Cathepsin B as a cancer target

被引:316
作者
Gondi, Christopher S. [1 ]
Rao, Jasti S. [1 ,2 ]
机构
[1] Univ Illinois, Coll Med Peoria, Dept Canc Biol & Pharmacol & Neurosurg, Peoria, IL USA
[2] Univ Illinois, Coll Med Peoria, Dept Neurosurg, Peoria, IL USA
关键词
cancer target; cancer therapy; cathepsin B; Cathepsin B signaling; ECM; HUMAN GLIOBLASTOMA CELLS; UROKINASE PLASMINOGEN-ACTIVATOR; MMP-9; GENE-EXPRESSION; CYSTATIN-A STEFIN; TUMOR-GROWTH; CYSTEINE PROTEINASES; DOWN-REGULATION; BREAST-CANCER; MATRIX METALLOPROTEINASES; PROTEOLYTIC ENZYME;
D O I
10.1517/14728222.2013.740461
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Introduction: Cathepsin B is of significant importance to cancer therapy as it is involved in various pathologies and oncogenic processes in humans. Numerous studies have shown that abnormal regulation of cathepsin B overexpression is correlated with invasive and metastatic phenotypes in cancers. Cathepsin B is normally associated with the lysosomes involved in autophagy and immune response, but its aberrant expression has been shown to lead to cancers. Areas covered: This review highlights the oncogenic role of cathepsin B, discusses the regulation of cathepsin B in light of oncogenesis, discusses the role of cathepsin B as a signaling molecule, and highlights the therapeutic potential of targeting cathepsin B. Expert opinion: Targeting cathepsin B alone does not appear to abolish tumor growth, and this is probably because cathepsin B appears to have diverse functions and influence numerous pathways. It is not clear whether global suppression of cathepsin B activity or expression would produce unintended effects or cause the activation or suppression of unwanted pathways. A localized approach for targeting the expression of cathepsin B would be more relevant. Moreover, a combination of targeting cathepsin B with other relevant oncogenic molecules has significant therapeutic potential.
引用
收藏
页码:281 / 291
页数:11
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