Norman Bryan H, McDermott Jeff S
Discovery Chemistry Research and Technologies and ‡Neurophysiology, Lilly Research Laboratories, A Division of Eli Lilly and Company , Indianapolis, Lilly Corporate Center, Indiana 46285, United States.
J Med Chem. 2017 Jan 12;60(1):66-88. doi: 10.1021/acs.jmedchem.6b00964. Epub 2016 Oct 25.
The neurotrophin nerve growth factor (NGF) has been implicated as a key mediator of chronic pain. NGF binds the tropomysin receptor kinase A (TrkA) and p75, resulting in the activation of downstream signaling pathways that have been linked to pro-nociception. While anti-NGF antibodies have demonstrated analgesia both preclinically and in patients, the mechanism of action of these agents remains unclear. We describe ligands targeting NGF, its receptors, and downstream/related targets. This Perspective highlights large and small molecule approaches to targeting the NGF-TrkA pathway both extra- and intracellularly. In addition, we present a strategic framework for future drug discovery efforts in this pathway beyond the targeting of NGF or its receptors. While existing tools have greatly informed NGF-mediated signaling, ongoing and future pathway research may help focus new drug discovery efforts on key novel targets and mechanisms. This may result in highly differentiated therapeutics with greater efficacy and/or improved safety profiles.
神经营养因子神经生长因子(NGF)被认为是慢性疼痛的关键介质。NGF与原肌球蛋白受体激酶A(TrkA)和p75结合,导致下游信号通路的激活,这些通路与伤害感受增强有关。虽然抗NGF抗体在临床前和患者中均已显示出镇痛作用,但其作用机制仍不清楚。我们描述了靶向NGF、其受体以及下游/相关靶点的配体。本观点重点介绍了在细胞外和细胞内靶向NGF-TrkA途径的大分子和小分子方法。此外,我们还提出了一个战略框架,用于该途径未来的药物发现工作,而不仅仅是靶向NGF或其受体。虽然现有工具为NGF介导的信号传导提供了很多信息,但正在进行和未来的途径研究可能有助于将新的药物发现工作集中在关键的新靶点和机制上。这可能会产生具有更高疗效和/或更好安全性的高度差异化疗法。