Overview of matrix metalloproteinase expression in cultured human cells

被引:228
作者
Giambernardi, TA
Grant, GM
Taylor, GP
Hay, RJ
Maher, VM
McCormick, JJ
Klebe, RJ
机构
[1] Univ Texas, Hlth Sci Ctr, Dept Cellular & Struct Biol, San Antonio, TX 78284 USA
[2] American Type Culture Collect, Rockville, MD USA
[3] Michigan State Univ, Ctr Canc, Dept Microbiol, Carcinogenesis Lab, E Lansing, MI 48824 USA
[4] Michigan State Univ, Ctr Canc, Dept Biochem, Carcinogenesis Lab, E Lansing, MI 48824 USA
关键词
collagenases; gelatinases; matrix metalloproteinases; oncogenes; stromelysins;
D O I
10.1016/S0945-053X(98)90019-1
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
The matrix metalloproteinases (MMP) have been implicated in tumor invasion and metastasis both by immunohistochemical studies and from the observation that specific metalloproteinase inhibitors block tumor invasion and metastasis. Oligonucleotide primers for thirteen MMPs (MMP-1, MMP-2, MMP-3, MMP-7, MMP-8, MMP-9, MMP-10, MMP-11, MMP-12, MMP-13, MMP-14, MMP-15, MMP-16) were optimized for use in RT-PCR. A semi-quantitative RT-PCR assay was used to determine the pattern of MMP mRNA expression in 84 normal and transformed or carcinogen transformed human cell lines and strains derived from different tissues. The results demonstrate one or more cell lines which express thirteen members of the MMP family. In addition, various oncogene transfected human fibroblast cell strains were analyzed for MMP expression. We confirm that over-expression of the H-ras oncoprotein correlates with up-regulation of MMP-9 and demonstrate that over-expression of v-sis also up-regulates MMP-9. A cell line immortalized following myc expression was found to up-regulate MMP-7, MMP-11 and MMP-13. Inappropriate expression of several MMP mRNAs was detected in breast, prostate, bone, colon and oral tumor derived cell lines. Identification of at least one cell line expressing each of thirteen MMPs and the observation of oncogene induced expression of several MMPs should facilitate analysis of the transcriptional mechanisms controlling each MMP.
引用
收藏
页码:483 / 496
页数:14
相关论文
共 92 条
[1]   EXPRESSION OF 72-KDA TYPE-IV COLLAGENASE AND INVASION ACTIVITY OF HUMAN GLIOMA-CELLS [J].
ABE, T ;
MORI, T ;
KOHNO, K ;
SEIKI, M ;
HAYAKAWA, T ;
WELGUS, HG ;
HORI, S ;
KUWANO, M .
CLINICAL & EXPERIMENTAL METASTASIS, 1994, 12 (04) :296-304
[2]   ASSOCIATION OF MMP-2 ACTIVATION POTENTIAL WITH METASTATIC PROGRESSION IN HUMAN BREAST-CANCER CELL-LINES INDEPENDENT OF MMP-2 PRODUCTION [J].
AZZAM, HS ;
ARAND, G ;
LIPPMAN, ME ;
THOMPSON, EW .
JOURNAL OF THE NATIONAL CANCER INSTITUTE, 1993, 85 (21) :1758-1764
[3]  
BASSET P, 1994, CANCER-AM CANCER SOC, V74, P1045, DOI 10.1002/1097-0142(19940801)74:3+<1045::AID-CNCR2820741511>3.0.CO
[4]  
2-7
[5]   HUMAN MACROPHAGE METALLOELASTASE - GENOMIC ORGANIZATION, CHROMOSOMAL LOCATION, GENE LINKAGE, AND TISSUE-SPECIFIC EXPRESSION [J].
BELAAOUAJ, A ;
SHIPLEY, JM ;
KOBAYASHI, DK ;
ZIMONJIC, DB ;
POPESCU, N ;
SILVERMAN, GA ;
SHAPIRO, SD .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1995, 270 (24) :14568-14575
[6]   DIRECT EVIDENCE LINKING EXPRESSION OF MATRIX METALLOPROTEINASE-9 (92-KDA GELATINASE/COLLAGENASE) TO THE METASTATIC PHENOTYPE IN TRANSFORMED RAT EMBRYO CELLS [J].
BERNHARD, EJ ;
GRUBER, SB ;
MUSCHEL, RJ .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1994, 91 (10) :4293-4297
[7]   PROTEOLYTIC REMODELING OF EXTRACELLULAR-MATRIX [J].
BIRKEDALHANSEN, H .
CURRENT OPINION IN CELL BIOLOGY, 1995, 7 (05) :728-735
[8]   SOME PRACTICAL CONSIDERATIONS AND APPLICATIONS OF THE NATIONAL-CANCER-INSTITUTE IN-VITRO ANTICANCER DRUG DISCOVERY SCREEN [J].
BOYD, MR ;
PAULI, KD .
DRUG DEVELOPMENT RESEARCH, 1995, 34 (02) :91-109
[9]  
BUTTICE G, 1994, CONTRIB NEPHROL, V107, P101
[10]  
BUTTICE G, 1993, J BIOL CHEM, V268, P7196