Proteasome Regulators: Activators and Inhibitors

被引:84
作者
Huang, Li [1 ]
Chen, Chin Ho [1 ]
机构
[1] Duke Univ, Med Ctr, Dept Surg, Durham, NC 27710 USA
关键词
Proteasome; activator; inhibitor; natural products; betulinic acids; peptides; anti-cancer; bortezomib; IMMUNODEFICIENCY-VIRUS TYPE-1; NF-KAPPA-B; INTRACELLULAR PROTEIN-DEGRADATION; BETULINIC ACID; MULTICATALYTIC PROTEINASE; MULTIPLE-MYELOMA; 20S PROTEASOME; STREPTOMYCES SP; CANCER CELLS; IN-VITRO;
D O I
10.2174/092986709787581860
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
This mini review covers the drug discovery aspect of both proteasome activators and inhibitors. The proteasome is involved in many essential cellular functions, such as regulation of cell cycle, cell differentiation, signal transduction pathways, antigen processing for appropriate immune responses, stress signaling, inflammatory responses, and apoptosis. Due to the importance of the proteasome in cellular functions, inhibition or activation of the proteasome could become a useful therapeutic strategy for a variety of diseases. Many proteasome inhibitors have been identified and can be classified into two groups according to their source: chemically synthesized small molecules and compounds derived from natural products. A successful example of development of a proteasome inhibitor as a clinically useful drug is the peptide boronate, PS341 (Bortezomib), was approved for the treatment of multiple myeloma. In contrast to proteasome inhibitors, small molecules that can activate or enhance proteasome activity are rare and are not well studied. The fact that overexpression of the cellular proteasome activator PA28 exhibited beneficial effects on the Huntington's disease neuronal model cells raised the prospect that small molecule proteasome activators could become useful therapeutics. The beneficial effect of oleuropein, a small molecule proteasome activator, on senescence of human fibroblasts also suggested that proteasome activators might have the potential to be developed into anti-aging agents.
引用
收藏
页码:931 / 939
页数:9
相关论文
共 94 条
[1]   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
[2]   Molecular Basis for Proline- and Arginine-Rich Peptide Inhibition of Proteasome [J].
Anbanandam, Asokan ;
Albarado, Diana C. ;
Tirziu, Daniela C. ;
Simons, Michael ;
Veeraraghavan, Sudha .
JOURNAL OF MOLECULAR BIOLOGY, 2008, 384 (01) :219-227
[3]   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
[4]   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
[5]   20S proteasome and its inhibitors: Crystallographic knowledge for drug development [J].
Borissenko, Ljudmila ;
Groll, Michael .
CHEMICAL REVIEWS, 2007, 107 (03) :687-717
[6]   Ubiquitin-mediated degradation of the proapoptotic active form of bid - A functional consequence on apoptosis induction [J].
Breitschopf, K ;
Zeiher, AM ;
Dimmeler, S .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (28) :21648-21652
[7]   Targeting mitochondria to overcome conventional and bortezomib/proteasome inhibitor PS-341 resistance in multiple myeloma (MM) cells [J].
Chauhan, D ;
Li, GL ;
Podar, K ;
Hideshima, T ;
Mitsiades, C ;
Schlossman, R ;
Munshi, N ;
Richardson, P ;
Cotter, FE ;
Anderson, KC .
BLOOD, 2004, 104 (08) :2458-2466
[8]   Proteolysis: from the lysosome to ubiquitin and the proteasome [J].
Ciechanover, A .
NATURE REVIEWS MOLECULAR CELL BIOLOGY, 2005, 6 (01) :79-86
[9]   IN-VITRO ACTIVATION OF THE 20S PROTEASOME [J].
DAHLMANN, B ;
BECHER, B ;
SOBEK, A ;
EHLERS, C ;
KOPP, F ;
KUEHN, L .
ENZYME & PROTEIN, 1993, 47 (4-6) :274-284
[10]   ACTIVATION OF THE MULTICATALYTIC PROTEINASE FROM RAT SKELETAL-MUSCLE BY FATTY-ACIDS OR SODIUM DODECYL-SULFATE [J].
DAHLMANN, B ;
RUTSCHMANN, M ;
KUEHN, L ;
REINAUER, H .
BIOCHEMICAL JOURNAL, 1985, 228 (01) :171-177