Immunoproteasome in Cancer and Neuropathologies: A New Therapeutic Target?

被引:26
作者
Bellavista, Elena [1 ,2 ]
Andreoli, Federico [2 ]
Parenti, Marco Daniele [2 ]
Martucci, Morena [1 ,2 ]
Santoro, Aurelia [2 ]
Salvioli, Stefano [1 ,2 ]
Capri, Miriam [1 ,2 ]
Baruzzi, Agostino [3 ,4 ]
Del Rio, Alberto [2 ]
Franceschi, Claudio [1 ,2 ]
Mishto, Michele [1 ,5 ]
机构
[1] Interdept Ctr Studies Biophys Bioinformat & Bioco, I-40126 Bologna, Italy
[2] Univ Bologna, Dept Expt Pathol, I-40126 Bologna, Italy
[3] Univ Bologna, Dept Neurol Sci, I-40123 Bologna, Italy
[4] Univ Bologna, IRCCS Inst Neurol Sci, I-40123 Bologna, Italy
[5] Charite, Inst Biochem, D-13347 Berlin, Germany
关键词
Immunoproteasome; standard proteasome; selective inhibitor; immunoproteasome model; proteasome enhancers; computer-aided drug design; cancer; tumour; brain; epilepsy; multiple sclerosis; Alzheimer's disease; T-CELL RESPONSES; STRUCTURE-BASED DESIGN; MYELIN BASIC-PROTEIN; CLASS-I MOLECULES; PROTEASOME INHIBITORS; 20S PROTEASOME; ALZHEIMERS-DISEASE; MULTIPLE-SCLEROSIS; ANTIGEN PRESENTATION; SELECTIVE INHIBITOR;
D O I
10.2174/138161213804581927
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Immunoproteasome is an emerging biological target that constitutes a key element not only in antigen presentation but also in T cell and cytokine regulation as well as cellular homeostasis. Respect to standard proteasome, the inducible expression and different sensitivity towards activity modulators of immunoproteasome render it a potential therapeutic target for tumours and central nervous system diseases. In this review we report the cutting edge studies for understanding when immunoproteasome expression is induced and how it regulates pivotal pathways involved in tumours and neuropathologies, including apoptosis and inflammation. We emphasize its role as a new pharmacological target by describing the recent medicinal chemistry efforts aimed at design selective small-molecule modulators of both standard- and immuno-proteasome forms. Finally, we also present an in silico model of the human immunoproteasome structure by the major molecular differences with the 20S standard proteasome and discuss the perspective for the design of novel specific small-molecule modulators for the different proteasome isoforms.
引用
收藏
页码:702 / 718
页数:17
相关论文
共 164 条
[1]   The proteasome: A suitable antineoplastic target [J].
Adams, J .
NATURE REVIEWS CANCER, 2004, 4 (05) :349-360
[2]   Pyrimidinylimidazole inhibitors of CSBP/P37 kinase demonstrating decreased inhibition of hepatic cytochrome P450 enzymes [J].
Adams, JL ;
Boehm, JC ;
Kassis, S ;
Gorycki, PD ;
Webb, EF ;
Hall, R ;
Sorenson, M ;
Lee, JC ;
Ayrton, A ;
Griswold, DE ;
Gallagher, TF .
BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, 1998, 8 (22) :3111-3116
[3]   Effects of PS-341 on the activity and composition of proteasomes in multiple myeloma cells [J].
Altun, M ;
Galardy, PJ ;
Shringarpure, R ;
Hideshima, T ;
LeBlanc, R ;
Anderson, KC ;
Ploegh, HL ;
Kessler, BM .
CANCER RESEARCH, 2005, 65 (17) :7896-7901
[4]  
[Anonymous], 2011, SITEMAP
[5]   A new structural class of proteasome inhibitors identified by microbial screening using yeast-based assay [J].
Asai, A ;
Tsujita, T ;
Sharma, SV ;
Yamashita, Y ;
Akinaga, S ;
Funakoshi, M ;
Kobayashi, H ;
Mizukami, T .
BIOCHEMICAL PHARMACOLOGY, 2004, 67 (02) :227-234
[6]   Belactosin A, a novel antitumor antibiotic acting on cyclin/CDK mediated cell cycle regulation, produced by Streptomyces sp. [J].
Asai, A ;
Hasegawa, A ;
Ochiai, K ;
Yamashita, Y ;
Mizukami, T .
JOURNAL OF ANTIBIOTICS, 2000, 53 (01) :81-83
[7]  
Barbosa AJ, 2012, CURRENT TOP IN PRESS
[8]  
Basler M, 2011, J IMMUNOL
[9]   Prevention of Experimental Colitis by a Selective Inhibitor of the Immunoproteasome [J].
Basler, Michael ;
Dajee, Maya ;
Moll, Carlo ;
Groettrup, Marcus ;
Kirk, Christopher J. .
JOURNAL OF IMMUNOLOGY, 2010, 185 (01) :634-641
[10]   Novel Organic Proteasome Inhibitors Identified by Virtual and in Vitro Screening [J].
Basse, Nicolas ;
Montes, Matthieu ;
Marechal, Xavier ;
Qin, Lixian ;
Bouvier-Durand, Michelle ;
Genin, Emilie ;
Vidal, Joelle ;
Villoutreix, Bruno O. ;
Reboud-Ravaux, Michele .
JOURNAL OF MEDICINAL CHEMISTRY, 2010, 53 (01) :509-513