Expression of cysteine protease inhibitors in human gliomas and meningiomas

被引:22
作者
Sivaparvathi, M
McCutcheon, I
Sawaya, R
Nicolson, GL
Rao, JS
机构
[1] UNIV TEXAS,MD ANDERSON CANCER CTR,DEPT NEUROSURG,HOUSTON,TX 77030
[2] UNIV TEXAS,MD ANDERSON CANCER CTR,DEPT TUMOR BIOL,HOUSTON,TX 77030
关键词
cathepsins; cysteine protease inhibitors; glioblastoma; meningiomas; plasminogen activators;
D O I
10.1007/BF00123393
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Increased levels of human cysteine proteases have been implicated in the progression of tumors from the premalignant to the malignant state, The physiological activities of these proteases are regulated by their interactions,vith specific inhibitors. To our knowledge there have been no previous reports about the cysteine protease inhibitors (CPIs) in human brain tumors. In the study reported here, we determined CPI activity during glioma progression and compared that with normal human brain tissue. We also determined CPI activities in meningioma and glioblastoma cell lines in vitro. This activity was significantly higher in normal brain tissue and low-grade glioma than in anaplastic astrocytoma and glioblastoma. CPI activity was significantly higher in benign and atypical meningioma cell extracts in comparison with those from malignant meningiomas and with those from glioblastoma cell lines. After several passages, one benign meningioma cell line showed reduced levels of CPI and increased levels of cathepsin. Our results suggest that decreases in the activities of CPI may contribute to the malignant properties of brain tumors.
引用
收藏
页码:344 / 350
页数:7
相关论文
共 35 条
[1]   HUMAN CYSTATIN-C - ROLE OF THE N-TERMINAL SEGMENT IN THE INHIBITION OF HUMAN CYSTEINE PROTEINASES AND IN ITS INACTIVATION BY LEUKOCYTE ELASTASE [J].
ABRAHAMSON, M ;
MASON, RW ;
HANSSON, H ;
BUTTLE, DJ ;
GRUBB, A ;
OHLSSON, K .
BIOCHEMICAL JOURNAL, 1991, 273 :621-626
[2]  
ABRAHAMSON M, 1986, J BIOL CHEM, V261, P1282
[3]   HUMAN-KIDNEY CATHEPSIN-B AND CATHEPSIN-L - CHARACTERIZATION AND POTENTIAL ROLE IN DEGRADATION OF GLOMERULAR BASEMENT-MEMBRANE [J].
BARICOS, WH ;
ZHOU, YW ;
MASON, RW ;
BARRETT, AJ .
BIOCHEMICAL JOURNAL, 1988, 252 (01) :301-304
[4]   THE CYSTATINS - A NEW CLASS OF PEPTIDASE INHIBITORS [J].
BARRETT, AJ .
TRENDS IN BIOCHEMICAL SCIENCES, 1987, 12 (05) :193-196
[5]   THE PLACE OF HUMAN GAMMA-TRACE (CYSTATIN-C) AMONGST THE CYSTEINE PROTEINASE-INHIBITORS [J].
BARRETT, AJ ;
DAVIES, ME ;
GRUBB, A .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1984, 120 (02) :631-636
[6]  
BARRETT AJ, 1981, METHOD ENZYMOL, V80, P535
[7]  
BRADFORD MM, 1976, ANAL BIOCHEM, V72, P248, DOI 10.1016/0003-2697(76)90527-3
[8]   INCREASED EXPRESSION OF CATHEPSIN-L AND CATHEPSIN-B AND DECREASED ACTIVITY OF THEIR INHIBITORS IN METASTATIC, RAS-TRANSFORMED NIH-3T3 CELLS [J].
CHAMBERS, AF ;
COLELLA, R ;
DENHARDT, DT ;
WILSON, SM .
MOLECULAR CARCINOGENESIS, 1992, 5 (03) :238-245
[9]  
CHAUHAN SS, 1991, CANCER RES, V51, P1478
[10]  
DENHARDT DT, 1987, ONCOGENE, V2, P55