Matrix metalloproteinases and oral cancer

被引:139
作者
Thomas, GT
Lewis, MP
Speight, PM
机构
[1] Univ London, Eastman Dent Inst Oral Healthcare Sci, Dept Oral Pathol, London WC1X 8LD, England
[2] Univ London, Eastman Dent Inst Oral Healthcare Sci, Dept Orthodont, London WC1X 8LD, England
基金
英国医学研究理事会;
关键词
mouth; squamous cell carcinoma; oral cancer; matrix metalloproteinases; MMPs;
D O I
10.1016/S1368-8375(99)00004-4
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
For tumours to invade and metastasise, neoplastic cells must be capable of degrading the extracellular matrix (ECM), and accessing blood vessels and lymphatics. This process is mediated in the pericellular environment and is a highly controlled cascade of events utilising the same mechanisms that normal cells use for migrating through tissue barriers, for example, in development and wound healing. Proteolytic enzymes from several families, including matrix metalloproteinases (MMPs), are involved in ECM remodelling. Increased production of these enzymes has been associated with the invasive and/or metastatic phenotype in many tumours. Several MMPs have been shown to play a role in the invasion and metastasis of oral carcinoma, and it is increasingly apparent that tumour cells, as well as producing endogenous MMP, are capable of utilising MMP produced by tumour stromal cells, indicating an active role for stroma in tumour invasion. It is not clear whether a particular invasive system is favoured by oral carcinoma, but it is likely that further understanding of the interactions between carcinoma and stromal cells will provide an opportunity to refine the therapeutic interventions that are currently being tested. (C) 1999 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:227 / 233
页数:7
相关论文
共 54 条
[1]   Human collagenase-3 is expressed in malignant squamous epithelium of the skin [J].
Airola, K ;
Johansson, N ;
Kariniemi, AL ;
Kahari, VM ;
SaarialhoKere, UK .
JOURNAL OF INVESTIGATIVE DERMATOLOGY, 1997, 109 (02) :225-231
[2]   GENE ENCODING A NOVEL MURINE TISSUE INHIBITOR OF METALLOPROTEINASES (TIMP), TIMP-3, IS EXPRESSED IN DEVELOPING MOUSE EPITHELIA, CARTILAGE, AND MUSCLE, AND IS LOCATED ON MOUSE CHROMOSOME-10 [J].
APTE, SS ;
HAYASHI, K ;
SELDIN, MF ;
MATTEI, MG ;
HAYASHI, M ;
OLSEN, BR .
DEVELOPMENTAL DYNAMICS, 1994, 200 (03) :177-197
[3]   CLONING OF THE CDNA-ENCODING HUMAN TISSUE INHIBITOR OF METALLOPROTEINASES-3 (TIMP-3) AND MAPPING OF THE TIMP3 GENE TO CHROMOSOME-22 [J].
APTE, SS ;
MATTEI, MG ;
OLSEN, BR .
GENOMICS, 1994, 19 (01) :86-90
[4]   Focalized proteolysis: Spatial and temporal regulation of extracellular matrix degradation at the cell surface [J].
Basbaum, CB ;
Werb, Z .
CURRENT OPINION IN CELL BIOLOGY, 1996, 8 (05) :731-738
[5]   Specific, high affinity binding of tissue inhibitor of metalloproteinases-4 (TIMP4) to the COOH-terminal hemopexin-like domain of human gelatinase A - TIMP-4 binds progelatinase A and the COOH-terminal domain in a similar manner to TIMP-2 [J].
Bigg, HF ;
Shi, YE ;
Liu, YLE ;
Steffensen, B ;
Overall, CM .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1997, 272 (24) :15496-15500
[6]   MATRIX METALLOPROTEINASES - A REVIEW [J].
BIRKEDALHANSEN, H ;
MOORE, WGI ;
BODDEN, MK ;
WINDSOR, LJ ;
BIRKEDALHANSEN, B ;
DECARLO, A ;
ENGLER, JA .
CRITICAL REVIEWS IN ORAL BIOLOGY & MEDICINE, 1993, 4 (02) :197-250
[7]   PROTEOLYTIC REMODELING OF EXTRACELLULAR-MATRIX [J].
BIRKEDALHANSEN, H .
CURRENT OPINION IN CELL BIOLOGY, 1995, 7 (05) :728-735
[8]   Cartilage fibronectin isoforms: In search of functions for a special population of matrix glycoproteins [J].
BurtonWurster, N ;
Lust, G ;
MacLeod, JN .
MATRIX BIOLOGY, 1997, 15 (07) :441-454
[9]   Expression of matrix metalloproteinases and tissue inhibitor of metalloproteinases in head and neck squamous cell carcinoma [J].
Charous, SJ ;
Stricklin, GP ;
Nanney, LB ;
Netterville, JL ;
Burkey, BB .
ANNALS OF OTOLOGY RHINOLOGY AND LARYNGOLOGY, 1997, 106 (04) :271-278
[10]   Membrane-type matrix metalloproteinases 1 and 2 exhibit broad-spectrum proteolytic capacities comparable to many matrix metalloproteinases [J].
d'Ortho, MP ;
Will, H ;
Atkinson, S ;
Butler, G ;
Messent, A ;
Gavrilovic, J ;
Smith, B ;
Timpl, R ;
Zardi, L ;
Murphy, G .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 1997, 250 (03) :751-757