Bastadin 6, a spongean brominated tyrosine derivative, inhibits tumor angiogenesis by inducing selective apoptosis to endothelial cells

被引:41
作者
Aoki, Shunji
Cho, Seok-hwan
Ono, Mayumi
Kuwano, Takashi
Nakao, Shintaro
Kuwano, Michihiko
Nakagawa, Shinsaku
Gao, Jian-Qing
Mayumi, Tadanori
Shibuya, Masabumi
Kobayashi, Motomasa
机构
[1] Osaka Univ, Grad Sch Pharmaceut Sci, Suita, Osaka 5650871, Japan
[2] Kyushu Univ, Grad Sch Med Sci, Dept Med Biochem, Fukuoka 812, Japan
[3] Kurume Univ, Res Ctr Innovat Canc Therapy, 21st Century COE Program Med Sci, Fukuoka, Japan
[4] Univ Tokyo, Inst Med Sci, Dept Genet, Tokyo, Japan
关键词
apoptosis; anti-angiogenesis; anti-tumor activity; bastadin; 6;
D O I
10.1097/00001813-200603000-00005
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Bastadin 6, a macrocyclic tetramer of a brominated tyrosine derivative, was isolated from a marine sponge and its anti-angiogenic activity was evaluated. Bastadin 6 was found to inhibit vascular endothelial growth factor (VEGF)- or basic fibroblast growth factor (bFGF)-dependent proliferation (IC50=0.052 mu mol/l) of human umbilical vein endothelial cells (HUVECs) 20- to 100-fold selectively in comparison with normal fibroblast (3Y1) or several tumor cells (KB3-1, K562 and Neuro2A). Bastadin 6 also inhibited VEGF- or bFGF-induced tubular formation (0.1 mu mol/l, 6 h treatment) and VEGF-induced migration (1 mu mol/l, 4h treatment) of HUVECs. Moreover, bastadin 6 almost completely blocked VEGF- or bFGF-induced in vivo neovascularization in the mice corneal assay and suppressed growth of s.c. inoculated A431 solid tumor in nude mice (100 mg/kg, i.p.). Bastadin 6 induced cell death of HUVECs with an apoptotic phenotype, whereas it showed no effect on the VEGF-induced auto-phosphorylation of VEGF receptors FIt-1 and KDR/FIk-1. These results suggest that the anti-angiogenic effect of bastadin 6 is closely related to selective induction activity of apoptosis against endothelial cells.
引用
收藏
页码:269 / 278
页数:10
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