The matrix metalloproteinases and their inhibitors in the treatment of pancreatic cancer

被引:87
作者
Jones, L [1 ]
Ghaneh, P [1 ]
Humphreys, M [1 ]
Neoptolemos, JP [1 ]
机构
[1] Royal Liverpool Univ Hosp, Dept Surg, Liverpool L69 3GA, Merseyside, England
来源
CELL AND MOLECULAR BIOLOGY OF PANCREATIC CARCINOMA: RECENT DEVELOPMENTS IN RESEARCH AND EXPERIMENTAL THERAPY | 1999年 / 880卷
关键词
D O I
10.1111/j.1749-6632.1999.tb09533.x
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Matrix metalloproteinases (MMPs) are a family of zinc-containing proteolytic enzymes that break down extracellular matrix proteins (ECM) in physiological and pathological conditions. Disruption in the tight control of MMP metabolism occurs in cancer, resulting in excessive destruction of the ECM, neovascularization,, tumor spread and metastases. Recent studies-have shown that overexpression of MMPs is associated with poor prognosis, Several MMP inhibitors have been developed and preclinical trials have confirmed a reduction in tumor spread and metastases, Marimastat is a broad spectrum inhibitor, and recent;published results shows the drug is well tolerated in patients with advanced cancer. Phase II studies which have used marimistat alone or in combination, with other cytotoxic agents, have produced encouraging results with improved survival, Phase III trials are now underway for the use of marimastat in advanced pancreatic cancer and as an adjuvant therapy in patients following resection of pancreatic cancer.
引用
收藏
页码:288 / 307
页数:20
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共 133 条
  • [121] URIA JA, 1994, CANCER RES, V54, P2091
  • [122] Inhibition of tumor growth and metastasis of human breast cancer cells transfected with tissue inhibitor of metalloproteinase 4
    Wang, MS
    Liu, YLE
    Greene, J
    Sheng, SJ
    Fuchs, A
    Rosen, EM
    Shi, YE
    [J]. ONCOGENE, 1997, 14 (23) : 2767 - 2774
  • [123] WANG X, 1994, CANCER RES, V54, P4726
  • [124] IMMUNOHISTOCHEMICAL STUDY OF HEPARAN-SULFATE PROTEOGLYCAN IN ADENOCARCINOMAS OF THE PANCREAS
    WANG, ZH
    MANABE, T
    OHSHIO, G
    IMAMURA, T
    YOSHIMURA, T
    SUWA, H
    ISHIGAMI, S
    KYOGOKU, T
    [J]. PANCREAS, 1994, 9 (06) : 758 - 763
  • [125] HUMAN-SKIN FIBROBLAST STROMELYSIN - STRUCTURE, GLYCOSYLATION, SUBSTRATE-SPECIFICITY, AND DIFFERENTIAL EXPRESSION IN NORMAL AND TUMORIGENIC CELLS
    WILHELM, SM
    COLLIER, IE
    KRONBERGER, A
    EISEN, AZ
    MARMER, BL
    GRANT, GA
    BAUER, EA
    GOLDBERG, GI
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1987, 84 (19) : 6725 - 6729
  • [126] CDNA SEQUENCE AND MESSENGER-RNA TISSUE DISTRIBUTION OF A NOVEL HUMAN MATRIX METALLOPROTEINASE WITH A POTENTIAL TRANSMEMBRANE SEGMENT
    WILL, H
    HINZMANN, B
    [J]. EUROPEAN JOURNAL OF BIOCHEMISTRY, 1995, 231 (03): : 602 - 608
  • [127] The soluble catalytic domain of membrane type 1 matrix metalloproteinase cleaves the propeptide of progelatinase A and initiates autoproteolytic activation - Regulation by TIMP-2 and TIMP-3
    Will, H
    Atkinson, SJ
    Butler, GS
    Smith, B
    Murphy, G
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 1996, 271 (29) : 17119 - 17123
  • [128] STRUCTURE-FUNCTION-RELATIONSHIPS IN THE TISSUE INHIBITORS OF METALLOPROTEINASES
    WILLENBROCK, F
    MURPHY, G
    [J]. AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 1994, 150 (06) : S165 - S170
  • [129] Matrilysin: An epithelial matrix metalloproteinase with potentially novel functions
    Wilson, CL
    Matrisian, LM
    [J]. INTERNATIONAL JOURNAL OF BIOCHEMISTRY & CELL BIOLOGY, 1996, 28 (02) : 123 - 136
  • [130] BREAST-CANCER ASSOCIATED STROMELYSIN-3 GENE IS EXPRESSED IN BASAL-CELL CARCINOMA AND DURING CUTANEOUS WOUND-HEALING
    WOLF, C
    CHENARD, MP
    DEGROSSOUVRE, PD
    BELLOCQ, JP
    CHAMBON, P
    BASSET, P
    [J]. JOURNAL OF INVESTIGATIVE DERMATOLOGY, 1992, 99 (06) : 870 - 872