Matrix metalloproteinases and their inhibitors in tumour growth and invasion

被引:346
作者
Kähäri, VM
Saarialho-Kere, U
机构
[1] Univ Turku, MediCity Res Lab, FIN-20520 Turku, Finland
[2] Turku Univ, Cent Hosp, Dept Dermatol, Turku, Finland
[3] Univ Turku, Dept Med Biochem, Turku, Finland
[4] Univ Helsinki, Cent Hosp, Dept Dermatol, FIN-00170 Helsinki, Finland
关键词
cancer; invasion; matrix metalloproteinase;
D O I
10.3109/07853899909019260
中图分类号
R5 [内科学];
学科分类号
1002 [临床医学]; 100201 [内科学];
摘要
Controlled degradation of the extracellular matrix (ECM) is crucial for the growth, invasive capacity, metastasis and angiogenesis of tumours. Matrix metalloproteinases (MMPs), a family of zinc-dependent neutral endopeptidases that are collectively capable of degrading essentially all ECM components, apparently play an important role in all of these aspects of tumour development. In addition, there is recent evidence that MMPs are also important for tumour cell survival. at present, therapeutic intervention on tumour growth and invasion based on the inhibition of MMP activity is under intensive investigation, and several MMP inhibitors are already being used on malignant tumours of various organs in clinical trials. In this review we discuss the role of MMPs and their inhibitors in tumour invasion asa basis for prognostic purposes and for targeted therapeutic intervention in cancer.
引用
收藏
页码:34 / 45
页数:12
相关论文
共 137 条
[1]
Ahonen M, 1998, CANCER RES, V58, P2310
[2]
MATRIX METALLOPROTEINASE-2 IS AN INTERSTITIAL COLLAGENASE - INHIBITOR-FREE ENZYME CATALYZES THE CLEAVAGE OF COLLAGEN FIBRILS AND SOLUBLE NATIVE TYPE-I COLLAGEN GENERATING THE SPECIFIC 3/4-LENGTH AND 1/4-LENGTH FRAGMENTS [J].
AIMES, RT ;
QUIGLEY, JP .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1995, 270 (11) :5872-5876
[3]
Expression of collagenases-1 and -3 and their inhibitors TIMP-1 and -3 correlates with the level of invasion in malignant melanomas [J].
Airola, K ;
Karonen, T ;
Vaalamo, M ;
Lehti, K ;
Lohi, J ;
Kariniemi, AL ;
Keski-Oja, J ;
Saarialho-Kere, UK .
BRITISH JOURNAL OF CANCER, 1999, 80 (5-6) :733-743
[4]
Human TIMP-3 is expressed during fetal development, hair growth cycle, and cancer progression [J].
Airola, K ;
Ahonen, M ;
Johansson, N ;
Heikkilä, P ;
Kere, J ;
Kähäri, VM ;
Saarialho-Kere, UK .
JOURNAL OF HISTOCHEMISTRY & CYTOCHEMISTRY, 1998, 46 (04) :437-447
[5]
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
[6]
TNF-α converting enzyme (TACE) is inhibited by TIMP-3 [J].
Amour, A ;
Slocombe, PM ;
Webster, A ;
Butler, M ;
Knight, CG ;
Smith, BJ ;
Stephens, PE ;
Shelley, C ;
Hutton, M ;
Knäuper, V ;
Docherty, AJP ;
Murphy, G .
FEBS LETTERS, 1998, 435 (01) :39-44
[7]
AnandApte B, 1997, INVEST OPHTH VIS SCI, V38, P817
[8]
BAKER AH, IN PRESS BR J CANC
[9]
Matrix metalloproteinases as stromal effectors of human carcinoma progression: Therapeutic implications [J].
Basset, P ;
Okada, A ;
Chenard, MP ;
Kannan, R ;
Stoll, I ;
Anglard, P ;
Bellocq, JP ;
Rio, MC .
MATRIX BIOLOGY, 1997, 15 (8-9) :535-541
[10]
Suppression of in vivo tumor growth and induction of suspension cell death by tissue inhibitor of metalloproteinases (TIMP)-3 [J].
Bian, JH ;
Wang, YL ;
Smith, MR ;
Kim, H ;
Jacobs, C ;
Jackman, J ;
Kung, HF ;
Colburn, NH ;
Sun, Y .
CARCINOGENESIS, 1996, 17 (09) :1805-1811