Antiangiogenic properties of gold nanoparticles

被引:379
作者
Mukherjee, P
Bhattacharya, R
Wang, P
Wang, L
Basu, S
Nagy, JA
Atala, A
Mukhopadhyay, D
Soker, S
机构
[1] Mayo Clin Fdn, Dept Biochem & Mol Biol, Rochester, MN 55905 USA
[2] Mayo Clin Fdn, Dept Biomed Engn, Rochester, MN 55905 USA
[3] Beth Israel Deaconess Med Ctr, Dept Pathol, Boston, MA 02215 USA
[4] Harvard Univ, Sch Med, Boston, MA 02115 USA
[5] Forest Inst Regenerat Med, Winston Salem, NC USA
关键词
D O I
10.1158/1078-0432.CCR-04-2482
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Here, we report an intrinsic property of gold nanoparticles (nanogold): they can interact selectively with heparin-binding glycoproteins and inhibit their activity. Gold nanoparticles specifically bound vascular permeability factor/vascular endothelial growth factor (VPF/VEGF)-165 and basic fibroblast growth factor, two endothelial cell mitogens and mediators of angiogenesis resulting in inhibition of endothelial/fibroblast cell proliferation in vitro and VEGF-induced permeability as well as angiogenesis in vivo. In contrast, nanogold did not inhibit VEGF-121 or epidermal growth factor, two non-heparin-binding growth factors, mediated cell proliferation. Gold nanoparticles significantly inhibited VEGF receptor-2 phosphorylation, intracellular calcium release, and migration and RhoA activation in vitro. These results report for the first time a novel property of gold nanoparticles to bind heparin-binding proteins and thereby inhibit their subsequent signaling events.
引用
收藏
页码:3530 / 3534
页数:5
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