Department of Applied Biology, Kyoto Institute of Technology, Matsugasaki, Sakyo-ku, Kyoto, Japan.
J Antibiot (Tokyo). 2009 Dec;62(12):655-67. doi: 10.1038/ja.2009.98. Epub 2009 Oct 16.
Pro-inflammatory cytokines, such as tumor necrosis factor-alpha and interleukin-1, trigger the signal transduction pathway leading to the activation of the transcription factor, nuclear factor-kappaB (NF-kappaB). NF-kappaB induces a large number of target genes involved in many biological processes, such as inflammation, immunity, cell survival, cell death and carcinogenesis. As therapeutic agents for inflammatory diseases and cancer, as well as bioprobes for the characterization of intracellular biological response and cell function, a large number of natural and synthetic small molecules have been identified to inhibit the activation of the NF-kappaB signaling pathway. This review focuses on recent progress in the identification and biological properties of small molecules targeting the NF-kappaB signaling pathway induced by pro-inflammatory cytokines.
促炎细胞因子,如肿瘤坏死因子-α和白细胞介素-1,触发信号转导途径,导致转录因子核因子-κB(NF-κB)的激活。NF-κB 诱导大量参与许多生物学过程的靶基因,如炎症、免疫、细胞存活、细胞死亡和癌变。作为炎症性疾病和癌症的治疗剂,以及用于描述细胞内生物学反应和细胞功能的生物探针,已经鉴定出大量天然和合成的小分子来抑制 NF-κB 信号通路的激活。本综述重点介绍了最近在鉴定和研究针对促炎细胞因子诱导的 NF-κB 信号通路的小分子方面的进展。