Proteasome inhibitors:: antitumor effects and beyond

被引:191
作者
Nencioni, A.
Gruenebach, F.
Patrone, F.
Ballestrero, A.
Brossart, P.
机构
[1] Univ Tubingen, Dept Hematol Oncol & Immunol, D-72076 Tubingen, Germany
[2] Univ Genoa, Dept Internal Med, I-16126 Genoa, Italy
关键词
proteasome inhibitors; apoptosis; immunomodulation; dendritic cells;
D O I
10.1038/sj.leu.2404444
中图分类号
R73 [肿瘤学];
学科分类号
100214 [肿瘤学];
摘要
Proteasome inhibitors are emerging as effective drugs for the treatment of multiple myeloma and possibly certain subtypes of non-Hodgkin's lymphoma. Bortezomib (Velcade) is the first proteasome inhibitor proven to be clinically useful and will soon be followed by a second generation of small molecule inhibitors with improved pharmacological properties. Although it is now understood that certain types of malignancies have an exquisite dependence on a functional proteasome for their survival, the underlying reason(s) remain unclear as of now. In this context, addiction to nuclear factor-kappa B (NF-kappa B)-induced survival signals, activation of the unfolded protein response as well as a reduced proteasomal activity in differentiated plasma cells have all been proposed to justify proteasome inhibitors' activity in susceptible tissues. In addition to their anticancer properties, bortezomib and related drugs modulate inflammatory and immune responses by affecting function and survival of immune cells such as lymphocytes and dendritic cells. The present review offers an overview of the biological effects that have been involved in proteasome inhibitors' antitumor activity and suggests prospective future applications for these drugs based on their recently characterized anti-inflammatory and immunomodulatory effects.
引用
收藏
页码:30 / 36
页数:7
相关论文
共 66 条
[1]
The proteasome: A suitable antineoplastic target [J].
Adams, J .
NATURE REVIEWS CANCER, 2004, 4 (05) :349-360
[2]
The development of proteasome inhibitors as anticancer drugs [J].
Adams, J .
CANCER CELL, 2004, 5 (05) :417-421
[3]
Dendritic cells and autoimmunity [J].
Bayry, J ;
Thirion, M ;
Delignat, S ;
Misra, N ;
Lacroix-Desmazes, S ;
Kazatchkine, MD ;
Kaveri, SV .
AUTOIMMUNITY REVIEWS, 2004, 3 (03) :183-187
[4]
Phase I/II trial assessing bortezomlb and melphalan combination therapy for the treatment of patients with relapsed or refractory multiple myeloma [J].
Berenson, JR ;
Yang, HH ;
Sadler, K ;
Jarutirasarn, SG ;
Vescio, RA ;
Mapes, R ;
Purner, M ;
Lee, SP ;
Wilson, J ;
Morrison, B ;
Adams, J ;
Schenkein, D ;
Swift, R .
JOURNAL OF CLINICAL ONCOLOGY, 2006, 24 (06) :937-944
[5]
Bortezomib induces selective depletion of alloreactive T lymphocytes and decreases the production of Th1 cytokines [J].
Blanco, B ;
Pérez-Simón, JA ;
Sánchez-Abarca, LI ;
Carvajal-Vergara, X ;
Mateos, J ;
Vidriales, B ;
López-Holgado, N ;
Maiso, P ;
Alberca, M ;
Villarón, E ;
Schenkein, D ;
Pandiella, A ;
San Miguel, J .
BLOOD, 2006, 107 (09) :3575-3583
[6]
Loss of the cylindromatosis tumour suppressor inhibits apoptosis by activating NF-κB [J].
Brummelkamp, TR ;
Nijman, SMB ;
Dirac, AMG ;
Bernards, R .
NATURE, 2003, 424 (6950) :797-801
[7]
Progressively impaired proteasomal capacity during terminal plasma cell differentiation [J].
Cenci, S ;
Mezghrani, A ;
Cascio, P ;
Bianchi, G ;
Cerruti, F ;
Fra, A ;
Lelouard, H ;
Masciarelli, S ;
Mattioli, L ;
Oliva, L ;
Orsi, A ;
Pasqualetto, E ;
Pierre, P ;
Ruffato, E ;
Tagliavacca, L ;
Sitia, R .
EMBO JOURNAL, 2006, 25 (05) :1104-1113
[8]
A novel orally active proteasome inhibitor induces apoptosis in multiple myeloma cells with mechanisms distinct from Bortezomib [J].
Chauhan, D ;
Catley, L ;
Li, GL ;
Podar, K ;
Hideshima, T ;
Velankar, M ;
Mitsiades, C ;
Mitsiades, N ;
Yasui, H ;
Letai, A ;
Ovaa, H ;
Berkers, C ;
Nicholson, B ;
Chao, TH ;
Neuteboom, STC ;
Richardson, P ;
Palladino, MA ;
Anderson, KC .
CANCER CELL, 2005, 8 (05) :407-419
[9]
Dendritic cell apoptosis in the maintenance of immune tolerance [J].
Chen, M ;
Wang, YH ;
Wang, YH ;
Huang, L ;
Sandoval, H ;
Liu, YJ ;
Wang, J .
SCIENCE, 2006, 311 (5764) :1160-1164
[10]
Proteasome-inhibited dendritic cells demonstrate improved presentation of exogenous synthetic and natural HLA-class I peptide epitopes [J].
Chromik, J ;
Schnürer, E ;
Meyer, RG ;
Wehler, T ;
Tüting, T ;
Wölfel, T ;
Huber, C ;
Herr, W .
JOURNAL OF IMMUNOLOGICAL METHODS, 2006, 308 (1-2) :77-89