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
  • [31] Cloning, expression analysis, and structural characterization of seven novel human ADAMTSs, a family of metalloproteinases with disintegrin and thrombospondin-1 domains
    Cal, S
    Obaya, AJ
    Llamazares, M
    Garabaya, C
    Quesada, V
    López-Otín, C
    [J]. GENE, 2002, 283 (1-2) : 49 - 62
  • [32] Matrix metalloproteinase inhibitor COL-3 in the treatment of AIDS-related Kaposi's sarcoma: A phase I AIDS malignancy consortium study
    Cianfrocca, M
    Cooley, TP
    Lee, JY
    Rudek, MA
    Scadden, DT
    Ratner, L
    Pluda, JM
    Figg, WD
    Krown, SE
    Dezube, BJ
    [J]. JOURNAL OF CLINICAL ONCOLOGY, 2002, 20 (01) : 153 - 159
  • [33] Cornelius LA, 1998, J IMMUNOL, V161, P6845
  • [34] Cancer therapy - Matrix metalloproteinase inhibitors and cancer: Trials and tribulations
    Coussens, LM
    Fingleton, B
    Matrisian, LM
    [J]. SCIENCE, 2002, 295 (5564) : 2387 - 2392
  • [35] The PEA3 subfamily of Ets transcription factors synergizes with β-catenin-LEF-1 to activate matrilysin transcription in intestinal tumors
    Crawford, HC
    Fingleton, B
    Gustavson, MD
    Kurpios, N
    Wagenaar, RA
    Hassell, JA
    Matrisian, LM
    [J]. MOLECULAR AND CELLULAR BIOLOGY, 2001, 21 (04) : 1370 - 1383
  • [36] MT1-MMP initiates activation of pro-MMP-2 and integrin αvβ3 promotes maturation of MMP-2 in breast carcinoma cells
    Deryugina, EI
    Ratnikov, B
    Monosov, E
    Postnova, TI
    DiScipio, R
    Smith, JW
    Strongin, AY
    [J]. EXPERIMENTAL CELL RESEARCH, 2001, 263 (02) : 209 - 223
  • [37] cDNA cloning of the murine Pex gene implicated in X-linked hypophosphatemia and evidence for expression in bone
    Du, L
    Desbarats, M
    Viel, J
    Glorieux, FH
    Cawthorn, C
    Ecarot, B
    [J]. GENOMICS, 1996, 36 (01) : 22 - 28
  • [38] Duivenvoorden WCM, 2002, CANCER RES, V62, P1588
  • [39] New functions for the matrix metalloproteinases in cancer progression
    Egeblad, M
    Werb, Z
    [J]. NATURE REVIEWS CANCER, 2002, 2 (03) : 161 - 174
  • [40] Neovastat, a naturally occurring multifunctional antiangiogenic drug, in phase III clinical trials
    Falardeau, P
    Champagne, P
    Poyet, P
    Hariton, C
    Dupont, É
    [J]. SEMINARS IN ONCOLOGY, 2001, 28 (06) : 620 - 625