Department of Biology, Swiss Federal Institute of Technology (ETH) Zurich, 8093 Zurich, Switzerland.
J Biol Chem. 2012 Sep 21;287(39):33001-13. doi: 10.1074/jbc.M112.383430. Epub 2012 Jul 31.
Nuclear factor erythroid-derived 2-related factor 2 (Nrf2) is a master regulator of cellular antioxidant defense systems, and activation of this transcription factor is a promising strategy for protection of skin and other organs from environmental insults. To identify efficient Nrf2 activators in keratinocytes, we combined a chemical library screen with computer-based virtual screening. Among 14 novel Nrf2 activators, the most potent compound, a nitrophenyl derivative of 2-chloro-5-nitro-N-phenyl-benzamide, was characterized with regard to its molecular mechanism of action. This compound induced the expression of cytoprotective genes in keratinocytes isolated from wild-type but not from Nrf2-deficient mice. Most importantly, it showed low toxicity and protected primary human keratinocytes from UVB-induced cell death. Therefore, it represents a potential lead compound for the development of drugs for skin protection under stress conditions. Our study demonstrates that chemical library screening combined with advanced computational similarity searching is a powerful strategy for identification of bioactive compounds, and it points toward an innovative therapeutic approach against UVB-induced skin damage.
核因子红细胞 2 相关因子 2(Nrf2)是细胞抗氧化防御系统的主要调节因子,激活该转录因子是保护皮肤和其他器官免受环境损伤的一种有前途的策略。为了在角质细胞中鉴定有效的 Nrf2 激活剂,我们将化学文库筛选与基于计算机的虚拟筛选相结合。在 14 种新型 Nrf2 激活剂中,最有效的化合物是 2-氯-5-硝基-N-苯基苯甲酰胺的硝基苯基衍生物,其作用机制已得到表征。该化合物诱导了来自野生型而非 Nrf2 缺陷型小鼠的角质细胞中保护性基因的表达。最重要的是,它表现出低毒性,并能保护原代人角质细胞免受 UVB 诱导的细胞死亡。因此,它代表了一种用于在应激条件下保护皮肤的药物开发的潜在先导化合物。我们的研究表明,化学文库筛选与先进的计算相似性搜索相结合是鉴定生物活性化合物的强大策略,并指出了一种针对 UVB 诱导的皮肤损伤的创新治疗方法。