Destination 'Lysosome':: a target organelle for tumour cell killing?

被引:68
作者
Castino, R [1 ]
Démoz, M [1 ]
Isidoro, C [1 ]
机构
[1] Univ A Avogadro, Dipartimento Sci Med, Lab Patol Mol, I-28100 Novara, Italy
关键词
cathepsins; cell death; antiblastic drugs; cancer;
D O I
10.1002/jmr.643
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Lysosomes and lysosome-related organelles constitute a system of acid compartments that interconnect the inside of the cell with the extracellular environment via endocytosis, phagocytosis and exocytosis. In recent decades it has been recognized that lysosomes are not just wastebaskets for disposal of unused cellular constituents, but that they are involved in several cellular processes such as post-translational maturation of proteins, degradation of receptors and extracellular release of active enzymes. By complementing the autophagic process, lysosomes actively contribute to the maintenance of cellular homeostasis. Proteolysis by lysosomal cathepsins has been shown to mediate the death signal of cytotoxic drugs and cytokines, as well as the activation of pro-survival factors. Secreted lysosomal cathepsins have been shown to degrade protein components of the extracellular matrix, thus contributing actively to its re-modelling in physiological and pathological processes. The malfunction of lysosomes can, therefore, impact on cell behaviour and fate. Here we review the role of lysosomal hydrolases in several aspects of the malignant phenotype including loss of cell growth control, altered regulation of cell death, acquisition of chemoresistance and of metastatic potential. Based on these observations, the lysosome is proposed as a potential target organelle for the chemotherapy of tumours. We will also present some recent data concerning the technologies for delivering chemotherapeutic drugs to the endosomal-lysosomal compartment and the strategies to improve their efficacy. Copyright (C) 2003 John Wiley Sons, Ltd.
引用
收藏
页码:337 / 348
页数:14
相关论文
共 186 条
[71]   Synthesis, maturation and extracellular release of procathepsin D as influenced by cell proliferation or transformation [J].
Isidoro, C ;
Demoz, M ;
DeStefanis, D ;
Baccino, FM ;
Bonelli, G .
INTERNATIONAL JOURNAL OF CANCER, 1995, 63 (06) :866-871
[72]  
Isidoro C, 1997, INT J CANCER, V70, P310, DOI 10.1002/(SICI)1097-0215(19970127)70:3<310::AID-IJC11>3.0.CO
[73]  
2-J
[74]  
Isidoro C, 1997, CELL GROWTH DIFFER, V8, P1029
[75]  
Isidoro C, 1997, INT J CANCER, V70, P561, DOI 10.1002/(SICI)1097-0215(19970304)70:5<561::AID-IJC12>3.0.CO
[76]  
2-G
[77]   Taking the study of cancer cell survival to a new dimension [J].
Jacks, T ;
Weinberg, RA .
CELL, 2002, 111 (07) :923-925
[78]   Membrane proximal lysosomes are the major vesicles responsible for calcium-dependent exocytosis in nonsecretory cells [J].
Jaiswal, JK ;
Andrews, NW ;
Simon, SM .
JOURNAL OF CELL BIOLOGY, 2002, 159 (04) :625-635
[79]   Inhibition of autophagy abrogates tumour necrosis factor alpha induced apoptosis in human T-lymphoblastic leukaemic cells [J].
Jia, L ;
Dourmashkin, RR ;
Allen, PD ;
Gray, AB ;
Newland, AC ;
Kelsey, SM .
BRITISH JOURNAL OF HAEMATOLOGY, 1997, 98 (03) :673-685
[80]   Sphingosine-induced apoptosis is dependent on lysosomal proteases [J].
Kågedal, K ;
Zhao, M ;
Svensson, I ;
Brunk, UT .
BIOCHEMICAL JOURNAL, 2001, 359 (02) :335-343