Willems Sabine, Zaienne Daniel, Merk Daniel
Institute of Pharmaceutical Chemistry, Goethe University Frankfurt, Max-von-Laue-Strasse 9, 60438 Frankfurt, Germany.
J Med Chem. 2021 Jul 22;64(14):9592-9638. doi: 10.1021/acs.jmedchem.1c00186. Epub 2021 Jul 12.
Nuclear receptors, also known as ligand-activated transcription factors, regulate gene expression upon ligand signals and present as attractive therapeutic targets especially in chronic diseases. Despite the therapeutic relevance of some nuclear receptors in various pathologies, their potential in neurodegeneration and neuroinflammation is insufficiently established. This perspective gathers preclinical and clinical data for a potential role of individual nuclear receptors as future targets in Alzheimer's disease, Parkinson's disease, and multiple sclerosis, and concomitantly evaluates the level of medicinal chemistry targeting these proteins. Considerable evidence suggests the high promise of ligand-activated transcription factors to counteract neurodegenerative diseases with a particularly high potential of several orphan nuclear receptors. However, potent tools are lacking for orphan receptors, and limited central nervous system exposure or insufficient selectivity also compromises the suitability of well-studied nuclear receptor ligands for functional studies. Medicinal chemistry efforts are needed to develop dedicated high-quality tool compounds for the therapeutic validation of nuclear receptors in neurodegenerative pathologies.
核受体,也被称为配体激活转录因子,在配体信号作用下调节基因表达,是极具吸引力的治疗靶点,尤其是在慢性疾病方面。尽管某些核受体在多种病理状况下具有治疗相关性,但其在神经退行性变和神经炎症中的潜力尚未得到充分证实。本文综述了临床前和临床数据,探讨了个体核受体作为阿尔茨海默病、帕金森病和多发性硬化症未来治疗靶点的潜在作用,并同时评估了针对这些蛋白质的药物化学水平。大量证据表明,配体激活转录因子在对抗神经退行性疾病方面具有很高的前景,尤其是几种孤儿核受体具有特别高的潜力。然而,针对孤儿受体缺乏有效的工具,而且中枢神经系统暴露有限或选择性不足也影响了经过充分研究的核受体配体用于功能研究的适用性。需要开展药物化学研究,以开发专门的高质量工具化合物,用于在神经退行性疾病中对核受体进行治疗验证。