Mitogen-activated protein kinases as therapeutic targets in osteoarthritis

被引:119
作者
Loeser, Richard F. [1 ]
Erickson, Elizabeth A. [1 ]
Long, David L. [1 ]
机构
[1] Wake Forest Univ, Bowman Gray Sch Med, Sect Mol Med, Dept Internal Med, Winston Salem, NC 27157 USA
关键词
articular cartilage; mitogen-activated protein kinases; osteoarthritis therapy;
D O I
10.1097/BOR.0b013e3283090463
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Purpose of review The mitogen-activated protein (MAP) kinases are intracellular signaling proteins which play a central role in controlling the activity of pathways that regulate production and activity of multiple mediators of joint tissue destruction. The therapeutic potential of MAP kinase inhibition in osteoarthritis was reviewed. Recent findings Results from basic research studies support the role of MAP kinases as central mediators that regulate expression of proinflammatory cytokines and metalloproteinases but also as potential pain mediators as well. Cell culture and animal model studies suggest that inhibition of MAP kinases might slow progression of osteoarthritis but trials of MAP kinase inhibitors in humans with osteoarthritis have not yet been reported. Safety concerns of the currently available inhibitors have limited their initial use to trials in conditions considered more severe than osteoarthritis. Summary MAP kinase inhibition has the potential to slow disease progression in osteoarthritis and also might reduce pain; however, safety concerns have limited the use of general MAP kinase inhibitors in humans. Further understanding of the function of specific isoforms of the MAP kinases as well as upstream and downstream effectors may lead to the development of more specific inhibitors with less toxicity that could eventually be used as structure-modifying drugs for osteoarthritis.
引用
收藏
页码:581 / 586
页数:6
相关论文
共 48 条
[1]   Peroxisome proliferator-activated receptor γ1 expression is diminished in human osteoarthritic cartilage and is downregulated by interleukin-1β in articular chondrocytes [J].
Afif, Hassan ;
Benderdour, Mohamed ;
Mfuna-Endam, Leandra ;
Martel-Pelletier, Johanne ;
Pelletier, Jean-Pierre ;
Duval, Nicholas ;
Fahmi, Hassan .
ARTHRITIS RESEARCH & THERAPY, 2007, 9 (02)
[2]   Large-scale gene expression profiling reveals major pathogenetic pathways of cartilage degeneration in osteoarthritis [J].
Aigner, Thomas ;
Fundel, Katrin ;
Saas, Joachim ;
Gebhard, Pia M. ;
Haag, Jochen ;
Weiss, Tilo ;
Zien, Alexander ;
Obermayr, Franz ;
Zimmer, Ralf ;
Bartnik, Eckart .
ARTHRITIS AND RHEUMATISM, 2006, 54 (11) :3533-3544
[3]   MAP kinase pathways: The first twenty years [J].
Avruch, Joseph .
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR CELL RESEARCH, 2007, 1773 (08) :1150-1160
[4]  
Badger AM, 2000, ARTHRITIS RHEUM, V43, P175, DOI 10.1002/1529-0131(200001)43:1<175::AID-ANR22>3.0.CO
[5]  
2-S
[6]   Toll-like receptors and chondrocytes - The lipopolysaccharide-induced decrease in cartilage matrix synthesis is dependent on the presence of Toll-like receptor 4 and antagonized by bone morphogenetic protein 7 [J].
Bobacz, K. ;
Sunk, I. G. ;
Hofstaetter, J. G. ;
Amoyo, L. ;
Toma, C. D. ;
Akira, S. ;
Weichhart, T. ;
Saemann, M. ;
Smolen, J. S. .
ARTHRITIS AND RHEUMATISM, 2007, 56 (06) :1880-1893
[7]   Therapeutic promise of JNK ATP-noncompetitive inhibitors [J].
Bogoyevitch, MA .
TRENDS IN MOLECULAR MEDICINE, 2005, 11 (05) :232-239
[8]   PD-0200347, an α2δ ligand of the voltage gated calcium channel, inhibits in vivo activation of the Erk1/2 pathway in osteoarthritic chondrocytes:: a PKCα dependent effect [J].
Boileau, C ;
Martel-Pelletier, J ;
Brunet, J ;
Schrier, D ;
Flory, C ;
Boily, M ;
Pelletier, JP .
ANNALS OF THE RHEUMATIC DISEASES, 2006, 65 (05) :573-580
[9]   Oral treatment with PD-0200347, an α2δ ligand, reduces the development of experimental osteoarthritis by inhibiting metalloproteinases and inducible nitric oxide synthase gene expression and synthesis in cartilage chondrocytes [J].
Boileau, C ;
Martel-Pelletier, J ;
Brunet, J ;
Tardif, G ;
Schrier, D ;
Flory, C ;
El-Kattan, A ;
Boily, M ;
Pelletier, JP .
ARTHRITIS AND RHEUMATISM, 2005, 52 (02) :488-500
[10]   Activation of the extracellular signal-regulated kinase in the amygdala modulates pain perception [J].
Carrasquillo, Yarimar ;
Gereau, Robert W. .
JOURNAL OF NEUROSCIENCE, 2007, 27 (07) :1543-1551