Bellahcène A, Chaplet M, Bonjean K, Castronovo V
Metastasis Research Laboratory, Center of Experimental Cancer Research, University of Liège, 4000 Liège, Belgium.
Endothelium. 2007 Mar-Apr;14(2):123-30. doi: 10.1080/10623320701347187.
Zoledronate exhibits antiangiogenic properties in vitro and in vivo. Integrins alphavbeta3 and alphavbeta5 are involved in angiogenesis. Because zoledronate inhibits endothelial cell adhesion, the authors explored the hypothesis that it could alter these integrins recruitment to focal adhesion sites. Human umbilical vein endothelial cells (HUVECs) were treated with zoledronate or with mevalonate pathway intermediates geranylgeraniol (GGOH) and farnesol (FOH). Zoledronate generated a significant decrease in alphavbeta3 and alphavbeta5 expression at HUVEC cell surface using flow cytometry and immunofluorescence. This inhibition was reversed by GGOH but not by FOH. Cells cotreated with zoledronate and GGOH were able to attach to vitronectin through alphavbeta3 and alphavbeta5, as confirmed by the use of specific function-blocking antibodies. The authors showed that zoledronate alters endothelial cell integrin-mediated adhesion. This effect is likely to contribute to the previously demonstrated antiangiogenic effect of zoledronate. Whether this mechanism of action also applies to metastatic tumor cells is under investigation.
唑来膦酸在体外和体内均表现出抗血管生成特性。整合素αvβ3和αvβ5参与血管生成。由于唑来膦酸抑制内皮细胞黏附,作者探讨了其是否能改变这些整合素向黏着斑位点募集的假说。用人脐静脉内皮细胞(HUVECs)分别用唑来膦酸或甲羟戊酸途径中间体香叶基香叶醇(GGOH)和法尼醇(FOH)处理。通过流式细胞术和免疫荧光法检测,唑来膦酸使HUVEC细胞表面的αvβ3和αvβ5表达显著降低。这种抑制作用可被GGOH逆转,但不能被FOH逆转。使用特异性功能阻断抗体证实,用唑来膦酸和GGOH共同处理的细胞能够通过αvβ3和αvβ5黏附于玻连蛋白。作者表明,唑来膦酸改变内皮细胞整合素介导的黏附。这种效应可能有助于唑来膦酸先前已证实的抗血管生成作用。这种作用机制是否也适用于转移性肿瘤细胞正在研究中。