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

被引:1039
|
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 50 条
  • [41] p38 MAPK as a potential therapeutic target for inflammatory osteolysis
    Wei, Shi
    Siegal, Gene P.
    ADVANCES IN ANATOMIC PATHOLOGY, 2007, 14 (01) : 42 - 45
  • [42] Radiobrominated probe targeting activated p38α in inflammatory diseases
    Tomoyuki Hashimoto
    Naoya Kondo
    Akira Makino
    Yasushi Kiyono
    Takashi Temma
    Annals of Nuclear Medicine, 2022, 36 : 845 - 852
  • [43] Radiobrominated probe targeting activated p38α in inflammatory diseases
    Hashimoto, Tomoyuki
    Kondo, Naoya
    Makino, Akira
    Kiyono, Yasushi
    Temma, Takashi
    ANNALS OF NUCLEAR MEDICINE, 2022, 36 (10) : 845 - 852
  • [44] The p38 MAPK inhibitors for the treatment of inflammatory diseases and cancer
    Yong, Hae-Young
    Koh, Min-Soo
    Moon, Aree
    EXPERT OPINION ON INVESTIGATIONAL DRUGS, 2009, 18 (12) : 1893 - 1905
  • [45] Pro-Inflammatory Angiogenesis Is Mediated by p38 MAP Kinase
    Rajashekhar, Gangaraju
    Kamocka, Malgorzata
    Marin, Abby
    Suckow, Mark A.
    Wolter, William R.
    Badve, Sunil
    Sanjeevaiah, Aravind Raj
    Pumiglia, Kevin
    Rosen, Elliot
    Clauss, Matthias
    JOURNAL OF CELLULAR PHYSIOLOGY, 2011, 226 (03) : 800 - 808
  • [46] p38γ and p38δ: From Spectators to Key Physiological Players
    Cuenda, Ana
    Jose Sanz-Ezquerro, Juan
    TRENDS IN BIOCHEMICAL SCIENCES, 2017, 42 (06) : 431 - 442
  • [47] Targeting the p38α pathway in chronic inflammatory diseases: Could activation, not inhibition, be the appropriate therapeutic strategy?
    Heng, C. K. Matthew
    Gilad, Nechama
    Darlyuk-Saadon, Ilona
    Wong, W. S. Fred
    Engelberg, David
    PHARMACOLOGY & THERAPEUTICS, 2022, 235
  • [48] DUX4 expression activates JNK and p38 MAP kinases in myoblasts
    Brennan, Christopher M.
    Hill, Abby S.
    St Andre, Michael
    Li, Xianfeng
    Madeti, Vijaya
    Breitkopf, Susanne
    Garren, Seth
    Xue, Liang
    Gilbert, Tamara
    Hadjipanayis, Angela
    Monetti, Mara
    Emerson Jr, Charles P.
    Moccia, Robert
    Owens, Jane
    Christoforou, Nicolas
    DISEASE MODELS & MECHANISMS, 2022, 15 (11)
  • [49] Role of p38 MAP kinases in pressure-overload induced cardiac hypertrophy
    Hoshijima, M
    Gu, Y
    Li, MX
    Ross, J
    Chien, KR
    Wang, YB
    CIRCULATION, 2001, 104 (17) : 85 - 85
  • [50] Opposing effects of GMF on ERK and p38 map kinases during neuronal apoptosis
    Lim, R
    Zaheer, A
    FASEB JOURNAL, 1996, 10 (06): : 521 - 521