In situ construction of ligand nano-network to integrin αvβ3 for angiogenesis inhibition

被引:1
|
作者
Ziming Chen [1 ,2 ]
Kuo Zhang [2 ]
Jiaqi Fan [2 ]
Yu Fan [2 ]
Chao Yang [2 ]
Wen Tian [2 ]
Yuan Li [2 ]
Wenliang Li [1 ]
Jingping Zhang [1 ]
Hao Wang [2 ]
Lei Wang [2 ]
机构
[1] Faculty of Chemistry,Northeast Normal University
[2] CAS Center for Excellence in Nanoscience,CAS Key Laboratory for Biomedical Effects of Nanomaterials and Nanosafety,National Center for Nanoscience and Technology (NCNST)
基金
中国国家自然科学基金;
关键词
D O I
暂无
中图分类号
R318.08 [生物材料学]; TB383.1 [];
学科分类号
070205 ; 0805 ; 080501 ; 080502 ; 1406 ;
摘要
Angiogenesis occurs during the process of tumor growth,invasion and metastasis,and is essential for the survival of solid tumors.As an integrin significantly ove rexpressed in human tumor vascular endothelial cells,αvβ3is a suitable targeting site for anti-angiogenesis of tumor.We designed and prepared a selfassembling peptide(SAP) with the ability to targeting αvβ3and self-assembly.SAP formed nanoparticles in solution and transformed into nanofibrous network once specifically binding to integrin αvβ3on the surface of human umbilical vein endothelial cells(HUVECs).The SAP network stably anchored on HUVECs over 24 h,which consequently resulted in high-efficient inhibition of vascularization.In vitro anti-angiogenesis experiment displayed that the inhibition rate of tube-formation reached 94.9%.In vivo anti-angiogenesis array based on chick chorioallantoic membrane(CAM) model exhibited that the SAP had an inhibition rate up to 63.1%.These results indicated the outstanding anti-angiogenic ability of SAP,potentially for tumor therapy.
引用
收藏
页码:3107 / 3112
页数:6
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