Matrix metalloproteinase inhibitors - an emphasis on gastrointestinal malignancies

被引:21
作者
Chau, I [1 ]
Rigg, A [1 ]
Cunningham, D [1 ]
机构
[1] Royal Marsden Hosp, Dept Med, Gastrointestinal Unit, Sutton SM2 5PT, Surrey, England
关键词
matrix metalloproteinases; matrix metalloproteinase inhibitors; metastasis; angiogenesis; cytostatic agents;
D O I
10.1016/S1040-8428(02)00015-X
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Gastrointestinal malignancies are the commonest sites of human cancer collectively. Improved understanding of tumour biology in the last few decades has allowed the identification of cellular pathways responsible for the autonomous growth and replication in cancer cells. There is considerable preclinical evidence implicating matrix metalloproteinases (MMPs) in cancer dissemination and tumour angiogenesis. Effective MMP inhibitors (MMPIs) may, therefore, hold an important key in the treatment of gastrointestinal cancers. MMPIs are cytostatic agents and traditional values of tumour regression may not be the best measures of treatment efficacy. Biological correlation studies are increasingly being incorporated into the early development of these agents, but many of those studies lack preclinical validation and are often chosen on availability rather than biological plausibility. Disappointing results with many MMPIs that have entered phase III testing so far would prompt for identification of reliable surrogate biomarkers and incorporation of functional imaging in the clinical development of matrix metalloproteinase inhibitors in gastrointestinal malignancies. In this review, the integral part in which MMPs are involved in cancer growth and metastases will be presented. This is then followed by a discussion of the challenges that clinicians are facing in assessing the efficacy of MMPIs and finally a review of the clinical studies of the synthetic MMPIs in development. (C) 2002 Elsevier Science Ireland Ltd. All rights reserved.
引用
收藏
页码:151 / 176
页数:26
相关论文
共 149 条
[1]  
AHMANN FR, 2001, P AN M AM SOC CLIN, V20, pA174
[2]  
Ahonen M, 1998, CANCER RES, V58, P2310
[3]   TUMOR-CELL INVASION INHIBITED BY TIMP-2 [J].
ALBINI, A ;
MELCHIORI, A ;
SANTI, L ;
LIOTTA, LA ;
BROWN, PD ;
STETLERSTEVENSON, WG .
JOURNAL OF THE NATIONAL CANCER INSTITUTE, 1991, 83 (11) :775-779
[4]   ANGIOGENIC POTENTIAL IN-VIVO BY KAPOSIS-SARCOMA CELL-FREE SUPERNATANTS AND HIV-1 TAT PRODUCT - INHIBITION OF KS-LIKE LESIONS BY TISSUE INHIBITOR OF METALLOPROTEINASE-2 [J].
ALBINI, A ;
FONTANINI, G ;
MASIELLO, L ;
TACCHETTI, C ;
BIGINI, D ;
LUZZI, P ;
NOONAN, DM ;
STETLERSTEVENSON, WG .
AIDS, 1994, 8 (09) :1237-1244
[5]   INHIBITION OF COLLAGENOLYTIC ACTIVITY AND METASTASIS OF TUMOR-CELLS BY A RECOMBINANT HUMAN TISSUE INHIBITOR OF METALLOPROTEINASES [J].
ALVAREZ, OA ;
CARMICHAEL, DF ;
DECLERCK, YA .
JOURNAL OF THE NATIONAL CANCER INSTITUTE, 1990, 82 (07) :589-595
[6]  
AnandApte B, 1997, INVEST OPHTH VIS SCI, V38, P817
[7]  
Anderson IC, 1996, CANCER RES, V56, P715
[8]   TUMOR ANGIOGENESIS AS A PROGNOSTIC ASSAY FOR INVASIVE DUCTAL BREAST-CARCINOMA [J].
AXELSSON, K ;
LJUNG, BME ;
MOORE, DH ;
THOR, AD ;
CHEW, KL ;
EDGERTON, SM ;
SMITH, HS ;
MAYALL, BH .
JOURNAL OF THE NATIONAL CANCER INSTITUTE, 1995, 87 (13) :997-1008
[9]   Inhibition of invasion and induction of apoptotic cell death of cancer cell lines by overexpression of TIMP-3 [J].
Baker, AH ;
George, SJ ;
Zaltsman, AB ;
Murphy, G ;
Newby, AC .
BRITISH JOURNAL OF CANCER, 1999, 79 (9-10) :1347-1355
[10]   NOVEL METHODS FOR THE DETERMINATION OF THE ANGIOGENIC ACTIVITY OF HUMAN TUMORS [J].
BARBARESCHI, M ;
GASPARINI, G ;
MORELLI, L ;
FORTI, S ;
DALLAPALMA, P .
BREAST CANCER RESEARCH AND TREATMENT, 1995, 36 (02) :181-192