Suppr超能文献

一种新型去整合素沙尔莫辛可抑制肿瘤血管生成。

A novel disintegrin salmosin inhibits tumor angiogenesis.

作者信息

Kang I C, Lee Y D, Kim D S

机构信息

Department of Biochemistry, College of Science, and Bioproducts Research Center, Yonsei University, Seoul, Korea.

出版信息

Cancer Res. 1999 Aug 1;59(15):3754-60.

Abstract

Salmosin is a snake venom-derived novel disintegrin that antagonizes platelet aggregation. In this study, we investigated its functional specificity in tumor angiogenesis. Salmosin significantly inhibited bovine capillary endothelial cell proliferation induced by basic fibroblast growth factor but had no effect on normal growth of the cell. The basic fibroblast growth factor-induced in vivo angiogenesis in the chorioallantoic membrane was disrupted by salmosin treatment without affecting normal embryonic angiogenesis. Adhesion of the bovine capillary endothelial cells to vitronectin was also inhibited by the binding of salmosin to the alpha(v)beta3 integrin. Both the metastatic-tumor growth and the solid-tumor growth that developed in mice were effectively suppressed by salmosin treatment. Several lines of experimental evidence strongly suggest that the tumor-specific antiangiogenic activity of salmosin disrupts tumor growth by blocking the alpha(v)beta3 integrin that is expressed on the vascular endothelial cell surface.

摘要

沙尔莫辛是一种源自蛇毒的新型去整合素,可拮抗血小板聚集。在本研究中,我们研究了其在肿瘤血管生成中的功能特异性。沙尔莫辛显著抑制碱性成纤维细胞生长因子诱导的牛毛细血管内皮细胞增殖,但对细胞的正常生长没有影响。沙尔莫辛处理可破坏碱性成纤维细胞生长因子诱导的尿囊绒膜体内血管生成,而不影响正常胚胎血管生成。沙尔莫辛与α(v)β3整合素结合也抑制了牛毛细血管内皮细胞与玻连蛋白的黏附。沙尔莫辛处理有效抑制了小鼠体内转移性肿瘤生长和实体瘤生长。多项实验证据有力地表明,沙尔莫辛的肿瘤特异性抗血管生成活性通过阻断血管内皮细胞表面表达的α(v)β3整合素来破坏肿瘤生长。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验