The Ubiquitin-Proteasome System (UPS) and the Mechanism of Action of Bortezomib

被引:41
作者
Cvek, Boris [1 ]
Dvorak, Zdenek [1 ]
机构
[1] Palacky Univ, Fac Sci, Dept Cell Biol & Genet, Olomouc 78371, Czech Republic
关键词
Ubiquitin-proteasome system; bortezomib; mechanism of action; FACTOR-KAPPA-B; ENDOPLASMIC-RETICULUM STRESS; LUNG-CANCER CELLS; PHASE-I TRIAL; INHIBITORS INDUCE APOPTOSIS; PHARMACODYNAMIC END-POINTS; UNFOLDED PROTEIN RESPONSE; 19S REGULATORY PARTICLES; METASTATIC BREAST-CANCER; MYELOMA BONE-DISEASE;
D O I
10.2174/138161211796197124
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Proteasome inhibition is a modern and surprisingly successful approach how to cancer treatment. Bortezomib(Velcade (R)) is a first-in-class proteasome inhibitor and has been approved for first-line treatment of multiple myeloma and second-line treatment of mantle cell lymphoma. There have been almost 200 clinical trials with bortezomib, both as a single agent and in combination with other drugs, for various cancers, as listed in the US National Cancer Institute database. However, bortezomib's mechanism of action remains elusive despite enormous progress in our knowledge of the cell biology of the ubiquitin-proteasome system (UPS) and bortezomib-induced signaling events in cancer cells. This review maps a rapidly growing and open body of research in both areas.
引用
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页码:1483 / 1499
页数:17
相关论文
共 383 条
[1]  
Adams J, 1999, CANCER RES, V59, P2615
[2]   Development of the proteasome inhibitor PS-341 [J].
Adams, J .
ONCOLOGIST, 2002, 7 (01) :9-16
[3]   Development of the proteasome inhihitor Veleade™ (Bortezomib) [J].
Adams, J ;
Kauffman, M .
CANCER INVESTIGATION, 2004, 22 (02) :304-311
[4]   The proteasome: A suitable antineoplastic target [J].
Adams, J .
NATURE REVIEWS CANCER, 2004, 4 (05) :349-360
[5]   Novel inhibitors of the proteasome and their therapeutic use in inflammation [J].
Adams, J ;
Stein, R .
ANNUAL REPORTS IN MEDICINAL CHEMISTRY, VOL 31, 1996, 31 :279-288
[6]   Potent and selective inhibitors of the proteasome: Dipeptidyl boronic acids [J].
Adams, J ;
Behnke, M ;
Chen, SW ;
Cruickshank, AA ;
Dick, LR ;
Grenier, L ;
Klunder, JM ;
Ma, YT ;
Plamondon, L ;
Stein, RL .
BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, 1998, 8 (04) :333-338
[7]   The development of proteasome inhibitors as anticancer drugs [J].
Adams, J .
CANCER CELL, 2004, 5 (05) :417-421
[8]  
Adams J, 1996, CHEM ABSTR, Patent No. 96/13266
[9]  
Aghajanian C, 2002, CLIN CANCER RES, V8, P2505
[10]   A phase II evaluation of bortezomib in the treatment of recurrent platinum-sensitive ovarian or primary peritoneal cancer: A Gynecologic Oncology Group study [J].
Aghajanian, Carol ;
Blessing, John A. ;
Darcy, Kathleen M. ;
Reid, Gary ;
DeGeest, Koen ;
Rubin, Stephen C. ;
Mannel, Robert S. ;
Rotmensch, Jacob ;
Schilder, Russell J. ;
Riordan, William .
GYNECOLOGIC ONCOLOGY, 2009, 115 (02) :215-220