DTD, an anti-inflammatory ditriazine, inhibits angiogenesis in vitro and in vivo

被引:2
|
作者
Martinez-Poveda, Beatriz [1 ]
Munoz-Chapuli, Ramon [2 ]
Riguera, Ricardo [3 ]
Fernandez, Antonio [4 ]
Medina, Miguel Angel [1 ]
Quesada, Ana R. [1 ]
机构
[1] Univ Malaga, Fac Ciencias, Dept Biol Mol & Bioquim, E-29071 Malaga, Spain
[2] Univ Malaga, Fac Ciencias, Dept Biol Anim, E-29071 Malaga, Spain
[3] Univ Santiago, Dept Quim Organ, Santiago De Compostela, Spain
[4] Edificio CEI, Inst Biomar SA Polig Ind, Leon, Spain
关键词
angiogenesis inhibitor; DTD; ditriazines; endothelial cells;
D O I
10.1111/j.1582-4934.2008.00147.x
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The ditriazine derivative DTD (4,10-dichloropyrido[5,6:4,5]thieno[3,2-d':3,2-d]-1,2,3-ditriazine) has been previously reported to reduce the degree of granulomatous inflammation and vascular density in a murine air pouch granuloma model. The aim of this study was to test whether DTD affects angiogenesis. Our results show that DTD inhibits in vivo angiogenesis in the chorioallantoic membrane (CAM) assay at doses equal or lower than 0.3 nmol/egg. Different in vitro assays were used to study the potential effects of this compound on key steps of angiogenesis, namely, a colorimetric assay of cell proliferation/viability, a morphogenesis on Matrigel assay, zymographic assays for gelatinases and nuclear morphology and cell cycle analysis for apoptosis induction. Our data indicate that DTD inhibits proliferation but does not induce apoptosis in endothelial cells in vitro. DTD suppresses the endothelial capillary-like chord formation at concentrations lower than those required to inhibit proliferation. DTD treatment inhibits the matrix metalloproteinase-2 production in endothelial and fibrosarcoma cells, but does not affect the cyclooxygenase-2 expression in endothelial cells, as assessed by western blot analysis. Taken together, results here presented indicate that DTD exhibits an anti-angiogenic activity that is independent of inflammatory processes and make it a promising drug for further evaluation in the treatment of angiogenesis-related pathologies.
引用
收藏
页码:1211 / 1219
页数:9
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