Inhibitory effect of full-length human endostatin on in vitro angiogenesis

被引:95
作者
Taddei, L
Chiarugi, P
Brogelli, L
Cirri, P
Magnelli, L
Raugei, G
Ziche, M
Granger, HJ
Chiarugi, V
Ramponi, G
机构
[1] Dept Biochem Sci, I-50134 Florence, Italy
[2] Inst Gen Pathol, I-50134 Florence, Italy
[3] Dept Clin & Preclin Pharmacol, I-50134 Florence, Italy
[4] Texas A&M Univ, Hlth Sci Ctr, Cardiovasc Res Inst, College Stn, TX USA
[5] Texas A&M Univ, Hlth Sci Ctr, Dept Med Physiol, College Stn, TX USA
关键词
D O I
10.1006/bbrc.1999.1342
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Endostatin, a C-terminal product of collagen XVIII, is a very powerful angiogenesis inhibitor. In vivo experiments in mice indicate that endostatin dramatically reduces tumor mass without causing the onset of any resistance to the treatment. Recently, a 12-aa shorter human endostatin has been purified from plasma, but is ineffective in in vitro angiogenesis assays. Here we report that the full-length human recombinant endostatin has a potent inhibitory activity in in vitro angiogenesis assays. Two powerful angiogenic factors were used to stimulate endothelial cells: FGF-2 and VEGF-165. Endostatin prevented cell growth both in the basal condition and after stimulation with FGF-2 or VEGF-165. Migration of microvascular endothelial cells toward FGF-2 or VEGF-165 was impaired, both when cells mere pretreated with the inhibitor and when endostatin was added together with the growth factors. Furthermore, experiments of inhibition of proliferation performed on nonmicroendothelial cells showed that endostatin was ineffective. This study indicates that human endostatin is a potent angiogenesis inhibitor and suggests its use in human anticancer therapy. (C) 1999 Academic Press.
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页码:340 / 345
页数:6
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