Emerging concepts in the regulation of membrane-type 1 matrix metalloproteinase activity

被引:46
作者
Gingras, Denis [1 ]
Beliveau, Richard [1 ]
机构
[1] Univ Quebec, Mol Med Lab, Montreal, PQ H3C 3P8, Canada
来源
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR CELL RESEARCH | 2010年 / 1803卷 / 01期
基金
加拿大健康研究院;
关键词
MT1-MMP; Cytoplasmic domain; Signal transduction; ENDOTHELIAL GROWTH-FACTOR; 1-MATRIX METALLOPROTEINASE; CELL-MIGRATION; TYROSINE PHOSPHORYLATION; CYTOPLASMIC TAIL; UP-REGULATION; TUMOR-GROWTH; MTI-MMP; PLASMA-MEMBRANE; MT1-MMP;
D O I
10.1016/j.bbamcr.2009.04.011
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
Pericellular proteolysis mediated by membrane-type 1 matrix metalloproteinase (MT1-MMP) represents an essential component of the cellular machinery involved in the dissolution and penetration of ECM barriers by tumor cells. Although most studies on the proinvasive properties of MT1-MMP have focused on its unusually broad proteolytic activity towards several ECM components and cell surface receptors, recent evidence indicate that the cytoplasmic domain of the enzyme also actively participates in tumor cell invasion by regulating the cell surface localization of MT1-MMP as well as the activation of signal transduction cascades. The identification of the molecular events by which the intracellular domain of MT1-MMP links proteolysis of the surrounding matrix by the enzyme to modification of cell function may thus provide important new information on the mechanisms by which this enzyme controls the invasive behavior of neoplastic cells in vivo. (C) 2009 Elsevier B.V. All rights reserved.
引用
收藏
页码:142 / 150
页数:9
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