Matrix-degrading proteases and angiogenesis during development and tumor formation

被引:129
作者
Werb, Z
Vu, TH
Rinkenberger, JL
Coussens, LM
机构
[1] Univ Calif San Francisco, Dept Anat, San Francisco, CA 94143 USA
[2] Univ Calif San Francisco, Dept Med, San Francisco, CA 94143 USA
[3] Univ Calif San Francisco, Hormone Res Inst, San Francisco, CA 94143 USA
关键词
matrix metalloproteinases; angiogenesis; trophoblast; bone; hypertrophic cartilage; implantation; squamous cell carcinoma; skin; Ets-2; MMP-9; apoptosis; VEG;
D O I
10.1111/j.1699-0463.1999.tb01521.x
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Embryonic development and tumor progression both require the exquisite coordination of programs for extracellular matrix (ECM) formation and remodeling, and those for angiogenesis and vascular development. Without a vascular supply the normal tissue or tumor is limited in size and organization. Without ECM remodeling the alteration of tissue and tumor boundaries and cellular migrations are limited. Recent insights into the molecular mechanisms regulating the extracellular environment of the growing embryonic tissue or tumors have implicated proteases, the matrix metalloproteinases (MMPs) in particular, in both the process of ECM remodeling and angiogenesis, and in a potential causal relationship between these processes. This review focuses on the roles that MMPs play in regulating three processes in which both proteolysis and vascular development are tightly coordinated: embryo implantation, bone development and tumor progression.
引用
收藏
页码:11 / 18
页数:8
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