State Key Laboratory of Quality Research in Chinese Medicine, Institute of Chinese Medical Sciences, University of Macau, Macao 999078, China.
Department of Chemistry, Hong Kong Baptist University, Kowloon Tong, Hong Kong 999077, China.
Int J Mol Sci. 2019 Sep 10;20(18):4445. doi: 10.3390/ijms20184445.
Due to role of the Keap1-Nrf2 protein-protein interaction (PPI) in protecting cells from oxidative stress, the development of small molecule inhibitors that inhibit this interaction has arisen as a viable approach to combat maladies caused by oxidative stress, such as cancers, neurodegenerative disease and diabetes. To obtain specific and genuine Keap1-Nrf2 inhibitors, many efforts have been made towards developing new screening approaches. However, there is no inhibitor for this target entering the clinic for the treatment of human diseases. New strategies to identify novel bioactive compounds from large molecular databases and accelerate the developmental process of the clinical application of Keap1-Nrf2 protein-protein interaction inhibitors are greatly needed. In this review, we have summarized virtual screening and other methods for discovering new lead compounds against the Keap1-Nrf2 protein-protein interaction. We also discuss the advantages and limitations of different strategies, and the potential of this PPI as a drug target in disease therapy.
由于 Keap1-Nrf2 蛋白-蛋白相互作用(PPI)在保护细胞免受氧化应激方面的作用,开发抑制这种相互作用的小分子抑制剂已成为一种可行的方法,可用于治疗由氧化应激引起的疾病,如癌症、神经退行性疾病和糖尿病。为了获得特异性和真正的 Keap1-Nrf2 抑制剂,人们已经做出了许多努力来开发新的筛选方法。然而,目前还没有针对这一靶点的抑制剂用于治疗人类疾病。因此,非常需要新的策略来从大型分子数据库中识别新型生物活性化合物,并加速 Keap1-Nrf2 蛋白-蛋白相互作用抑制剂的临床应用开发过程。在这篇综述中,我们总结了针对 Keap1-Nrf2 蛋白-蛋白相互作用的新型先导化合物的虚拟筛选和其他发现方法。我们还讨论了不同策略的优缺点,以及该 PPI 在疾病治疗中的作为药物靶点的潜力。