MMP inhibitors: experimental and clinical studies

被引:36
作者
Belotti, D [1 ]
Paganoni, P [1 ]
Giavazzi, R [1 ]
机构
[1] Mario Negri Inst Pharmacol Res, Lab Biol & Treatment Metastasis, I-24125 Bergamo, Italy
关键词
metalloproteases; MMP inhibitors; markers;
D O I
10.1177/172460089901400406
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Matrix metalloproteases (MMPs) are a family of structurally related enzymes that are capable of degrading proteins of the extracellular matrix. These enzymes play a role in tissue remodelling associated with both physiological and pathogenic processes. A high expression of MMPs is associated with cancer malignancy: it is related to the tumor's ability to metastasize and to the process of angiogenesis. Treatment with MMP inhibitors alone or in combination with cytotoxic therapy is an interesting novel approach to control tumor progression. The expected mechanism of action of these compounds and the difference in side effects compared to cytotoxic drugs make the definition of endpoints and the assessment of response difficult. Furthermore, it is not yet clear whether tumor vascularization or, more specifically MMP expression/activation should be a criterion of eligibility for this kind of treatment. This review provides an overview of the characteristics of MMPs and their role in tumor progression, metastasis and angiogenesis. Preclinical and clinical studies with synthetic MMP inhibitors are described. The presence of MMPs in biological fluids of patients and their use in prognostic evaluation and in determining the efficacy of treatment with MMP inhibitors is discussed.
引用
收藏
页码:232 / 238
页数:7
相关论文
共 67 条
[41]   CYTOKINE REGULATION OF METALLOPROTEINASE GENE-EXPRESSION [J].
MAUVIEL, A .
JOURNAL OF CELLULAR BIOCHEMISTRY, 1993, 53 (04) :288-295
[42]   MEMBRANE AND MATRIX LOCALIZATION OF PROTEINASES - A COMMON THEME IN TUMOR-CELL INVASION AND ANGIOGENESIS [J].
MOSCATELLI, D ;
RIFKIN, DB .
BIOCHIMICA ET BIOPHYSICA ACTA, 1988, 948 (01) :67-85
[43]  
Moses MA, 1998, CANCER RES, V58, P1395
[44]   Cloning of a disintegrin metalloproteinase that processes precursor tumour-necrosis factor-alpha [J].
Moss, ML ;
Jin, SLC ;
Milla, ME ;
Burkhart, W ;
Carter, HL ;
Chen, WJ ;
Clay, WC ;
Didsbury, JR ;
Hassler, D ;
Hoffman, CR ;
Kost, TA ;
Lambert, MH ;
Leesnitzer, MA ;
McCauley, P ;
McGeehan, G ;
Mitchell, J ;
Moyer, M ;
Pahel, G ;
Rocque, W ;
Overton, LK ;
Schoenen, F ;
Seaton, T ;
Su, JL ;
Warner, J ;
Willard, D ;
Becherer, JD .
NATURE, 1997, 385 (6618) :733-736
[45]   EXPRESSION AND ACTIVITY OF MMPS AND THEIR REGULATORS IN OVARIAN-CANCER [J].
NAYLOR, MS ;
STAMP, GW ;
DAVIES, BD ;
BALKWILL, FR .
INTERNATIONAL JOURNAL OF CANCER, 1994, 58 (01) :50-56
[46]   Active and tissue inhibitor of matrix metalloproteinase-free gelatinase B accumulates within human microvascular endothelial vesicles [J].
Nguyen, M ;
Arkell, J ;
Jackson, CJ .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (09) :5400-5404
[47]   CYTOKINES AND PROTEASES IN INVASIVE PROCESSES - MOLECULAR SIMILARITIES BETWEEN INFLAMMATION AND CANCER [J].
OPDENAKKER, G ;
VANDAMME, J .
CYTOKINE, 1992, 4 (04) :251-258
[48]  
OVERALL CM, 1991, J BIOL CHEM, V266, P14064
[49]  
Page J. G., 1998, Proceedings of the American Association for Cancer Research Annual Meeting, V39, P596
[50]  
PRAGAWOJTOWICZ S, 1998, J CLIN ONCOL, V16, P2150