Chan Sharon L, Tan Eng-King
a Department of Neurology , National Neuroscience institute, Duke NUS Medical School , Singapore.
Expert Opin Ther Targets. 2017 Jun;21(6):601-610. doi: 10.1080/14728222.2017.1323881. Epub 2017 May 15.
LRRK2 research has progressed significantly in recent years with more reports of LRRK2 interactors and the development of more specific and sophisticated LRRK2 kinase inhibitors. Identification of bone fide LRRK2 substrates will provide new therapeutic targets in LRRK2-linked Parkinson's disease (PD). Areas covered: This review aims to put current LRRK2 research into perspective. Beginning with recent LRRK2 mammalian models employed for in vivo validation of LRRK2 substrates, followed by updates on reported LRRK2 interactors and their inferred mechanisms. Finally an overview of commonly used LRRK2 kinase inhibitors will be depicted. Expert opinion: Identification of LRRK2 non-kinase functions suggests the possibility of alternative LRRK2 drug target sites and these should be further explored. Studies on the effects of LRRK2 kinase inhibition on its non-kinase function and its self-regulatory role will provide further insights on its pathophysiologic mechanisms. Development of robust measurements of LRRK2 inhibitor efficacy will be required. These would include identification of specific imaging ligands or direct biochemical assays that can accurately capture its intrinsic activity. Testing of new therapeutic drug targets in both LRRK2 carriers and non LRRK2-linked patients will be important since their phenotype is similar.
近年来,随着更多关于LRRK2相互作用蛋白的报道以及更特异、更复杂的LRRK2激酶抑制剂的研发,LRRK2研究取得了显著进展。确定真正的LRRK2底物将为LRRK2相关帕金森病(PD)提供新的治疗靶点。涵盖领域:本综述旨在全面介绍当前的LRRK2研究。首先介绍最近用于体内验证LRRK2底物的LRRK2哺乳动物模型,接着是关于已报道的LRRK2相互作用蛋白及其推测机制的最新情况。最后将概述常用的LRRK2激酶抑制剂。专家观点:LRRK2非激酶功能的确定提示了替代LRRK2药物靶点的可能性,应进一步探索。关于LRRK2激酶抑制对其非激酶功能及其自我调节作用影响的研究将为其病理生理机制提供进一步的见解。需要开发可靠的LRRK2抑制剂疗效测量方法。这将包括鉴定能够准确捕捉其内在活性的特异性成像配体或直接生化检测方法。在LRRK2携带者和非LRRK2相关患者中测试新的治疗药物靶点将很重要,因为他们的表型相似。