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E7080, a multi-targeted tyrosine kinase inhibitor suppresses tumor cell migration and invasion
BACKGROUND: E7080 is an orally active multi-targeted kinase inhibitor whose targets include vascular endothelial growth factor receptors (VEGFR), fibroblast growth factor receptor (FGFR) and platelet derived growth factor receptors (PDGFR). It has been shown to inhibit tumor angiogenesis by targetin...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3154179/ https://www.ncbi.nlm.nih.gov/pubmed/21781317 http://dx.doi.org/10.1186/1471-2407-11-309 |
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author | Glen, Hilary Mason, Susan Patel, Hitesh Macleod, Kenneth Brunton, Valerie G |
author_facet | Glen, Hilary Mason, Susan Patel, Hitesh Macleod, Kenneth Brunton, Valerie G |
author_sort | Glen, Hilary |
collection | PubMed |
description | BACKGROUND: E7080 is an orally active multi-targeted kinase inhibitor whose targets include vascular endothelial growth factor receptors (VEGFR), fibroblast growth factor receptor (FGFR) and platelet derived growth factor receptors (PDGFR). It has been shown to inhibit tumor angiogenesis by targeting endothelial cells. A number of the targets of E7080 are also expressed on tumor cells and here we have looked at the direct effects of E7080 on tumor cell behavior. METHODS: Using a panel of human tumor cell lines we determined the effect of E7080 on cell proliferation, migration and invasion. Inhibition of FGFR and PDGFR signaling in the cells was measured. RESULTS: E7080 had little effect on tumor cell proliferation. However, it blocked migration and invasion at concentrations that inhibited FGFR and PDGFR signaling. Knock-down of PDGFR-β in U2OS osteosarcoma cells also inhibited cell migration which, could not be further inhibited in the presence of E7080. Furthermore, E7080 could not inhibit the migration of a PDGFR negative cell line. CONCLUSION: E7080 does not significantly affect tumor cell proliferation but can inhibit their migration and invasion at concentrations that both inhibit its known targets and are achievable clinically. |
format | Online Article Text |
id | pubmed-3154179 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-31541792011-08-11 E7080, a multi-targeted tyrosine kinase inhibitor suppresses tumor cell migration and invasion Glen, Hilary Mason, Susan Patel, Hitesh Macleod, Kenneth Brunton, Valerie G BMC Cancer Research Article BACKGROUND: E7080 is an orally active multi-targeted kinase inhibitor whose targets include vascular endothelial growth factor receptors (VEGFR), fibroblast growth factor receptor (FGFR) and platelet derived growth factor receptors (PDGFR). It has been shown to inhibit tumor angiogenesis by targeting endothelial cells. A number of the targets of E7080 are also expressed on tumor cells and here we have looked at the direct effects of E7080 on tumor cell behavior. METHODS: Using a panel of human tumor cell lines we determined the effect of E7080 on cell proliferation, migration and invasion. Inhibition of FGFR and PDGFR signaling in the cells was measured. RESULTS: E7080 had little effect on tumor cell proliferation. However, it blocked migration and invasion at concentrations that inhibited FGFR and PDGFR signaling. Knock-down of PDGFR-β in U2OS osteosarcoma cells also inhibited cell migration which, could not be further inhibited in the presence of E7080. Furthermore, E7080 could not inhibit the migration of a PDGFR negative cell line. CONCLUSION: E7080 does not significantly affect tumor cell proliferation but can inhibit their migration and invasion at concentrations that both inhibit its known targets and are achievable clinically. BioMed Central 2011-07-22 /pmc/articles/PMC3154179/ /pubmed/21781317 http://dx.doi.org/10.1186/1471-2407-11-309 Text en Copyright ©2011 Glen et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Glen, Hilary Mason, Susan Patel, Hitesh Macleod, Kenneth Brunton, Valerie G E7080, a multi-targeted tyrosine kinase inhibitor suppresses tumor cell migration and invasion |
title | E7080, a multi-targeted tyrosine kinase inhibitor suppresses tumor cell migration and invasion |
title_full | E7080, a multi-targeted tyrosine kinase inhibitor suppresses tumor cell migration and invasion |
title_fullStr | E7080, a multi-targeted tyrosine kinase inhibitor suppresses tumor cell migration and invasion |
title_full_unstemmed | E7080, a multi-targeted tyrosine kinase inhibitor suppresses tumor cell migration and invasion |
title_short | E7080, a multi-targeted tyrosine kinase inhibitor suppresses tumor cell migration and invasion |
title_sort | e7080, a multi-targeted tyrosine kinase inhibitor suppresses tumor cell migration and invasion |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3154179/ https://www.ncbi.nlm.nih.gov/pubmed/21781317 http://dx.doi.org/10.1186/1471-2407-11-309 |
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