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Inhibition of endothelial cell functions and of angiogenesis by the metastasis inhibitor NAMI-A

机译:转移抑制剂NAMI-A抑制内皮细胞功能和血管生成

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摘要

NAMI-A is a ruthenium-based compound with selective anti-metastasis activity in experimental models of solid tumours. We studied whether this activity was dependent on anti-angiogenic ability of NAMI-A. We thus investigated its in vitro effects on endothelial cell functions necessary for angiogenesis to develop, as well as its in vivo effects in the chick embryo chorioallantoic membrane model. Endothelial cell proliferation, chemotaxis, and secretion of the matrix-degrading enzyme metalloproteinase-2 were inhibited by NAMI-A in a dose-dependent manner, and without morphologic signs of cell apoptosis or necrosis. Lastly, NAMI-A displayed a dose-dependent in vivo anti-angiogenic activity in the chorioallantoic membrane model. These data suggest that the anti-angiogenic activity of NAMI-A can contribute to its anti-metastatic efficacy in mice bearing malignant solid tumours.
机译:NAMI-A是一种基于钌的化合物,在实体瘤的实验模型中具有选择性的抗转移活性。我们研究了这种活性是否取决于NAMI-A的抗血管生成能力。因此,我们研究了其对血管生成发展所必需的内皮细胞功能的体外作用,以及在鸡胚绒膜尿囊膜模型中的体内作用。 NAMI-A以剂量依赖的方式抑制内皮细胞的增殖,趋化性和基质降解酶金属蛋白酶2的分泌,并且没有细胞凋亡或坏死的形态学迹象。最后,NAMI-A在绒毛膜尿囊膜模型中显示出剂量依赖性的体内抗血管生成活性。这些数据表明,NAMI-A的抗血管生成活性可有助于其在患有恶性实体瘤的小鼠中的抗转移功效。

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