Isolation of a novel peptide homing to tumor-derived neovasculature that suppresses tumor growth

被引:6
作者
Asai, T
Fukatsu, H
Kuromi, K
Ogino, K
Tanaka, M
Oku, N
Taki, T
机构
[1] Univ Shizuoka, Sch Pharmaceut Sci, Dept Med Biochem, Shizuoka 4228526, Japan
[2] Otsuka Pharmaceut Co Ltd, Inst Mol Sci Med, Tokushima 7710192, Japan
关键词
phage-displayed peptide library; angiogenesis; tumor dormancy; drug delivery system;
D O I
10.1248/bpb.25.904
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Novel peptides homing to angiogenic vessels were recently isolated from a phage-displayed random pentadecapeptide library, and peptides having WRP sequence showed tumor growth suppression. In this study, we observed that another novel sequence, PVVLFPLH, suppressed tumor growth in vivo. Through the study of tumor growth suppression by the 5-mer peptides derived from this sequence, we determined the epitope sequence to be LFPLH. LFPLH, but not the shuffled peptide FHLLP, suppressed the migration of vascular endothelial growth factor-stimulated human umbilical vein endothelial cells. Interestingly, growth suppression of LFPLH against the cells as well as tumor cells was not observed in vitro. Therefore LFPLH may function to induce tumor dormancy through inhibition of angiogenesis.
引用
收藏
页码:904 / 906
页数:3
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