Prescott Jack A, Cook Simon J
Signalling Laboratory, The Babraham Institute, Babraham Research Campus, Cambridge CB22 3AT, UK.
Cells. 2018 Aug 23;7(9):115. doi: 10.3390/cells7090115.
Deregulated NF-κB signalling is implicated in the pathogenesis of numerous human inflammatory disorders and malignancies. Consequently, the NF-κB pathway has attracted attention as an attractive therapeutic target for drug discovery. As the primary, druggable mediator of canonical NF-κB signalling the IKKβ protein kinase has been the historical focus of drug development pipelines. Thousands of compounds with activity against IKKβ have been characterised, with many demonstrating promising efficacy in pre-clinical models of cancer and inflammatory disease. However, severe on-target toxicities and other safety concerns associated with systemic IKKβ inhibition have thus far prevented the clinical approval of any IKKβ inhibitors. This review will discuss the potential reasons for the lack of clinical success of IKKβ inhibitors to date, the challenges associated with their therapeutic use, realistic opportunities for their future utilisation, and the alternative strategies to inhibit NF-κB signalling that may overcome some of the limitations associated with IKKβ inhibition.
NF-κB信号通路失调与多种人类炎症性疾病和恶性肿瘤的发病机制有关。因此,NF-κB通路作为药物研发中一个有吸引力的治疗靶点备受关注。作为经典NF-κB信号通路的主要可药物化调节因子,IKKβ蛋白激酶一直是药物研发管线的历史焦点。数千种具有抗IKKβ活性的化合物已被鉴定,其中许多在癌症和炎症性疾病的临床前模型中显示出有前景的疗效。然而,与全身性IKKβ抑制相关的严重靶点毒性和其他安全问题迄今为止阻碍了任何IKKβ抑制剂的临床批准。本综述将讨论迄今为止IKKβ抑制剂临床应用未成功的潜在原因、其治疗应用相关的挑战、其未来应用的现实机会,以及抑制NF-κB信号通路的替代策略,这些策略可能克服与IKKβ抑制相关的一些局限性。