Design of a partial peptide mimetic of anginex with antiangiogenic and anticancer activity

被引:57
作者
Mayo, KH
Dings, RPM
Flader, C
Nesmelova, I
Hargittai, B
van der Schaft, DWJ
van Eijk, LI
Walek, D
Haseman, J
Hoye, TR
Griffioen, AW
机构
[1] Univ Minnesota, Hlth Sci Ctr, Dept Biochem, Minneapolis, MN 55455 USA
[2] Univ Minnesota, Dept Mol Biol & Biophys, Minneapolis, MN 55455 USA
[3] Univ Minnesota, Dept Chem, Minneapolis, MN 55455 USA
[4] Univ Hosp Maastricht, Dept Pathol, Res Inst Growth & Dev, Angiogenesis Lab, NL-6202 AZ Maastricht, Netherlands
[5] Univ Hosp Maastricht, Dept Internal Med, Res Inst Growth & Dev, Angiogenesis Lab, NL-6202 AZ Maastricht, Netherlands
关键词
D O I
10.1074/jbc.M308608200
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Based on structure-activity relationships of the angiostatic beta-sheet-forming peptide anginex, we have designed a mimetic, 6DBF7, which inhibits angiogenesis and tumor growth in mice. 6DBF7 is composed of a beta-sheet-inducing dibenzofuran (DBF)-turn mimetic and two short key amino acid sequences from anginex. This novel antiangiogenic molecule is more effective in vivo than parent anginex. In a mouse xenograft model for ovarian carcinoma, 6DBF7 is observed to reduce tumor growth by up to 80%. It is suggested that the activity is based on antiangiogenesis, because in vitro tube formation is inhibited, and because treatment of tumor-bearing mice led to a significant reduction in microvessel density within the tumor. This partial peptide mimetic is the first endothelial cell-specific molecule designed as a substitute for an angiostatic inhibitory peptide.
引用
收藏
页码:45746 / 45752
页数:7
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