Maz51, an indolinone that inhibits endothelial cell and tumor cell growth in vitro, suppresses tumor growth in vivo

被引:51
|
作者
Kirkin, V
Thiele, W
Baumann, P
Mazitschek, R
Rohde, K
Fellbrich, G
Weich, H
Waltenberger, J
Giannis, A
Sleeman, JP
机构
[1] Forschungszentrum Karlsruhe, Inst Genet & Toxikol, D-76021 Karlsruhe, Germany
[2] Univ Leipzig, Inst Organ Chem, Leipzig, Germany
[3] Univ Ulm Klinikum, Innere Med Abt 2, Ulm, Germany
[4] German Res Ctr Biotechnol, Dept Gene Regulat & Gene Differentat, Div Mol Biotechnol, Braunschweig, Germany
关键词
indolinone; VEGFR-3; lymphangiogenesis; angiogenesis; inhibitor;
D O I
10.1002/ijc.20509
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
We have recently described MAZ51, an indolinone that blocks the ligand-induced autophosphorylation of VEGFR-3, a receptor tyrosine kinase that plays a central role in the regulation of lymphangiogenesis. Here we show that MAZ51 is able to block the proliferation of VEGFR-3-expressing human endothelial cells and is less potently able to induce their apoptosis. MAZ51 also inhibits the proliferation and induces the apoptosis of a variety of non-VEGFR-3-expressing tumor cell lines. These data suggest that MAZ51 blocks the activity of tyrosine kinases in addition to VEGFR-3. In vivo, MAZ51 significantly inhibits the growth of rat mammary carcinomas. These data establish MAZ51 as a compound with antitumor properties that inhibits tumor growth directly and also indirectly by interfering with tumor-host interactions. (C) 2004 Wiley-Liss, Inc.
引用
收藏
页码:986 / 993
页数:8
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