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Ten Years and Counting: Moving Leucine-Rich Repeat Kinase 2 Inhibitors to the Clinic

机译:十年和计数:将富含亮氨酸的重复激酶2抑制剂移至临床

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摘要

The burden that Parkinson's disease (PD) exacts on the population continues to increase year after year. Though refinement of symptomatic treatments continues at a reasonable pace, no accepted therapies are available to slow or prevent disease progression. The leucine-rich repeat kinase 2 (LRRK2) gene was identified in PD genetic studies and offers new hope for novel therapeutic approaches. The evidence linking LRRK2 kinase activity to PD susceptibility is presented, as well as seminal discoveries relevant to the prosecution of LRRK2 kinase inhibition. Finally, suggestions are made for predictive preclinical modeling and successful first-in-human trials. © 2014 The Authors. Movement Disorders published by Wiley Periodicals, Inc. on behalf of International Parkinson and Movement Disorder Society.
机译:帕金森氏病(PD)对人口造成的负担逐年增加。尽管对症治疗的改进以合理的速度持续进行,但尚无公认的疗法可用于减缓或预防疾病的进展。 PD基因研究中鉴定出富含亮氨酸的重复激酶2(LRRK2)基因,为新型治疗方法提供了新希望。提供了将LRRK2激酶活性与PD易感性联系起来的证据,以及与起诉LRRK2激酶抑制作用有关的开创性发现。最后,为预测性临床前建模和成功的首次人体试验提出了建议。 ©2014作者。 Wiley Periodicals,Inc.代表国际帕金森病和运动障碍学会出版的《运动障碍》。

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