The matrix metalloproteinase-9/neutrophil gelatinase-associated lipocalin complex plays a role in breast tumor growth and is present in the urine of breast cancer patients

被引:234
作者
Fernández, CA
Yan, L
Lous, G
Yang, J
Kutok, JL
Moses, MA
机构
[1] Harvard Univ, Childrens Hosp Boston, Vasc Biol Program, Sch Med, Boston, MA 02115 USA
[2] Harvard Univ, Childrens Hosp Boston, Dept Surg, Sch Med, Boston, MA 02115 USA
[3] Brigham & Womens Hosp, Dept Pathol, Boston, MA 02115 USA
关键词
D O I
10.1158/1078-0432.CCR-04-2391
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose: Having previously shown that the binding of neutrophil gelatinase-associated lipocalin (NGAL) to matrix metalloproteinase-9 (MMP-9) protects this extracellular matrix remodeling enzyme from autodegradation, we hypothesized that the addition of NGAL to breast cancer cells, which do not express this protein but do express MMP-9, might result in a more aggressive phenotype in vivo. Based on our previous reports that MMPs can be detected in the urine of cancer patients, we also asked whether MMP-9/NGAL could be detected in the urine of breast cancer patients and whether it might be predictive of disease status. Experimental Design: Clones of MCF-7 human breast cancer cells differentially expressing NGAL were generated by stable transfection with human NGAL expression constructs. The established clones were then implanted s.c. in immunodeficient mice and tumor growth was monitored. In addition, we analyzed the urine of individuals with breast cancer and age-matched, sex-matched controls using gelatin zymography for the presence of MMP-9/NGAL. Results: Increased NGAL expression resulted in significant stimulation of tumor growth. Immunohistochemical analysis of MCF-7 tumors revealed that the NGAL-overexpressing ones exhibited increased growth rates that were accompanied by increased levels of MMP-9, increased angiogenesis, and an increase in the tumor cell proliferative fraction. In addition, MMP-9/NGAL complex was detected in 86.36% of the urine samples from breast cancer patients but not in those from healthy age and sex-matched controls. Conclusions: These findings suggest, for the first time, that NGAL may play an important role in breast cancer in vivo by protecting MMP-9 from degradation thereby enhancing its enzymatic activity and facilitating angiogenesis and tumor growth. Clinically, these data suggest that the urinary detection of MMP-9/NGAL may be useful in noninvasively predicting disease status of breast cancer patients.
引用
收藏
页码:5390 / 5395
页数:6
相关论文
共 31 条
[1]   Gene expression of angiogenic factors correlates with metastatic potential of prostate cancer cells [J].
Aalinkeel, R ;
Nair, MPN ;
Sufrin, G ;
Mahajan, SA ;
Chadha, KC ;
Chawda, RP ;
Schwartz, SA .
CANCER RESEARCH, 2004, 64 (15) :5311-5321
[2]   STUDIES OF THE RELEASE AND TURNOVER OF A HUMAN NEUTROPHIL LIPOCALIN [J].
AXELSSON, L ;
BERGENFELDT, M ;
OHLSSON, K .
SCANDINAVIAN JOURNAL OF CLINICAL & LABORATORY INVESTIGATION, 1995, 55 (07) :577-588
[3]   CLONING AND EXPRESSION OF HUMAN NEUTROPHIL LIPOCALIN CDNA DERIVED FROM BONE-MARROW AND OVARIAN-CANCER CELLS [J].
BARTSCH, S ;
TSCHESCHE, H .
FEBS LETTERS, 1995, 357 (03) :255-259
[4]   Matrix metalloproteinase-9 triggers the angiogenic switch during carcinogenesis [J].
Bergers, G ;
Brekken, R ;
McMahon, G ;
Vu, TH ;
Itoh, T ;
Tamaki, K ;
Tanzawa, K ;
Thorpe, P ;
Itohara, S ;
Werb, Z ;
Hanahan, D .
NATURE CELL BIOLOGY, 2000, 2 (10) :737-744
[5]  
BRAUNHUT SJ, 1994, J BIOL CHEM, V269, P13472
[6]   Neutrophil gelatinise-associated lipocalin is up-regulated in human epithelial cells by IL-1β, but not by TNF-α [J].
Cowland, JB ;
Sorensen, OE ;
Sehested, M ;
Borregaard, N .
JOURNAL OF IMMUNOLOGY, 2003, 171 (12) :6630-6639
[7]   Matrix metalloproteinase-2 is required for the switch to the angiogenic phenotype in a tumor model [J].
Fang, JM ;
Shing, Y ;
Wiederschain, D ;
Yan, L ;
Butterfield, C ;
Jackson, G ;
Harper, J ;
Tamvakopoulos, G ;
Moses, MA .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2000, 97 (08) :3884-3889
[8]   Structural and functional uncoupling of the enzymatic and angiogenic inhibitory activities of tissue inhibitor of metalloproteinase-2 (TIMP-2) -: Loop 6 is a novel angiogenesis inhibitor [J].
Fernández, CA ;
Butterfield, C ;
Jackson, G ;
Moses, MA .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2003, 278 (42) :40989-40995
[9]   Role of angiogenesis in tumor growth and metastasis [J].
Folkman, J .
SEMINARS IN ONCOLOGY, 2002, 29 (06) :15-18
[10]   Neutrophil gelatinase-associated lipocalin in normal and neoplastic human tissues. Cell type-specific pattern of expression [J].
Friedl, A ;
Stoesz, SP ;
Buckley, P ;
Gould, MN .
HISTOCHEMICAL JOURNAL, 1999, 31 (07) :433-441