Cysteine cathepsin proteases as pharmacological targets in cancer

被引:242
作者
Palermo, Carmela [1 ]
Joyce, Johanna A. [1 ]
机构
[1] Mem Sloan Kettering Canc Ctr, Ctr Biol & Genet Program, New York, NY 10021 USA
关键词
D O I
10.1016/j.tips.2007.10.011
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Proteolytic activity is required for several key pro-tumorigenic processes: angiogenesis, invasion and metastasis. Consequently, increases in protease expression and activity are frequently reported in human cancers, and correlate with malignant progression and poor patient prognosis. Cysteine cathepsin proteases have recently emerged as an important class of proteolytic enzymes in cancer development, and cysteine cathepsin inhibitors have been proposed as anticancer agents. In this review, we highlight recent studies that now allow us to evaluate critically whether cysteine cathepsin inhibition represents a viable therapeutic strategy for the treatment of cancer.
引用
收藏
页码:22 / 28
页数:7
相关论文
共 62 条
[1]   Schistosomiasis mansoni: Novel chemotherapy using a cysteine protease inhibitor [J].
Abdulla, Maha-Hamadien ;
Lim, Kee-Chong ;
Sajid, Mohammed ;
McKerrow, James H. ;
Caffrey, Conor R. .
PLOS MEDICINE, 2007, 4 (01) :130-138
[2]   Inhibition of cysteine cathepsin protease activity enhances chemotherapy regimens by decreasing tumor growth and invasiveness in a mouse model of multistage cancer [J].
Bell-McGuinn, Katherine M. ;
Garfall, Alfred L. ;
Bogyo, Matthew ;
Hanahan, Douglas ;
Joyce, Johanna A. .
CANCER RESEARCH, 2007, 67 (15) :7378-7385
[3]   Cysteine proteases as disease markers [J].
Berdowska, I .
CLINICA CHIMICA ACTA, 2004, 342 (1-2) :41-69
[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]   BACTERIAL-GROWTH BLOCKED BY A SYNTHETIC PEPTIDE BASED ON THE STRUCTURE OF A HUMAN PROTEINASE-INHIBITOR [J].
BJORCK, L ;
AKESSON, P ;
BOHUS, M ;
TROJNAR, J ;
ABRAHAMSON, M ;
OLAFSSON, I ;
GRUBB, A .
NATURE, 1989, 337 (6205) :385-386
[6]   Noninvasive optical imaging of cysteine protease activity using fluorescently quenched activity-based probes [J].
Blum, Galia ;
von Degenfeld, Georges ;
Merchant, Milton J. ;
Blau, Helen M. ;
Bogyo, Matthew .
NATURE CHEMICAL BIOLOGY, 2007, 3 (10) :668-677
[7]   The role of disturbed pH dynamics and the Na+/H+ exchanger in metastasis [J].
Cardone, RA ;
Casavola, V ;
Reshkin, SJ .
NATURE REVIEWS CANCER, 2005, 5 (10) :786-795
[8]   Inhibition of spinal microglial cathepsin S for the reversal of neuropathic pain [J].
Clark, Anna K. ;
Yip, Ping K. ;
Grist, John ;
Gentry, Clive ;
Staniland, Amelia A. ;
Marchand, Fabien ;
Dehvari, Maliheh ;
Wotherspoon, Glen ;
Winter, Janet ;
Ullah, Jakir ;
Bevan, Stuart ;
Malcangio, Marzia .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2007, 104 (25) :10655-10660
[9]   Cancer therapy - Matrix metalloproteinase inhibitors and cancer: Trials and tribulations [J].
Coussens, LM ;
Fingleton, B ;
Matrisian, LM .
SCIENCE, 2002, 295 (5564) :2387-2392
[10]   Biochemical markers of bone turnover in the clinical development of drugs for osteoporosis and metastatic bone disease - Potential uses and pitfalls [J].
Cremers, Serge ;
Garnero, Patrick .
DRUGS, 2006, 66 (16) :2031-2058