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Cancer Research 69, 8009, October 15, 2009. Published Online First October 6, 2009;
doi: 10.1158/0008-5472.CAN-08-4889
© 2009 American Association for Cancer Research

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Experimental Therapeutics, Molecular Targets, and Chemical Biology

Inhibition of Tumor Cell Growth, Invasion, and Metastasis by EXEL-2880 (XL880, GSK1363089), a Novel Inhibitor of HGF and VEGF Receptor Tyrosine Kinases

Fawn Qian1, Stefan Engst1, Kyoko Yamaguchi1, Peiwen Yu1, Kwang-Ai Won1, Lillian Mock1, Tracy Lou1, Jenny Tan1, Connie Li1, Danny Tam1, Julie Lougheed1, F. Michael Yakes1, Frauke Bentzien1, Wei Xu1, Tal Zaks2, Richard Wooster2, Joel Greshock2 and Alison H. Joly1

1 Exelixis, Inc., South San Francisco, California and 2 GlaxoSmithKline R&D, Division of Oncology, Collegeville, Pennsylvania

Requests for reprints: Alison H. Joly, Exelixis, Inc., 170 Harbor Way, South San Francisco, CA 94083. Phone: 650-837-7000; Fax: 650-837-8315; E-mail: ajoly{at}exelixis.com.

Key Words: Met • VEGFR • antitumor • antiangiogenesis

The Met receptor tyrosine kinase and its ligand, hepatocyte growth factor (HGF), are overexpressed and/or activated in a wide variety of human malignancies. Vascular endothelial growth factor (VEGF) receptors are expressed on the surface of vascular endothelial cells and cooperate with Met to induce tumor invasion and vascularization. EXEL-2880 (XL880, GSK1363089) is a small-molecule kinase inhibitor that targets members of the HGF and VEGF receptor tyrosine kinase families, with additional inhibitory activity toward KIT, Flt-3, platelet-derived growth factor receptor β, and Tie-2. Binding of EXEL-2880 to Met and VEGF receptor 2 (KDR) is characterized by a very slow off-rate, consistent with X-ray crystallographic data showing that the inhibitor is deeply bound in the Met kinase active site cleft. EXEL-2880 inhibits cellular HGF-induced Met phosphorylation and VEGF-induced extracellular signal-regulated kinase phosphorylation and prevents both HGF-induced responses of tumor cells and HGF/VEGF-induced responses of endothelial cells. In addition, EXEL-2880 prevents anchorage-independent proliferation of tumor cells under both normoxic and hypoxic conditions. In vivo, these effects produce significant dose-dependent inhibition of tumor burden in an experimental model of lung metastasis. Collectively, these data indicate that EXEL-2880 may prevent tumor growth through a direct effect on tumor cell proliferation and by inhibition of invasion and angiogenesis mediated by HGF and VEGF receptors. [Cancer Res 2009;69(20):8009–16]







HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Cancer Research Clinical Cancer Research
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Molecular Cancer Research Cancer Prevention Research
Cancer Prevention Journals Portal Cancer Reviews Online
Annual Meeting Education Book Meeting Abstracts Online
Copyright © 2009 by the American Association for Cancer Research.