Signal transduction pathways: new targets for treating rheumatoid arthritis

被引:56
作者
Morel, J
Berenbaum, F
机构
[1] CHU Lapeyronie Hosp, Immunorheumatol Dept, F-34295 Montpellier 5, France
[2] CHU Lapeyronie Hosp, INSERM, U 454, F-34295 Montpellier 5, France
[3] Univ Paris 06, St Antoine Hosp, CNRS, Dept Rheumatol, Paris, France
[4] Univ Paris 06, St Antoine Hosp, CNRS, UMR 7079, Paris, France
关键词
signal transduction pathways; pharmacological inhibitors; anti-sense oligonucleotides; rheumatoid arthritis; inflammation; gene therapy; mitogen-activated protein kinase; suppressors of cytokine signaling;
D O I
10.1016/j.jbspin.2004.03.004
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Biotherapies and other new treatments introduced over the last few years have considerably enriched the therapeutic armamentarium for rheumatoid arthritis. Nevertheless, primary refractoriness or secondary escape phenomenon may occur, indicating a need for identifying new treatment targets. Promising candidates can be found among compounds involved in signal transduction pathways, most notably protein kinases (mitogen-activated protein kinase, MAPK and phosphatidylinositol-3 protein kinase, PI3) and transcription factors (nuclear factor kappa B. NF-kappaB activating protein 1, AP-1; CCAAT/enhancer-binding protein, C/EB.P and signal transducer and activator of transcription, STAT). Inhibition of signal transduction pathways may be achievable via three main strategies: pharmacological inhibitors, anti-sense or more specific inhibitors such as oligionucleotides or interfering mRNA, and induced overexpression of naturally occurring inhibitors. Clinical trials are under way to evaluate pharmacological inhibitors such as p38 MAPK. Although the preliminary results are promising, proof of safety has not yet been obtained. Signal transduction pathways are involved in normal processes, whose inhibition might produce untoward effects. (C) 2004 Elsevier SAS. All rights reserved.
引用
收藏
页码:503 / 510
页数:8
相关论文
共 63 条
[21]  
Han ZN, 1999, J PHARMACOL EXP THER, V291, P124
[22]  
Han ZN, 2001, J CLIN INVEST, V108, P73, DOI 10.1172/JCI12466
[23]   p38 MAPK signalling cascades in inflammatory disease [J].
Herlaar, E ;
Brown, Z .
MOLECULAR MEDICINE TODAY, 1999, 5 (10) :439-447
[24]   Cancer research - A surprising function for the PTEN tumor suppressor [J].
Hopkin, K .
SCIENCE, 1998, 282 (5391) :1027-+
[25]   Tumor necrosis factor receptor-associated factor (TRAF) family: Adapter proteins that mediate cytokine signaling [J].
Inoue, J ;
Ishida, T ;
Tsukamoto, N ;
Kobayashi, N ;
Naito, A ;
Azuma, S ;
Yamamoto, T .
EXPERIMENTAL CELL RESEARCH, 2000, 254 (01) :14-24
[26]   Necessary role of phosphatidylinositol 3-kinase in transforming growth factor β-mediated activation of Akt in normal and rheumatoid arthritis synovial fibroblasts [J].
Kim, G ;
Jun, JB ;
Elkon, KB .
ARTHRITIS AND RHEUMATISM, 2002, 46 (06) :1504-1511
[27]   Tumor suppressor MMAC/PTEN inhibits cytokine-induced NFκB activation without interfering with the IκB degradation pathway [J].
Koul, D ;
Yao, YX ;
Abbruzzese, JL ;
Yung, WKA ;
Reddy, SAG .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2001, 276 (14) :11402-11408
[28]   A PROTEIN-KINASE INVOLVED IN THE REGULATION OF INFLAMMATORY CYTOKINE BIOSYNTHESIS [J].
LEE, JC ;
LAYDON, JT ;
MCDONNELL, PC ;
GALLAGHER, TF ;
KUMAR, S ;
GREEN, D ;
MCNULTY, D ;
BLUMENTHAL, MJ ;
HEYS, JR ;
LANDVATTER, SW ;
STRICKLER, JE ;
MCLAUGHLIN, MM ;
SIEMENS, IR ;
FISHER, SM ;
LIVI, GP ;
WHITE, JR ;
ADAMS, JL ;
YOUNG, PR .
NATURE, 1994, 372 (6508) :739-746
[29]   Signal transduction through NF-κB [J].
May, MJ ;
Ghosh, S .
IMMUNOLOGY TODAY, 1998, 19 (02) :80-88
[30]   A highly selective inhibitor of IκB kinase, BMS-345541, blocks both joint inflammation and destruction in collagen-induced arthritis in mice [J].
McIntyre, KW ;
Shuster, DJ ;
Gillooly, KM ;
Dambach, DM ;
Pattoli, MA ;
Lu, P ;
Zhou, XD ;
Qiu, YP ;
Zusi, FC ;
Burke, JR .
ARTHRITIS AND RHEUMATISM, 2003, 48 (09) :2652-2659