| Literature DB >> 12947097 |
Kevin H Mayo1, Ruud P M Dings, Carolee Flader, Irina Nesmelova, Balasz Hargittai, Daisy W J van der Schaft, Loes I van Eijk, Dinesha Walek, Judy Haseman, Thomas R Hoye, Arjan W Griffioen.
Abstract
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.Entities:
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Year: 2003 PMID: 12947097 DOI: 10.1074/jbc.M308608200
Source DB: PubMed Journal: J Biol Chem ISSN: 0021-9258 Impact factor: 5.157