Regulation of cancer invasion and vascularization by plasminogen activator inhibitor-1

被引:16
作者
Noël, A
Bajou, K
Masson, V
Devy, L
Frankenne, F
Rakic, JM
Lambert, V
Carmeliet, P
Foidart, JM
机构
[1] Univ Liege, Lab Tumor & Dev Biol, B-4000 Liege, Belgium
[2] CHU, Dept Ophthalmol, Liege, Belgium
[3] Katholieke Univ Leuven VIB, Ctr Transgene Technol & Gene Therapy, Louvain, Belgium
来源
FIBRINOLYSIS & PROTEOLYSIS | 1999年 / 13卷 / 06期
关键词
D O I
10.1054/fipr.2000.0043
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
Acquisition of invasive/metastaticpotential through protease expression is a key event in tumor progression. The proteolytic enzyme plasmin is generated from the precursor plasminogen by the action of urokinase-type plasminogen activator (urokinase, uPA) or tissue-type plasminogen activator (tPA). Plasminogen activator inhibitor-1 or PAI-1 is the main inhibitor of uPA and tPA. High levels of components of this proteolytic system, including UPA and its cell surface receptor (uPAR), have been correlated with a poor prognosis for different cancers. It was therefore anticipated that PAI-1 expression would be associated with favorable outcome. Paradoxically, high rather than low PAI-1 levels predict poor survival of patients suffering from a variety of cancers. Recent observations indicate a much more complex role of PAI-1 in tumor progression and angiogenesis than initially expected. The exact mechanisms of this multifunctional molecule remain puzzling. (C) 1999 Harcourt Publishers Ltd.
引用
收藏
页码:220 / 225
页数:6
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