Antibodies neutralizing hepsin protease activity do not impact cell growth but inhibit invasion of prostate and ovarian tumor cells in culture

被引:65
作者
Xuan, JA
Schneider, D
Toy, P
Lin, R
Newton, A
Zhu, Y
Finster, S
Vogel, D
Mintzer, B
Dinter, H
Light, D
Parry, R
Polokoff, M
Whitlow, M
Wu, QY
Parry, G
机构
[1] Berlex Biosci, Dept Canc Res, Richmond, CA 94806 USA
[2] Berlex Biosci, Dept Syst Biol, Richmond, CA 94806 USA
[3] Berlex Biosci, Dept Pharmacol, Richmond, CA 94806 USA
[4] Berlex Biosci, Dept Chem, Richmond, CA 94806 USA
关键词
D O I
10.1158/0008-5472.CAN-05-2983
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Hepsin is a type II transmembrane serine protease that is expressed in normal liver, and tit lower levels in kidney, pancreas, and testis. Several studies have shown that hepsin mRNA is significantly elevated in most prostate tumors, as well as a significant fraction of ovarian and renal cell carcinomas and hepatomas. Although the overexpression of mRNA in these tumors has been extensively documented, there has been conflicting literature on whether hepsin plays a role in tumor cell growth and progression. Early literature implied a role for hepsin in human tumor cell proliferation, whereas recent studies with a transgenic mouse model for prostate cancer support a role for hepsin in tumor progression and metastases. To evaluate this issue further, we have expressed am activatable form of hepsin, and have generated a set of monoclonal antibodies that neutralize enzyme activity. The neutralizing antibodies inhibit hepsin enzymatic activity in biochemical and cell-based assays. Selected neutralizing and nonneutralizing antibodies were used in cell-based assays with tumor cells to evaluate the effect. of antibodies on tumor cell growth and invasion. Neutralizing antibodies failed to inhibit the growth of prostate, ovarian, and hepatoma cell lines in culture. However, potent inhibitory effects of the antibodies were seen on invasion of ovarian and prostate cells in transwell-based invasion assays. These results support a role for hepsin in tumor cell progression but not in primary tumor growth. Consistent with this, immunnhistochemical experiments with a mouse monoclonal antibody reveal progressively increased staining of prostate tumors with advanced disease, and in particular, extensive staining of bone metastatic lesions.
引用
收藏
页码:3611 / 3619
页数:9
相关论文
共 31 条
[21]   HEPSIN, A PUTATIVE CELL-SURFACE SERINE-PROTEASE, IS REQUIRED FOR MAMMALIAN-CELL GROWTH [J].
TORRESROSADO, A ;
OSHEA, KS ;
TSUJI, A ;
CHOU, SH ;
KURACHI, K .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1993, 90 (15) :7181-7185
[22]  
TSUJI A, 1991, J BIOL CHEM, V266, P16948
[23]  
TSUJI A, 1991, BIOMED BIOCHIM ACTA, V50, P791
[24]  
Welsh JB, 2001, CANCER RES, V61, P5974
[25]   Generation and characterization of mice deficient in hepsin, a hepatic transmembrane serine protease [J].
Wu, QY ;
Yu, DY ;
Post, J ;
Halks-Miller, M ;
Sadler, JE ;
Morser, J .
JOURNAL OF CLINICAL INVESTIGATION, 1998, 101 (02) :321-326
[26]   Type II transmembrane serine proteases [J].
Wu, QY .
CELL SURFACE PROTEASES, 2003, 54 :167-206
[27]   Cloning and characterization of the cDNA for human airway trypsin-like protease [J].
Yamaoka, K ;
Masuda, K ;
Ogawa, H ;
Takagi, K ;
Umemoto, N ;
Yasuoka, S .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (19) :11895-11901
[28]   Corin, a mosaic transmembrane serine protease encoded by a novel cDNA from human heart [J].
Yan, W ;
Sheng, N ;
Seto, M ;
Morser, J ;
Wu, QY .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (21) :14926-14935
[29]   Corin, a transmembrane cardiac serine protease, acts as a pro-atrial natriuretic peptide-converting enzyme [J].
Yan, W ;
Wu, FY ;
Morser, J ;
Wu, QY .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2000, 97 (15) :8525-8529
[30]   Mice deficient in hepsin, a serine protease, exhibit normal embryogenesis and unchanged hepatocyte regeneration ability [J].
Yu, IS ;
Chen, HJ ;
Lee, YSE ;
Huang, PH ;
Lin, SR ;
Tsai, TW ;
Lin, SW .
THROMBOSIS AND HAEMOSTASIS, 2000, 84 (05) :865-870