Disarm Therapeutics, One Main Street, 11th Floor, Cambridge, MA 02139, USA.
Disarm Therapeutics, One Main Street, 11th Floor, Cambridge, MA 02139, USA.
Trends Pharmacol Sci. 2020 Apr;41(4):281-293. doi: 10.1016/j.tips.2020.01.006. Epub 2020 Feb 24.
Attempts to develop neuroprotective treatments for neurodegenerative disorders have not yet been clinically successful. Axonal degeneration has been recognized as a predominant driver of disability and disease progression in central nervous system (CNS) diseases such as amyotrophic lateral sclerosis (ALS), multiple sclerosis, and Parkinson's disease, peripheral nervous system (PNS) disorders such as chemotherapy-induced, diabetic, and inherited neuropathies, and ocular disorders, such as glaucoma. In recent years, sterile alpha and TIR motif containing 1 (SARM1) has emerged as the first compelling axonal-specific target for therapeutic intervention. In this review, we discuss the role of axonal degeneration in neurodegenerative disorders, with a focus on SARM1 and the discovery of its intrinsic enzymatic function. Establishment of neurofilament light chain (NfL) as a reliable biomarker of axonal damage, and the availability of an ultrasensitive method for measuring NfL in plasma or serum, provide translational tools to make development of axonal protective, SARM1 inhibitors a viable approach to treat multiple neurodegenerative disorders.
尽管尝试开发神经保护疗法来治疗神经退行性疾病,但尚未在临床上取得成功。轴突变性已被认为是中枢神经系统(CNS)疾病(如肌萎缩侧索硬化症、多发性硬化症和帕金森病)、周围神经系统(PNS)疾病(如化疗诱导的、糖尿病和遗传性神经病以及眼部疾病,如青光眼)的残疾和疾病进展的主要驱动因素。近年来,无菌α和 TIR 基序包含 1(SARM1)已成为治疗干预的第一个强制性轴突特异性靶标。在这篇综述中,我们讨论了轴突变性在神经退行性疾病中的作用,重点介绍了 SARM1 及其内在酶功能的发现。神经丝轻链(NfL)作为轴突损伤可靠生物标志物的确立,以及在血浆或血清中测量 NfL 的超灵敏方法的可用性,为开发轴突保护 SARM1 抑制剂提供了转化工具,使其成为治疗多种神经退行性疾病的可行方法。