The purpose of this study was to investigate the antitumor activity of SU6668, tyrosine kinase inhibitor of vascular endothelial growth factor receptor 2 (VEGFR2), fibroblast growth factor receptor 1 (FGFR1), and platelet-derived growth factor receptor beta (PDGFRbeta), as single-agent therapy and in combination with paclitaxel on ovarian carcinoma xenograft models transplanted in the peritoneal cavity of nude mice.

The combination of the tyrosine kinase receptor inhibitor SU6668 with paclitaxel affects ascites formation and tumor spread in ovarian carcinoma xenografts growing orthotopically / A. Garofalo, E. Naumova, L. Manenti, C. Ghilardi, G. Ghisleni, M. Caniatti, T. Colombo, J.M. Cherrington, E. Scanziani, M. I. Nicoletti, R. Giavazzi. - In: CLINICAL CANCER RESEARCH. - ISSN 1078-0432. - 9:9(2003 Aug 15), pp. 3476-3485.

The combination of the tyrosine kinase receptor inhibitor SU6668 with paclitaxel affects ascites formation and tumor spread in ovarian carcinoma xenografts growing orthotopically

M. Caniatti;E. Scanziani;
2003

Abstract

The purpose of this study was to investigate the antitumor activity of SU6668, tyrosine kinase inhibitor of vascular endothelial growth factor receptor 2 (VEGFR2), fibroblast growth factor receptor 1 (FGFR1), and platelet-derived growth factor receptor beta (PDGFRbeta), as single-agent therapy and in combination with paclitaxel on ovarian carcinoma xenograft models transplanted in the peritoneal cavity of nude mice.
Animals ; receptor, platelet-derived growth factor beta ; ovarian neoplasms ; vascular endothelial growth factor receptor-2 ; humans ; protein-tyrosine kinases ; enzyme inhibitors ; mice ; mice, nude ; pyrroles ; receptors, fibroblast growth factor ; cell survival ; neoplasm transplantation ; receptor, fibroblast growth factor, type 1 ; receptor protein-tyrosine kinases ; indoles ; paclitaxel ; antineoplastic combined chemotherapy protocols ; time factors ; female
Settore VET/03 - Patologia Generale e Anatomia Patologica Veterinaria
15-ago-2003
http://clincancerres.aacrjournals.org/content/9/9/3476.full
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2434/186589
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