血管生成
HT1080型
生物
细胞外基质
癌症研究
细胞生物学
碱性成纤维细胞生长因子
内皮干细胞
血管生成抑制剂
分子生物学
生长因子
体外
肿瘤细胞
生物化学
受体
作者
Mohanraj Dhanabal,William J. LaRochelle,Michael Jeffers,John L. Herrmann,Luca Rastelli,William F. McDonald,Rajeev A. Chillakuru,Meijia Yang,Ferenc Boldog,Muralidhara Padigaru,Kelly D. McQueeney,Frank Wu,S A Minskoff,Richard A. Shimkets,Henri S. Lichenstein
出处
期刊:PubMed
日期:2002-07-01
卷期号:62 (13): 3834-41
被引量:82
摘要
The angiopoietins comprise a family of proteins that have pro or antiangiogenic activities. Through a proprietary technology designed to identify transcripts of all expressed genes, we isolated a cDNA encoding an angiopoietin-related protein that we designate angioarrestin. The mRNA expression profile of angioarrestin was striking in that it was down-regulated in many tumor tissues when compared with adjacent nontumor tissue, suggesting a role for this protein in tumor inhibition. To test this hypothesis, we ectopically expressed angioarrestin in HT1080 tumor cells and measured pulmonary tumor nodule formation in nude mice. HT1080 cells expressing angioarrestin showed a marked reduction in the number and size of tumor nodules. In vitro, the recombinant protein was systematically tested in a number of endothelial cell assays and found to block critical processes involved in the angiogenic cascade, such as vascular endothelial growth factor/basic fibroblast growth factor-mediated endothelial cell proliferation, migration, tubular network formation, and adhesion to extracellular matrix proteins. These findings reveal a novel function for angioarrestin as an angiogenesis inhibitor and indicate that the molecule may be a potential cancer therapeutic.
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