factor) or 20 ng/ml bFGF (basic fibroblastic growth factor). As determined by real-time PCR, both VEGF and bFGF induced a significant (up to 4-fold) increase in PDGF-B RNA expression which was time- and dose-dependent (p<0.05). Similarly, conditioned medium (CM) from lung cancer cells (A549) which is known to contain multiple growth factors including VEGF and bFGF also induced PDGF-B RNA expression. Using ELISA assays, VEGF and bFGF significantly increased PDGF-BB protein secretion in HUVECs (p<0.01). By addition of BIBF 1000, a novel inhibitor of the VEGF and bFGF receptor kinases, the effect of VEGF on PDGF-B RNA induction was significantly antagonized (p<0.01). Furthermore, we studied the biological significance of EC-derived PDGF-BB on lung cancer cells. Interestingly, HUVEC-derived CM significantly stimulated migration of A549 cells (p<0.001) with a trend to further increased migration with the use of VEGF-stimulated (PDGF-BB rich) CM (p=0.2). Collectively, endothelial and lung cancer cells seem to interact via various paracrine pathways, e.g. by the reciprocal induction of VEGF and PDGF-BB. Thus, targeting key molecules would result in expression alterations of multiple factors and alter the biological functions of both stromal and tumor cells.
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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/BIBF 1000,
http://linkedlifedata.com/resource/pubmed/chemical/Indoles,
http://linkedlifedata.com/resource/pubmed/chemical/Platelet-Derived Growth Factor,
http://linkedlifedata.com/resource/pubmed/chemical/RNA,
http://linkedlifedata.com/resource/pubmed/chemical/Recombinant Proteins,
http://linkedlifedata.com/resource/pubmed/chemical/Vascular Endothelial Growth Factor A,
http://linkedlifedata.com/resource/pubmed/chemical/platelet-derived growth factor BB
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pubmed:status |
MEDLINE
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pubmed:month |
Sep
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pubmed:issn |
1019-6439
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pubmed:author |
pubmed-author:BerdelWolfgangW,
pubmed-author:BispingGuidoG,
pubmed-author:FehrmannNicoleN,
pubmed-author:HilbergFrankF,
pubmed-author:KesslerTorstenT,
pubmed-author:MestersRolf MRM,
pubmed-author:RaedelMiriamM,
pubmed-author:ReinmuthNielsN,
pubmed-author:RensinghoffSonjaS,
pubmed-author:RothGerald JGJ,
pubmed-author:SchwöppeChristianC,
pubmed-author:ThomasMichaelM
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pubmed:issnType |
Print
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pubmed:volume |
31
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
621-6
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pubmed:meshHeading |
pubmed-meshheading:17671690-Automation,
pubmed-meshheading:17671690-Cell Line, Tumor,
pubmed-meshheading:17671690-Cells, Cultured,
pubmed-meshheading:17671690-Endothelium, Vascular,
pubmed-meshheading:17671690-Gene Expression Regulation, Neoplastic,
pubmed-meshheading:17671690-Humans,
pubmed-meshheading:17671690-Indoles,
pubmed-meshheading:17671690-Lung Neoplasms,
pubmed-meshheading:17671690-Platelet-Derived Growth Factor,
pubmed-meshheading:17671690-RNA,
pubmed-meshheading:17671690-Recombinant Proteins,
pubmed-meshheading:17671690-Vascular Endothelial Growth Factor A
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pubmed:year |
2007
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pubmed:articleTitle |
Paracrine interactions of vascular endothelial growth factor and platelet-derived growth factor in endothelial and lung cancer cells.
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pubmed:affiliation |
Department of Internal Medicine-Thoracic Oncology, Clinic for Thoracic Diseases, University of Heidelberg, Heidelberg, Germany. niels.reinmuth@thoraxklinik-heidelberg.de
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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