Stromelysin-3 in the Biology of the Normal and Neoplastic Mammary Gland

被引:20
作者
Rio, Marie-Christine [1 ]
Lefebvre, Olivier [1 ]
Santavicca, Maria [1 ]
Noel, Agnes [1 ]
Chenard, Marie-Pierre [2 ]
Anglard, Patrick [1 ]
Byrne, Jennifer A. [1 ]
Okada, Akiko [1 ]
Regnier, Catherine H. [1 ]
Masson, Regis [1 ]
Bellocq, Jean-Pierre [2 ]
Basset, Paul [1 ]
机构
[1] Univ Louis Pasteur, IGBMC, Ctr Natl Rech Sci, Inst Natl Sante & Rech Med,U184, F-67404 Illkirch Graffenstaden, CU De Strasbour, France
[2] CHU Hautepierre, Serv Anat Pathol Gen, F-67098 Strasbourg, France
关键词
Cancer cell invasion/survival; development; metalloproteinases; stromelysin-3; tumorigenicity;
D O I
10.1007/BF02013646
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Stromelysin-3 (ST3)(4) is an extracellular proteinase predominantly expressed in fibroblasts. The particular structural features and in vitro functions of this molecule suggest it could be the first member of a new subgroup of the matrix metalloproteinase family. ST3 is transiently expressed during mammary gland post-weaning involution, embryonic implantation, various organogeneses, and during amphibian metamorphosis. Moreover, ST3 is expressed in a panel of human invasive carcinomas including breast, colon, and head and neck carcinomas. Almost all ST3-expressing tissues show intense extracellular matrix remodeling activities including the loss of basement membrane integrity. Thus, either directly, or indirectly in association with other proteinases, ST3 might be involved in tissue remodeling processes occurring in both physiological and pathological processes. In vitro and in vivo studies using malignant cells stably transfected in such a way as to modulate their ST3 expression levels indicate that ST3 modifies neither cell proliferation nor invasive properties, but rather favors tumor cell survival in host tissues. This hypothesis is consistent with clinical data showing that ST3 expression could be predictive of tumor progression leading to metastases.
引用
收藏
页码:231 / 240
页数:10
相关论文
共 58 条
[1]   STRUCTURE AND PROMOTER CHARACTERIZATION OF THE HUMAN STROMELYSIN-3 GENE [J].
ANGLARD, P ;
MELOT, T ;
GUERIN, E ;
THOMAS, G ;
BASSET, P .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1995, 270 (35) :20337-20344
[2]   A NOVEL METALLOPROTEINASE GENE SPECIFICALLY EXPRESSED IN STROMAL CELLS OF BREAST CARCINOMAS [J].
BASSET, P ;
BELLOCQ, JP ;
WOLF, C ;
STOLL, I ;
HUTIN, P ;
LIMACHER, JM ;
PODHAJCER, OL ;
CHENARD, MP ;
RIO, MC ;
CHAMBON, P .
NATURE, 1990, 348 (6303) :699-704
[3]  
Bellocq J-P., UNPUB
[4]   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
[5]  
Bernstein Lori R., 1994, Current Opinion in Oncology, V6, P106, DOI 10.1097/00001622-199401000-00015
[6]   MOLECULAR ASPECTS OF MESENCHYMAL-EPITHELIAL INTERACTIONS [J].
BIRCHMEIER, C ;
BIRCHMEIER, W .
ANNUAL REVIEW OF CELL BIOLOGY, 1993, 9 :511-540
[7]   PROTEOLYTIC REMODELING OF EXTRACELLULAR-MATRIX [J].
BIRKEDALHANSEN, H .
CURRENT OPINION IN CELL BIOLOGY, 1995, 7 (05) :728-735
[8]   THE TISSUE INHIBITOR OF METALLOPROTEINASES-3 GENE IN BREAST-CARCINOMA - IDENTIFICATION OF MULTIPLE POLYADENYLATION SITES AND A STROMAL PATTERN OF EXPRESSION [J].
BYRNE, JA ;
TOMASETTO, C ;
ROUYER, N ;
BELLOCQ, JP ;
RIO, MC ;
BASSET, P .
MOLECULAR MEDICINE, 1995, 1 (04) :418-427
[9]  
DECLERCK YA, 1992, CANCER RES, V52, P701
[10]  
Docherty A. J. E, 1994, CLIN EXP METASTAS, V12, P25