Cathepsin B and tumor proteolysis: contribution of the tumor microenvironment

被引:141
作者
Sloane, BF [1 ]
Yan, SQ
Podgorski, I
Linebaugh, BE
Cher, ML
Mai, JX
Cavallo-Medved, D
Sameni, M
Dosescu, J
Moin, K
机构
[1] Wayne State Univ, Dept Pharmacol, Detroit, MI 48201 USA
[2] Wayne State Univ, Barbara Ann Karmanos Canc Inst, Detroit, MI 48201 USA
[3] Wayne State Univ, Dept Urol, Detroit, MI 48201 USA
[4] Wayne State Univ, Sch Med, Dept Pathol, Detroit, MI 48201 USA
关键词
cysteine proteases; stromal elements; inflammatory cells; bone; endothelial cells;
D O I
10.1016/j.semcancer.2004.08.001
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Tumor-stromal interactions induce expression of matrix metalloproteinases and serine proteases and, as shown recently, the cysteine protease cathepsin B. We speculate that such interactions upregulate the transcription factor Ets1, resulting in increased cathepsin B expression. This would be consistent with the observed concomitant upregulation of matrix metalloproteinases and serine proteases as well its with the ability of extracellular matrices and their binding partners to alter cathepsin B expression and secretion. Using a confocal assay to analyze the contribution of tumor-stromal interactions to proteolysis, we have been able to confirm enhanced degradation of extracellular matrices by all three classes of proteases. (C) 2004 Elsevier Ltd. All rights reserved.
引用
收藏
页码:149 / 157
页数:9
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