Regulation of cell signalling by uPAR

被引:744
|
作者
Smith, Harvey W. [1 ]
Marshall, Chris J. [2 ]
机构
[1] McGill Univ, Goodman Canc Ctr, Montreal, PQ H3A 1A3, Canada
[2] Inst Canc Res, Canc Res UK Ctr Cell & Mol Biol, London SW3 6JB, England
关键词
PLASMINOGEN-ACTIVATOR RECEPTOR; EPIDERMAL-GROWTH-FACTOR; INCREASED CYCLOOXYGENASE-2 EXPRESSION; LIGAND-BINDING DOMAIN; FOCAL ADHESION KINASE; GPI-ANCHORED UPAR; UROKINASE-RECEPTOR; IN-VIVO; BREAST-CANCER; DEFICIENT MICE;
D O I
10.1038/nrm2821
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Urokinase-type plasminogen activator receptor (uPAR) expression is elevated during inflammation and tissue remodelling and in many human cancers, in which it frequently indicates poor prognosis. uPAR regulates proteolysis by binding the extracellular protease urokinase-type plasminogen activator (uPA; also known as urokinase) and also activates many intracellular signalling pathways. Coordination of extracellular matrix (ECM) proteolysis and cell signalling by uPAR underlies its important function in cell migration, proliferation and survival and makes it an attractive therapeutic target in cancer and inflammatory diseases. uPAR lacks transmembrane and intracellular domains and so requires transmembrane co-receptors for signalling. Integrins are essential uPAR signalling co-receptors and a second uPAR ligand, the ECM protein vitronectin, is also crucial for this process.
引用
收藏
页码:23 / 36
页数:14
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