p21活化激酶为肥厚性心肌病提供了新的药物靶点

Yu He, Ming Lei
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摘要

何宇,雷明,*牛津大学药学系,Mansfield Road, Oxford, OX1 3QT, UK *通讯:ming.lei@pharm.ox.ac.uk收稿:2023年2月17日接受:2023年3月26日发表:2023年8月21日肥厚性心肌病(HCM)主要涉及肌瘤蛋白的突变,是最常见的遗传性心脏病,也是年轻人和运动员猝死的主要原因。HCM患者表现为心脏肥厚、纤维化和舒张功能障碍,通常呈进行性。尽管在了解HCM的分子遗传学基础方面取得了重大进展,但仍然缺乏有效和特异性的治疗方法来预防HCM的疾病进展。本文首先概述了HCM疾病进展的致病基础的最新进展,特别是钙处理功能障碍、线粒体损伤和内质网应激。本文分析了多功能酶p21活化激酶-1和激酶- 2 (Pak1/2)在心脏中的关键作用的证据,以及它们作为病理性肥厚和相关室性心律失常的有希望的药物靶点的治疗价值。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
p21-Activated Kinases Present a New Drug Target for Hypertrophic Cardiomyopathy
Expert review p21-Activated Kinases Present a New Drug Target for Hypertrophic Cardiomyopathy He Yu , and Lei Ming , * Department of Pharmacology, University of Oxford, Mansfield Road, Oxford, OX1 3QT, UK * Correspondence: ming.lei@pharm.ox.ac.uk Received: 17 February 2023 Accepted: 26 March 2023 Published: 21 August 2023 Abstract: Hypertrophic cardiomyopathy (HCM), primarily involving mutations in sarcomeric proteins, is the most common form of inherited heart disease and a leading cause of sudden death in young adults and athletes. HCM patients present with cardiac hypertrophy, fibrosis, and diastolic dysfunction often in a progressive manner. Despite significant progress made in understanding the molecular genetic basis of HCM, there remains a lack of effective and specific treatment for preventing disease progression in HCM. This article first provides an overview of recent progress in understanding the pathogenic basis of disease progression in HCM, in particular dysfunctional calcium handling, mitochondrial impairment, and endoplasmic reticulum stress. This article then analyses the evidence for critical roles of the multifunctional enzymes P21-activated kinase-1 and 2 (Pak1/2) in the heart and our opinion on their therapeutic value as a promising druggable target in pathological hypertrophy and associated ventricular arrhythmias.
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