Hepatocyte growth factor/scatter factor enhances the invasion of mesothelioma cell lines and the expression of matrix metalloproteinases

被引:61
作者
Harvey, P [1 ]
Clark, IM
Jaurand, MC
Warn, RM
Edwards, DR
机构
[1] Univ E Anglia, Sch Biol Sci, Norwich NR4 7TJ, Norfolk, England
[2] Fac Med, INSERM, U139, F-94010 Creteil, France
关键词
HGF/SF; mesothelioma; cell motility; invasion; MMP; TIMP;
D O I
10.1054/bjoc.2000.1445
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Hepatocyte growth factor/scatter factor (HGF/SF) is a multifunctional factor involved both in development and tissue repair, as well as pathological processes such as cancer and metastasis. It has been identified in vivo in many types of tumours together with its tyrosine kinase receptor, Met. We show here that exogenous HGF/SF acts as a strong chemoattractant for human mesothelioma cell lines. The factor also enhanced cell adhesion to and invasion into Matrigel. The mesothelioma cell lines synthesized a panel of matrix metalloproteinases critical for tumour progression such as MMP-1, 2, 3, 9 and membrane-bound MT1-MMP. HGF/SF stimulated the expression of MMP-1, 9 and MT1-MMP and had a slight effect on expression of the MMP inhibitor TIMP-1 but not TIMP-2. However, there was no simple correlation between the levels of MMPs and TIMPs of the cell lines and their different invasion properties or between HGF/SF stimulatory effects on MMP expression and invasion. In addition, effects of protease inhibitors on invasion suggested that serine proteases were also expressed in human mesothelioma cell lines and were involved in HGF/SF-induced invasion. The results show a predominant role for HGF/SF in mesothelioma cell invasion, stimulating simultaneously adhesion, motility, invasion and regulation of MMP and TIMP levels. (C) 2000 Cancer Research Campaign.
引用
收藏
页码:1147 / 1153
页数:7
相关论文
共 54 条
[1]  
ALLAN JA, 1991, J CELL SCI, V99, P789
[2]   Pathology of malignant mesothelioma [J].
Attanoos, RL ;
Gibbs, AR .
HISTOPATHOLOGY, 1997, 30 (05) :403-418
[3]  
Beviglia L, 1999, INT J CANCER, V83, P640, DOI 10.1002/(SICI)1097-0215(19991126)83:5<640::AID-IJC13>3.0.CO
[4]  
2-D
[5]   IDENTIFICATION OF THE HEPATOCYTE GROWTH-FACTOR RECEPTOR AS THE C-MET PROTOONCOGENE PRODUCT [J].
BOTTARO, DP ;
RUBIN, JS ;
FALETTO, DL ;
CHAN, AML ;
KMIECIK, TE ;
VANDEWOUDE, GF ;
AARONSON, SA .
SCIENCE, 1991, 251 (4995) :802-804
[6]   HEPATOCYTE GROWTH-FACTOR IS A POTENT ANGIOGENIC FACTOR WHICH STIMULATES ENDOTHELIAL-CELL MOTILITY AND GROWTH [J].
BUSSOLINO, F ;
DIRENZO, MF ;
ZICHE, M ;
BOCCHIETTO, E ;
OLIVERO, M ;
NALDINI, L ;
GAUDINO, G ;
TAMAGNONE, L ;
COFFER, A ;
COMOGLIO, PM .
JOURNAL OF CELL BIOLOGY, 1992, 119 (03) :629-641
[7]   MONOCLONAL-ANTIBODIES AGAINST HUMAN FIBROBLAST COLLAGENASE AND THE DESIGN OF AN ENZYME-LINKED-IMMUNOSORBENT-ASSAY TO MEASURE TOTAL COLLAGENASE [J].
CLARK, IM ;
POWELL, LK ;
WRIGHT, JK ;
CAWSTON, TE ;
HAZLEMAN, BL .
MATRIX, 1992, 12 (06) :475-480
[8]   Matrix metalloproteinases and the development of cancer [J].
Coussens, LM ;
Werb, Z .
CHEMISTRY & BIOLOGY, 1996, 3 (11) :895-904
[9]   MT1-MMP on the cell surface causes focal degradation of gelatin films [J].
d'Ortho, MP ;
Stanton, H ;
Butler, M ;
Atkinson, SJ ;
Murphy, G ;
Hembry, RM .
FEBS LETTERS, 1998, 421 (02) :159-164
[10]  
DIRENZO MF, 1991, ONCOGENE, V6, P1997