Matrix metalloproteinase-1 and -3 in breast cancer: Correlation with progesterone receptors and other clinicopathologic features

被引:67
作者
Nakopoulou, L
Giannopoulou, I
Gakiopoulou, H
Liapis, H
Tzonou, A
Davaris, PS
机构
[1] Univ Athens, Sch Med, Dept Pathol, GR-11527 Athens, Greece
[2] Univ Athens, Sch Med, Dept Hyg & Epidemiol, GR-10679 Athens, Greece
[3] Washington Univ, Dept Pathol, St Louis, MO 63130 USA
关键词
MMP-1; MMP-3; mRNA; breast cancer; progesterone receptors;
D O I
10.1016/S0046-8177(99)90120-X
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
Although matrix metalloproteinases (MMPs) are implicated in breast cancer progression, the contribution of MMP-1 and MMP-3 to this process, has not been thoroughly investigated. Matrix metalloproteinases (MMPs) are important at several points during multistage neoplastic progression. Immunohistochemistry (Strept-ABC-HRP method) and in situ hybridization were performed to detect MMP-1, MMM-3 proteins, and MMP-3 mRNA, respectively, in 77 infiltrative breast carcinomas. MMP-1, MMP-3 protein, and MMP-3 mRNA detection were analyzed in parallel with clinicopathologic features (menopausal status, histological type, nuclear and histological grade, stage) and the immunohistochemical reactivity of estrogen (ER), progesterone (PR) receptors, and c-erbB-2 oncoprotein in breast carcinomas. Statistical analysis was performed using the multiple linear regression test.. Immunoreactivity for MMP-1 and MMP-3 was observed in 59 of 77 (77%) and 22 of 77 (28.5%) breast carcinomas and was evaluated separately in cancer cells and in stromal fibroblasts. MMP-3 mRNA was detected in 72 of 77 (93.5%) carcinomas exclusively in stromal cells within the tumors or in the marginal portion, of tumors. MMP-1 protein immunoreactivity in stromal fibroblasts but not in cancer cells showed a statistically significant correlation with tumor stage (P = .04). MMP-1 reactivity either in stromal or in cancer cells showed a statistically significant inverse correlation with PR expression (P = .04 and P = .04, respectively). MMP-3 protein immunoreactivity in cancer or stromal cells and MMP-3 mRNA expression was not associated with the clinicopathologic features studied. MMP-3 mRNA was detected more often in ductal carcinomas. These results indicate that MMP-1 may contribute to breast cancer invasiveness. Furthermore, they suggest differential functions for MMP-1 and MMP-3 in breast cancer progression. Copyright (C) 1999 by W.B. Saunders Company.
引用
收藏
页码:436 / 442
页数:7
相关论文
共 45 条
[1]   METALLOPROTEINASE AND TIMP EXPRESSION BY THE HUMAN BREAST-CARCINOMA CELL-LINE 8701-BC [J].
ALESSANDRO, R ;
MINAFRA, S ;
PUCCIMINAFRA, I ;
ONISTO, M ;
GARBISA, S ;
MELCHIORI, A ;
TETLOW, L ;
WOOLLEY, DE .
INTERNATIONAL JOURNAL OF CANCER, 1993, 55 (02) :250-255
[2]  
ARMITAGE P, 1987, STATISTICAL METHODS, P296
[3]  
Bramhall SR, 1997, J PATHOL, V182, P347, DOI 10.1002/(SICI)1096-9896(199707)182:3<347::AID-PATH848>3.0.CO
[4]  
2-J
[5]   TRANSFORMING GROWTH-FACTOR-BETA MEDIATES THE PROGESTERONE SUPPRESSION OF AN EPITHELIAL METALLOPROTEINASE BY ADJACENT STROMA IN THE HUMAN ENDOMETRIUM [J].
BRUNER, KL ;
RODGERS, WH ;
GOLD, LI ;
KORC, M ;
HARGROVE, JT ;
MATRISIAN, LM ;
OSTEEN, KG .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1995, 92 (16) :7362-7366
[6]  
CASE JP, 1990, J IMMUNOL, V145, P3755
[7]   Reduction in Gal-alpha 1,3-Gal epitope expression in transgenic mice expressing human H-transferase [J].
Chen, CG ;
Fisicaro, N ;
Shinkel, TA ;
Aitken, V ;
Katerelos, M ;
vanDenderen, BJW ;
Tange, MJ ;
Crawford, RJ ;
Robins, AJ ;
Pearse, MJ ;
dApice, AJF .
XENOTRANSPLANTATION, 1996, 3 (01) :69-75
[8]  
Chen Wen-Tien, 1992, Current Opinion in Cell Biology, V4, P802
[9]  
CLAVEL C, 1992, B CANCER, V79, P261
[10]  
DIAZMECO MT, 1991, J BIOL CHEM, V266, P22597