UROKINASE AND MACROPHAGES IN TUMOR ANGIOGENESIS

被引:111
作者
HILDENBRAND, R
DILGER, I
HORLIN, A
STUTTE, HJ
机构
[1] Senckenbergisches Zentrum der Pathologie, Klinikum der JW Goethe-Universitay, Frankfurt, 60596
关键词
UROKINASE; MACROPHAGES; ANGIOGENESIS; VASCULAR INVASION; BREAST CANCER;
D O I
10.1038/bjc.1995.419
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Recent studies have shown that elevated levels of urokinase plasminogen activator (uPA) and plasminogen activator inhibitor 1 (PAI-1) in breast cancer correlate with an increased risk of a reduced relapse-free survival time and shortened overall survival times. Urokinase PA and PAI-1 are independent prognostic indicators for breast cancer, The fact that plasminogen activators are indispensable for tube formation of microvascular cells and that they may induce angiogenesis in vitro strongly suggests a role for uPA and PAI-1 in tumour neovascularisation. Because macrophages and tumour cells produce uPA, we postulate a close collaboration between tumour cells and tumour-associated macrophages in angiogenesis. To investigate how uPA levels and macrophage counts in tumour tissue correlate with angiogenesis, we counted microvessels and determined uPA levels and macrophage content in 42 primary invasive breast carcinomas. Using light microscopy, we highlighted the vessels by staining their endothelium cells immunocytochemically for CD31 and factor VIlI and the macrophages for CD68. After obtaining tumour tissue extracts, we determined the uPA and PAI-1 levels by ELISA. A positive correlation between microvessel density, vascular invasion, uPA level, macrophage content and proliferation rate was found.
引用
收藏
页码:818 / 823
页数:6
相关论文
共 35 条
[1]   EXPRESSION AND SECRETION OF TYPE-BETA TRANSFORMING GROWTH-FACTOR BY ACTIVATED HUMAN MACROPHAGES [J].
ASSOIAN, RK ;
FLEURDELYS, BE ;
STEVENSON, HC ;
MILLER, PJ ;
MADTES, DK ;
RAINES, EW ;
ROSS, R ;
SPORN, MB .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1987, 84 (17) :6020-6024
[2]   VASCULAR-PERMEABILITY FACTOR (VASCULAR ENDOTHELIAL GROWTH-FACTOR) GENE IS EXPRESSED DIFFERENTIALLY IN NORMAL-TISSUES, MACROPHAGES, AND TUMORS [J].
BERSE, B ;
BROWN, LF ;
VANDEWATER, L ;
DVORAK, HF ;
SENGER, DR .
MOLECULAR BIOLOGY OF THE CELL, 1992, 3 (02) :211-220
[3]   LEAKY VESSELS, FIBRIN DEPOSITION, AND FIBROSIS - A SEQUENCE OF EVENTS COMMON TO SOLID TUMORS AND TO MANY OTHER TYPES OF DISEASE [J].
BROWN, LF ;
DVORAK, AM ;
DVORAK, HF .
AMERICAN REVIEW OF RESPIRATORY DISEASE, 1989, 140 (04) :1104-1107
[4]   IMMUNOENZYMATIC LABELING OF MONOCLONAL-ANTIBODIES USING IMMUNE-COMPLEXES OF ALKALINE-PHOSPHATASE AND MONOCLONAL ANTI-ALKALINE PHOSPHATASE (APAAP COMPLEXES) [J].
CORDELL, JL ;
FALINI, B ;
ERBER, WN ;
GHOSH, AK ;
ABDULAZIZ, Z ;
MACDONALD, S ;
PULFORD, KAF ;
STEIN, H ;
MASON, DY .
JOURNAL OF HISTOCHEMISTRY & CYTOCHEMISTRY, 1984, 32 (02) :219-229
[5]   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
[6]  
DVORAK HF, 1986, NEW ENGL J MED, V315, P161
[7]  
FALCONE DJ, 1993, J BIOL CHEM, V268, P11951
[8]   TRANSFORMING GROWTH-FACTOR-BETA-1 STIMULATES MACROPHAGE UROKINASE EXPRESSION AND RELEASE OF MATRIX-BOUND BASIC FIBROBLAST GROWTH-FACTOR [J].
FALCONE, DJ ;
MCCAFFREY, TA ;
HAIMOVITZFRIEDMAN, A ;
GARCIA, M .
JOURNAL OF CELLULAR PHYSIOLOGY, 1993, 155 (03) :595-605
[9]  
FOEKENS JA, 1992, CANCER RES, V52, P6101
[10]  
GELEHRTER TD, 1983, MOL CELL BIOCHEM, V53-4, P11