血管内皮生长抑制物
血管生成
血管生成抑制剂
CD30
肿瘤坏死因子α
生物
内皮干细胞
癌症研究
分子生物学
细胞因子
血管内皮生长因子A
血管内皮生长因子
免疫学
体外
生物化学
肿瘤细胞
血管内皮生长因子受体
作者
Yifan Zhai,Jian Ni,Gongwei Jiang,Jiamo Lu,Lily Xing,Clint Lincoln,Kenneth C. Carter,Fouad Janat,DIANE KOZAK,Simin Xu,Lorena Rojas,Bharat Aggarwal,Steve Ruben,Lu‐Yuan Li,Reiner Gentz,Guoliang Yu
标识
DOI:10.1096/fasebj.13.1.181
摘要
A novel member of the tumor necrosis factor (TNF) family has been identified from the human umbilical vein endothelial cell cDNA library, named vascular endothelial growth inhibitor (VEGI). The VEGI gene was mapped to human chromosome 9q32. The cDNA for VEGI encodes a protein of 174 amino acid residues with the characteristics of a type II transmembrane protein. Its amino acid sequence is 20-30% identical to other members of the TNF family. Unlike other members of the TNF family, VEGI is expressed predominantly in endothelial cells. Local production of a secreted form of VEGI via gene transfer caused complete suppression of the growth of MC-38 murine colon cancers in syngeneic C57BL/6 mice. Histological examination showed marked reduction of vascularization in MC-38 tumors that expressed soluble but not membrane-bound VEGI or were transfected with control vector. The conditioned media from soluble VEGI-expressing cells showed marked inhibitory effect on in vitro proliferation of adult bovine aortic endothelial cells. Our data suggest that VEGI is a novel angiogenesis inhibitor of the TNF family and functions in part by directly inhibiting endothelial cell proliferation. The results further suggest that VEGI maybe highly valuable toward angiogenesis-based cancer therapy.
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