p38 map kinases: Key signalling molecules as therapeutic targets for inflammatory diseases

被引:1041
作者
Kumar, S [1 ]
Boehm, J [1 ]
Lee, JC [1 ]
机构
[1] GlaxoSmithKline, Pharmaceut Res & Dev, King Of Prussia, PA 19406 USA
关键词
D O I
10.1038/nrd1177
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
The p38 MAP kinases are a family of serine/threonine protein kinases that play important roles in cellular responses to external stress signals. Since their identification about 10 years ago, much has been learned of the activation and regulation of the p38 MAP kinase pathways. Inhibitors of two members of the p38 family have been shown to have anti-inflammatory effects in preclinical disease models, primarily through the inhibition of the expression of inflammatory mediators. Several promising compounds have also progressed to clinical trials. In this review, we provide an overview of the role of p38 MAP kinases in stress-activated pathways and the progress towards clinical development of p38 MAP kinase inhibitors in the treatment of inflammatory diseases.
引用
收藏
页码:717 / 726
页数:10
相关论文
共 77 条
  • [21] Suppression of the clinical and cytokine response to endotoxin by RWJ-67657, a p38 mitogen-activated protein-kinase inhibitor, in healthy human volunteers
    Fijen, JW
    Zijlstra, JG
    De Boer, P
    Spanjersberg, R
    Tervaert, JWC
    Van der Werf, TS
    Ligtenberg, JJM
    Tulleken, JE
    [J]. CLINICAL AND EXPERIMENTAL IMMUNOLOGY, 2001, 124 (01) : 16 - 20
  • [22] A single amino acid substitution makes ERK2 susceptible to pyridinyl imidazole inhibitors of p38 MAP kinase
    Fox, T
    Coll, JT
    Xie, XL
    Ford, PJ
    Germann, UA
    Porter, MD
    Pazhanisamy, S
    Fleming, MA
    Galullo, V
    Su, MSS
    Wilson, KP
    [J]. PROTEIN SCIENCE, 1998, 7 (11) : 2249 - 2255
  • [23] p38 mitogen-activated protein kinase-dependent and -independent signaling of mRNA stability of AU-rich element-containing transcripts
    Frevel, MAE
    Bakheet, T
    Silva, AM
    Hissong, JG
    Khabar, KSA
    Williams, BRG
    [J]. MOLECULAR AND CELLULAR BIOLOGY, 2003, 23 (02) : 425 - 436
  • [24] Fullerton T, 2000, CLIN PHARMACOL THER, V67, P114
  • [25] Regulation of stress-induced cytokine production by pyridinylimidazoles; Inhibition of CSBP kinase
    Gallagher, TF
    Seibel, GL
    Kassis, S
    Laydon, JT
    Blumenthal, MJ
    Lee, JC
    Lee, D
    Boehm, JC
    FierThompson, SM
    Abt, JW
    Soreson, ME
    Smietana, JM
    Hall, RF
    Garigipati, RS
    Bender, PE
    Erhard, KF
    Krog, AJ
    Hofmann, GA
    Sheldrake, PL
    McDonnell, PC
    Kumar, S
    Young, PR
    Adams, JL
    [J]. BIOORGANIC & MEDICINAL CHEMISTRY, 1997, 5 (01) : 49 - 64
  • [26] 2,4,5-TRIARYLIMIDAZOLE INHIBITORS OF IL-1 BIOSYNTHESIS
    GALLAGHER, TF
    FIERTHOMPSON, SM
    GARIGIPATI, RS
    SORENSON, ME
    SMIETANA, JM
    LEE, D
    BENDER, PE
    LEE, JC
    LAYDON, JT
    GRISWOLD, DE
    CHABOTFLETCHER, MC
    BRETON, JJ
    ADAMS, JL
    [J]. BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, 1995, 5 (11) : 1171 - 1176
  • [27] MAPKK-independent activation of p38α mediated by TAB1-dependent autophosphorylation of p38α
    Ge, BX
    Gram, H
    Di Padova, F
    Huang, B
    New, L
    Ulevitch, RJ
    Luo, Y
    Han, JH
    [J]. SCIENCE, 2002, 295 (5558) : 1291 - 1294
  • [28] GOLDSTEIN DM, 2002, J INFLAMM RES, V51, pS114
  • [29] Induction of cyclooxygenase-2 by the activated MEKK1→SEK1/MKK4→p38 mitogen-activated protein kinase pathway
    Guan, ZH
    Buckman, SY
    Pentland, AP
    Templeton, DJ
    Morrison, AR
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (21) : 12901 - 12908
  • [30] Acquisition of sensitivity of stress-activated protein kinases to the p38 inhibitor, SB 203580, by alteration of one or more amino acids within the ATP binding pocket
    Gum, RJ
    McLaughlin, MM
    Kumar, S
    Wang, ZL
    Bower, MJ
    Lee, JC
    Adams, JL
    Livi, GP
    Goldsmith, EJ
    Young, PR
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (25) : 15605 - 15610