RSK3 Anchoring Disruptor Therapy for Heart Failure

RSK3 锚定破坏器治疗心力衰竭

基本信息

批准号：
8977557
负责人：
Michael Seth Kapiloff
金额：
$ 29.9万
依托单位：
ANCHORED RSK3 INHIBITORS, LLC
依托单位国家：
美国
项目类别：
财政年份：
2015
资助国家：
美国
起止时间：
2015-08-01 至 2016-07-31
项目状态：
已结题

来源：
https://reporter.nih.gov/project-details/8977557
关键词：
3-Phosphoinositide Dependent Protein Kinase-1 A kinase anchoring protein Affinity American Animal Model Animals Aortic Valve Stenosis Apoptosis Attenuated Binding Biological Products Cardiac Cardiac Myocytes Cardiovascular Diseases Cause of Death Cell Nucleus Cessation of life Cicatrix Clinical Coronary Arteriosclerosis Coronary artery Cytosol Data Dependovirus Development Diagnosis Disease Enzymes Etiology Family Fibrosis Functional disorder Future Gene Expression Gene Transduction Agent Genetic Models Goals Grant Growth Heart Heart failure Hypertension Hypertrophy In Vitro Infarction Infusion procedures Investigational New Drug Application Knock-out Left Ligation MEKKs MEKs Modeling Mus Muscle Muscle Cells Myocardial Myocardial Infarction N-terminal Nuclear Pathology Pathway interactions Patients Peptides Phase Phosphatidylinositols Phosphorylation Phosphotransferases Play Prevention Protein Isoforms Protein Kinase Quality of life RPS6KA gene Regulation Research Ribosomal Protein S6 Kinase Role Scaffolding Protein Signal Pathway Signal Transduction Small Business Technology Transfer Research Specificity Stress Syndrome Tertiary Protein Structure Testing Therapeutic base commercialization common treatment constriction improved in vivo inhibitor/antagonist insight interstitial member mortality novel novel therapeutic intervention novel therapeutics patient population pressure prevent protein protein interaction public health relevance response scaffold selective expression

项目摘要

DESCRIPTION (provided by applicant): Pathological cardiac remodeling, including myocyte hypertrophy and apoptosis and myocardial interstitial fibrosis, constitutes a common pathway to heart failure in disease. Despite current pharmacologic therapy and other advances that attenuate remodeling, mortality due to heart failure remains high. New, more effective therapeutic options are desperately needed in an increasing patient population to improve both the survival and quality of life for patients with or susceptible to heart failure. We recently discovered that the protein kinase p90 ribosomal S6 kinase type 3 (RSK3) plays a critical role in the regulation of pathological cardiac remodeling. In 2013, Anchored RSK3 Inhibitors, LLC, was founded by Dr. Michael Kapiloff to develop novel therapeutics based upon RSK3 inhibition that will prevent and/or treat heart failure. RSK3 was required for pathological remodeling even though RSK3 is less abundant in the cardiac myocyte than other members of the RSK protein kinase family. We found that in myocytes RSK3's unique N- terminal domain conferred high affinity, regulated binding to the scaffold protein muscle A-kinase anchoring protein (mAKAPß). This novel protein-protein interaction explained the selective binding of that kinase isoform to the scaffold. New preliminary data show that expression both in vitro and in vivo of an anchoring disruptor peptide that blocks mAKAPß-RSK3 binding will attenuate pathological remodeling, preventing the development of heart failure in response to pressure overload. The goal of this STTR application is to support the development of a new adeno-associated virus (AAV) gene therapy vector that expresses the RSK3 anchoring disruptor peptide. The proposed research will provide proof-of-concept for a new therapeutic approach for the treatment and/or prevention of heart failure based upon RSK3 displacement within the myocyte. SPECIFIC AIM 1: Treatment of Pressure Overload-induced Heart Failure by Anchoring Disruptor Therapy. Cardiac myocyte-selective expression of a mAKAPß RSK3-binding peptide (RBD) using AAV prevents transverse aortic constriction-induced heart failure in vivo. In this Aim we will test whether RSK3 anchoring disruptor therapy can induce reverse remodeling and treat heart failure in mice with established pathology due to pressure overload. SPECIFIC AIM 2: Prevention of Myocardial Infarction-induced Heart Failure by Anchoring Disruptor Therapy. In this Aim, we will test whether AAV-RBD can block remodeling following myocardial infarction without having deleterious effects on infarct size or scar formation. Results obtained through this phase I STTR grant will provide insight into how broadly AAV-RBD therapy may be applied in cardiovascular disease and inform the choice of subsequent large animal studies necessary to progress to a FDA Investigational New Drug Application.

描述（由申请人提供）：病理性心脏重塑，包括心肌细胞肥大和细胞凋亡以及心肌间质纤维化，构成了疾病中心力衰竭的常见途径，尽管目前的药物治疗和其他进展减轻了重塑，但心力衰竭引起的死亡率仍然很高。越来越多的患者群体迫切需要新的、更有效的治疗方案，以改善患有或易患心力衰竭的患者的生存和生活质量。我们最近发现蛋白激酶 p90。核糖体 S6 激酶 3 型 (RSK3) 在病理性心脏重塑的调节中发挥着关键作用。 Michael Kapiloff 博士于 2013 年创立了 Anchored RSK3 Inhibitors, LLC，旨在开发基于 RSK3 抑制的新型疗法，以预防和/或抑制心脏重塑。尽管我们发现心肌细胞中的 RSK3 含量低于 RSK 蛋白激酶家族的其他成员，但 RSK3 是治疗心力衰竭所必需的。 RSK3 独特的 N 端结构域赋予支架蛋白肌肉 A 激酶锚定蛋白 (mAKAPß) 的高亲和力、受调节的结合，这种新颖的蛋白质-蛋白质相互作用解释了该激酶亚型与支架的选择性结合。在体外和体内，阻断 mAKAPß-RSK3 结合的锚定干扰肽将减弱病理重塑，防止因压力超负荷而发生心力衰竭。 STTR 应用旨在支持开发表达 RSK3 锚定破坏肽的新型腺相关病毒 (AAV) 基因治疗载体。拟议的研究将为治疗和/或预防的新治疗方法提供概念验证。基于心肌细胞内 RSK3 位移的心力衰竭具体目标 1：通过锚定干扰素疗法治疗心肌细胞选择性表达 mAKAPß。使用 AAV 的 RSK3 结合肽 (RBD) 可在体内预防横向主动脉缩窄引起的心力衰竭。在本目标中，我们将测试 RSK3 锚定干扰物疗法是否可以诱导逆转重塑并治疗因压力超负荷而导致的病理学小鼠的心力衰竭。目标 2：通过锚定破坏疗法预防心肌梗塞引起的心力衰竭在这个目标中，我们将测试 AAV-RBD 是否可以阻断以下重构。心肌梗塞，而不会对梗塞面积或疤痕形成产生有害影响。第一阶段 STTR 资助将深入了解 AAV-RBD 疗法在心血管疾病中的应用范围，并为后续大动物研究的选择提供信息，以推进 FDA 新药研究申请。