CaMKII as a Therapeutic Target in Cardiovascular Disease

Author:

Reyes Gaido Oscar E.1,Nkashama Lubika J.2,Schole Kate L.1,Wang Qinchuan1,Umapathi Priya1,Mesubi Olurotimi O.1,Konstantinidis Klitos1,Luczak Elizabeth D.1,Anderson Mark E.13

Affiliation:

1. Department of Medicine, The Johns Hopkins University School of Medicine, Baltimore, Maryland, USA;

2. Cleveland Clinic Lerner College of Medicine, Cleveland, Ohio, USA

3. Departments of Physiology and Genetic Medicine and Program in Cellular and Molecular Medicine, The Johns Hopkins University School of Medicine, Baltimore, Maryland, USA

Abstract

CaMKII (the multifunctional Ca2+ and calmodulin-dependent protein kinase II) is a highly validated signal for promoting a variety of common diseases, particularly in the cardiovascular system. Despite substantial amounts of convincing preclinical data, CaMKII inhibitors have yet to emerge in clinical practice. Therapeutic inhibition is challenged by the diversity of CaMKII isoforms and splice variants and by physiological CaMKII activity that contributes to learning and memory. Thus, uncoupling the harmful and beneficial aspects of CaMKII will be paramount to developing effective therapies. In the last decade, several targeting strategies have emerged, including small molecules, peptides, and nucleotides, which hold promise in discriminating pathological from physiological CaMKII activity. Here we review the cellular and molecular biology of CaMKII, discuss its role in physiological and pathological signaling, and consider new findings and approaches for developing CaMKII therapeutics.

Publisher

Annual Reviews

Subject

Pharmacology,Toxicology

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