Type IV collagen-derived angiogenesis inhibitors

被引:137
作者
Mundel, Thomas M.
Kalluri, Raghu
机构
[1] Harvard Univ, Beth Israel Deaconess Med Ctr, Sch Med, Div Matrix Biol,Dept Med, Boston, MA 02215 USA
[2] Harvard Univ, Sch Med, Dept Biol Chem & Mol Pharmacol, Boston, MA 02215 USA
[3] Harvard MIT Div Hlth Sci & Technol, Boston, MA 02215 USA
关键词
ECM; angiogenesis inhibitor; type IV collagen NC1; tumor;
D O I
10.1016/j.mvr.2007.05.005
中图分类号
R6 [外科学];
学科分类号
1002 ; 100210 ;
摘要
The concept of anti-angiogenesis therapy was introduced by Judah Folkman in 1971 and since then, a plethora of pro- and anti-angiogenic factors have been identified. In the recent years, it has become clear that angiogenesis, the formation of new capillaries from a pre-existing capillary network, is highly regulated by the action of pro- and anti-angiogenic factors. In the healthy adult organism the "angiogenic-switch" is likely turned "Off", i.e. anti-angiogenic factors are likely counteracting the pro-angiogenic factors resulting in a non-angiogenic state. Angiogenesis is encountered during wound healing processes, the female menstrual cycle and endometrial remodeling, as well as during embryonic development and organ growth. In the pathological setting, angiogenesis plays an important role in different diseases like rheumatoid arthritis, psoriasis, macular degeneration, diabetic retinopathy, and tumor growth. In this regard, recent studies have described several endogenous inhibitors of angiogenesis, with a subset derived from extracellular matrix (ECM) proteins. This review will particularly focus on the type IV collagen-derived angiogenesis inhibitors Arresten, Canstatin and Tumstatin. (C) 2007 Elsevier Inc. All rights reserved.
引用
收藏
页码:85 / 89
页数:5
相关论文
共 60 条
[1]   Endothelial progenitor cells for vascular regeneration [J].
Asahara, T ;
Isner, JM .
JOURNAL OF HEMATOTHERAPY & STEM CELL RESEARCH, 2002, 11 (02) :171-178
[2]  
Augustin HG, 2003, OPHTHALMOLOGE, V100, P104, DOI 10.1007/s00347-003-0785-3
[3]   INTEGRIN ALPHA(V)BETA(3) ANTAGONISTS PROMOTE TUMOR-REGRESSION BY INDUCING APOPTOSIS OF ANGIOGENIC BLOOD-VESSELS [J].
BROOKS, PC ;
MONTGOMERY, AMP ;
ROSENFELD, M ;
REISFELD, RA ;
HU, TH ;
KLIER, G ;
CHERESH, DA .
CELL, 1994, 79 (07) :1157-1164
[4]   Angiogenesis in cancer and other diseases [J].
Carmeliet, P ;
Jain, RK .
NATURE, 2000, 407 (6801) :249-257
[5]   Angiogenesis in health and disease [J].
Carmeliet, P .
NATURE MEDICINE, 2003, 9 (06) :653-660
[6]  
Colorado PC, 2000, CANCER RES, V60, P2520
[7]  
FOLKMAN J, 1971, NEW ENGL J MED, V285, P1182
[8]  
FOLKMAN J, 1992, J BIOL CHEM, V267, P10931
[9]   ANGIOGENESIS IN CANCER, VASCULAR, RHEUMATOID AND OTHER DISEASE [J].
FOLKMAN, J .
NATURE MEDICINE, 1995, 1 (01) :27-31
[10]  
FOLKMAN J, 2006, SCI STKE, pPE35