Strategies for MMP inhibition in cancer:: Innovations for the post-trial era

被引:1078
作者
Overall, CM
López-Otín, C
机构
[1] Univ Oviedo, Fac Med, Inst Oncol, Dept Bioquim & Biol Mol, E-33006 Oviedo, Spain
[2] Univ British Columbia, Dept Oral Biol & Med Sci, Vancouver, BC V6T 1Z3, Canada
[3] Univ British Columbia, Dept Biochem & Mol Biol, CIHR Grp Matrix Dynam, Vancouver, BC V6T 1Z3, Canada
基金
加拿大健康研究院;
关键词
D O I
10.1038/nrc884
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
For more than two decades, the view that tumour-associated matrix metalloproteinases; (MMPs) were required for peritumour tissue degradation and metastasis dominated the drive to develop MMP inhibitors as anticancer therapeutics. Until recently, clinical trials with MMIP inhibitors have yielded disappointing results, highlighting the need for better insight into the mechanisms by which this growing family of multifunctional enzymes contribute to tumour growth. It is now recognized that MMP activity is tightly regulated at several levels, providing new avenues for blocking these enzymes. What are the different approaches that can be used to target MMPs, and which of these might lead to new therapeutic strategies for cancer?.
引用
收藏
页码:657 / 672
页数:16
相关论文
共 153 条
  • [11] Furin inhibition results in absent or decreased invasiveness and tumorigenicity of human cancer cells
    Bassi, DE
    De Cicco, RL
    Mahloogi, H
    Zucker, S
    Thomas, G
    Klein-Szanto, AJP
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2001, 98 (18) : 10326 - 10331
  • [12] STROMELYSIN-1 - 3-DIMENSIONAL STRUCTURE OF THE INHIBITED CATALYTIC DOMAIN AND OF THE C-TRUNCATED PROENZYME
    BECKER, JW
    MARCY, AI
    ROKOSZ, LL
    AXEL, MG
    BURBAUM, JJ
    FITZGERALD, PMD
    CAMERON, PM
    ESSER, CK
    HAGMANN, WK
    HERMES, JD
    SPRINGER, JP
    [J]. PROTEIN SCIENCE, 1995, 4 (10) : 1966 - 1976
  • [13] Thrombospondin type 1 repeats interact with matrix metalloproteinase 2 - Regulation of metalloproteinase activity
    Bein, K
    Simons, M
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (41) : 32167 - 32173
  • [14] Bello L, 2001, CANCER RES, V61, P8730
  • [15] A novel negative regulatory element in the human collagenase-3 proximal promoter region
    Benderdour, M
    Tardif, G
    Pelletier, JP
    Dupuis, M
    Geng, C
    Martel-Pelletier, J
    [J]. BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2002, 291 (05) : 1151 - 1159
  • [16] Design, synthesis, and characterization of potent, slow-binding inhibitors that are selective for gelatinases
    Bernardo, MM
    Brown, S
    Li, ZH
    Fridman, R
    Mobashery, S
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 2002, 277 (13) : 11201 - 11207
  • [17] Bigg HF, 2001, CANCER RES, V61, P3610
  • [18] Biondi ML, 2000, CLIN CHEM, V46, P2023
  • [19] Putting tumours in context
    Bissell, MJ
    Radisky, D
    [J]. NATURE REVIEWS CANCER, 2001, 1 (01) : 46 - 54
  • [20] Functional and biochemical characterization of ADAMs and their predicted role in protein ectodomain shedding
    Blobel, CP
    [J]. INFLAMMATION RESEARCH, 2002, 51 (02) : 83 - 84