ROLE OF MATRIX METALLOPROTEINASES IN INVASION AND METASTASIS - BIOLOGY, DIAGNOSIS AND INHIBITORS

被引:17
作者
MCDONNELL, S
FINGLETON, B
机构
[1] School of Biological Sciences, Dublin City University
关键词
INVASION; METALLOPROTEINASES; METASTASIS; TIMPS;
D O I
10.1007/BF00744674
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
The processes of tumour invasion and subsequent metastasis are the most lethal aspects of cancer. Whilst many factors are involved, the matrix metalloproteinases (MMPs) have been implicated as key-rate limiting enzymes in the invasive process. This family consisting of eight members of similar structure, can be roughly divided into three groups based on substrate specificity. All are secreted in a latent form and require proteolytic cleavage for activation. The expression of these enzymes is regulated at the transcriptional level by a variety of growth factors and oncogenes. They are also regulated at the protein level by a family of specific inhibitors called the tissue inhibitors of metalloproteinases (TIMPs). Studies in human tumour samples have shown a positive correlation between metalloproteinase expression and metastatic potential. The levels of metalloproteinase expression have been manipulated using molecular biology techniques in several cell lines and shown a similar correlation. These results suggest that an understanding of metalloproteinase expression and proteolytic activity may lead to the development of effective therapeutic agents with the potential to reduce the incidence of metastatic cancer.
引用
收藏
页码:367 / 384
页数:18
相关论文
共 110 条
[11]  
CAMPBELL CE, 1991, J BIOL CHEM, V266, P7199
[12]   PRIMARY STRUCTURE AND CDNA CLONING OF HUMAN FIBROBLAST COLLAGENASE INHIBITOR [J].
CARMICHAEL, DF ;
SOMMER, A ;
THOMPSON, RC ;
ANDERSON, DC ;
SMITH, CG ;
WELGUS, HG ;
STRICKLIN, GP .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1986, 83 (08) :2407-2411
[13]   SYSTEMIC ADMINISTRATION OF TIMP IN THE TREATMENT OF COLLAGEN-INDUCED ARTHRITIS IN MICE [J].
CARMICHAEL, DF ;
STRICKLIN, GP ;
STUART, JM .
AGENTS AND ACTIONS, 1989, 27 (3-4) :378-379
[14]   PURIFICATION OF RABBIT BONE INHIBITOR OF COLLAGENASE [J].
CAWSTON, TE ;
GALLOWAY, WA ;
MERCER, E ;
MURPHY, G ;
REYNOLDS, JJ .
BIOCHEMICAL JOURNAL, 1981, 195 (01) :159-165
[15]   FRAGMENTS OF HUMAN FIBROBLAST COLLAGENASE - PURIFICATION AND CHARACTERIZATION [J].
CLARK, IM ;
CAWSTON, TE .
BIOCHEMICAL JOURNAL, 1989, 263 (01) :201-206
[16]   ASSOCIATION OF NM23-H1 ALLELIC DELETIONS WITH DISTANT METASTASES IN COLORECTAL-CARCINOMA [J].
COHN, KH ;
WANG, FS ;
DESOTOLAPAIX, F ;
SOLOMON, WB ;
PATTERSON, LG ;
ARNOLD, MR ;
WEIMAR, J ;
FELDMAN, JG ;
LEVY, AT ;
LEONE, A ;
STEEG, PS .
LANCET, 1991, 338 (8769) :722-724
[17]  
COLLIER IE, 1988, J BIOL CHEM, V263, P6579
[18]   PLASMINOGEN ACTIVATORS, TISSUE DEGRADATION, AND CANCER [J].
DANO, K ;
ANDREASEN, PA ;
GRONDAHLHANSEN, J ;
KRISTENSEN, P ;
NIELSEN, LS ;
SKRIVER, L .
ADVANCES IN CANCER RESEARCH, 1985, 44 :139-266
[19]  
DECLERCK YA, 1991, J BIOL CHEM, V266, P3893
[20]  
DECLERCK YA, 1991, CANCER RES, V51, P2151