Proteasome inhibitors as new anticancer drugs

被引:135
作者
Adams, J [1 ]
机构
[1] Millennium Pharmaceut, Cambridge, MA 02139 USA
关键词
D O I
10.1097/00001622-200211000-00007
中图分类号
R73 [肿瘤学];
学科分类号
100214 [肿瘤学];
摘要
The targeted degradation of key regulatory proteins is an essential element of cell cycle control. The proteasome plays a central role in the degradation of such proteins and has therefore become an important therapeutic target for diseases involving cell proliferation, notably cancer. This review summarizes numerous studies demonstrating that proteasome inhibition induces apoptosis and sensitizes cancer cells to traditional tumoricidal agents both in vitro and in vivo. The potent and selective proteasome inhibitor, PS-341, is particularly promising from a therapeutic perspective, and it is the only such inhibitor that has progressed to clinical trials. Preliminary data indicate that the drug is well tolerated by patients with cancer, and further trials are underway to assess the safety and efficacy of proteasome inhibition in hematologic and solid tumors, both as a monotherapy and in combination with other chemotherapeutics. (C) 2002 Lippincott Williams Wilkins, Inc.
引用
收藏
页码:628 / 634
页数:7
相关论文
共 60 条
[1]
Adams J, 1999, CANCER RES, V59, P2615
[2]
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
[3]
Proteasome inhibitor-induced apoptosis of B-chronic lymphocytic leukaemia cells involves cytochrome c release and caspase activation, accompanied by formation of an ∼700 kDa Apaf-1 containing apoptosome complex [J].
Almond, JB ;
Snowden, RT ;
Hunter, A ;
Dinsdale, D ;
Cain, K ;
Cohen, GM .
LEUKEMIA, 2001, 15 (09) :1388-1397
[4]
Protease inhibitor-induced apoptosis:: accumulation of wt p53, p21WAF1/CIP1 and induction of apoptosis are independent markers of proteasome inhibition [J].
An, WG ;
Hwang, SG ;
Trepel, JB ;
Blagosklonny, MV .
LEUKEMIA, 2000, 14 (07) :1276-1283
[5]
Covalent modification of the active site threonine of proteasomal beta subunits and the Escherichia coli homolog HslV by a new class of inhibitors [J].
Bogyo, M ;
McMaster, JS ;
Gaczynska, M ;
Tortorella, D ;
Goldberg, AL ;
Ploegh, H .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1997, 94 (13) :6629-6634
[6]
Chemosensitization of pancreatic cancer by inhibition of the 26S proteasome [J].
Bold, RJ ;
Virudachalam, S ;
McConkey, DJ .
JOURNAL OF SURGICAL RESEARCH, 2001, 100 (01) :11-17
[7]
The Rel/NF-κB family directly activates expression of the apoptosis inhibitor Bcl-xL [J].
Chen, CL ;
Edelstein, LC ;
Gélinas, C .
MOLECULAR AND CELLULAR BIOLOGY, 2000, 20 (08) :2687-2695
[8]
CLARK JW, 2002, P AN M AM SOC CLIN, V21, pA93
[9]
Cusack JC, 2001, CANCER RES, V61, P3535
[10]
NF-κB and chemoresistance:: potentiation of cancer chemotherapy via inhibition of NF-κB [J].
Cusack, JC ;
Liu, R ;
Baldwin, AS .
DRUG RESISTANCE UPDATES, 1999, 2 (04) :271-273