Tissue inhibitors of metalloproteases: Regulation and biological activities

被引:120
作者
Fassina, G
Ferrari, N
Brigati, C
Benelli, R
Santi, L
Noonan, DM
Albini, A
机构
[1] Ist Nazl Ric Canc, Ctr Biotecnol Avanzate, Mol Biol Lab, I-16132 Genoa, Italy
[2] CNR, Ctr Neurofisiol Cerebrale, Genoa, Italy
[3] Univ Genoa, Dipartimento Oncol Biol & Genet, Genoa, Italy
[4] Ctr Biotecnol Avanzate, CBA, Genoa, Italy
关键词
basement membrane; invasion; metalloproteases; TIMPs;
D O I
10.1023/A:1006797522521
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
A central role in tissue invasion is played by proteases that degrade extracellular matrices; in particular specific metalloproteases (MMPs) have been frequently correlated with the invasive potential of tumor cells and with the angiogenic process. MMPs are tightly regulated by molecules controlling their activation and by specific inhibitors of MMPs, known as the Tissue Inhibitors of MetalloProteases or TIMPs. Four TIMP family members are currently known. An imbalance between MMPs and TIMPs is linked to the degradation of the extracellular matrix associated with several physiologic and pathologic events including angiogenesis, invasion and metastasis. TIMPs are not only the `guardians' of tissue degradation, they are able to control cell proliferation and cell survival as well. Given the critical role that TIMPs play, it is vital to know how the expression of TIMPs is controlled. Here we review the major biological properties and the molecular regulation of the TIMP expression.
引用
收藏
页码:111 / 120
页数:10
相关论文
共 96 条
[1]  
Ahonen M, 1998, CANCER RES, V58, P2310
[2]   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
[3]   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
[4]   Angiogenesis at the interface between basic and clinical research [J].
Albini, A ;
Noonan, D ;
Santi, L .
INTERNATIONAL JOURNAL OF BIOLOGICAL MARKERS, 1999, 14 (04) :202-206
[5]  
ALBINI A, 1998, PATHOL ONCOL RES, V4, P1
[6]   TARGETED DISRUPTION OF THE TISSUE INHIBITOR OF METALLOPROTEINASES GENE INCREASES THE INVASIVE BEHAVIOR OF PRIMITIVE MESENCHYMAL CELLS DERIVED FROM EMBRYONIC STEM-CELLS INVITRO [J].
ALEXANDER, CM ;
WERB, Z .
JOURNAL OF CELL BIOLOGY, 1992, 118 (03) :727-739
[7]  
Aoudjit F, 1998, J IMMUNOL, V160, P2967
[8]   GENE ENCODING A NOVEL MURINE TISSUE INHIBITOR OF METALLOPROTEINASES (TIMP), TIMP-3, IS EXPRESSED IN DEVELOPING MOUSE EPITHELIA, CARTILAGE, AND MUSCLE, AND IS LOCATED ON MOUSE CHROMOSOME-10 [J].
APTE, SS ;
HAYASHI, K ;
SELDIN, MF ;
MATTEI, MG ;
HAYASHI, M ;
OLSEN, BR .
DEVELOPMENTAL DYNAMICS, 1994, 200 (03) :177-197
[9]   CLONING OF THE CDNA-ENCODING HUMAN TISSUE INHIBITOR OF METALLOPROTEINASES-3 (TIMP-3) AND MAPPING OF THE TIMP3 GENE TO CHROMOSOME-22 [J].
APTE, SS ;
MATTEI, MG ;
OLSEN, BR .
GENOMICS, 1994, 19 (01) :86-90
[10]  
Bachman KE, 1999, CANCER RES, V59, P798