Bamborough Paul, Callahan James F, Christopher John A, Kerns Jeffrey K, Liddle John, Miller David D, Morse Mary A, Rumsey William L, Williamson Rick
GlaxoSmithKline R&D, Medicines Research Centre, Gunnels Wood Road, Stevenage, Hertfordshire SG1 2NY, UK.
Curr Top Med Chem. 2009;9(7):623-39. doi: 10.2174/156802609789007336.
The IkappaB kinases (IKKs) are essential components of the signaling pathway by which the NF-kappaB p50/RelA transcription factor is activated in response to pro-inflammatory stimuli such as lipopolysaccharide (LPS) and tumor necrosis factor (TNFalpha). NF-kappaB signaling results in the expression of numerous genes involved in innate and adaptive immune responses. The pathway is also implicated in chronic inflammatory disorders including rheumatoid arthritis (RA), chronic obstructive pulmonary disorder (COPD), and asthma. Inhibition of the kinase activity of the IKKs is therefore a promising mechanism for intervention in these diseases. Here, we will review the literature describing small molecule inhibitors of IKKbeta (IKK2), the most widely studied of the IKKs.
IκB激酶(IKKs)是信号通路的重要组成部分,通过该通路,核因子κB p50/RelA转录因子在诸如脂多糖(LPS)和肿瘤坏死因子(TNFα)等促炎刺激下被激活。核因子κB信号传导导致众多参与先天性和适应性免疫反应的基因表达。该通路还与包括类风湿性关节炎(RA)、慢性阻塞性肺疾病(COPD)和哮喘在内的慢性炎症性疾病有关。因此,抑制IKKs的激酶活性是干预这些疾病的一种有前景的机制。在此,我们将综述描述IKKβ(IKK2)小分子抑制剂的文献,IKKβ是研究最为广泛的IKK。