CaMKII as a Therapeutic Target in Cardiovascular Disease

Oscar E. Reyes Gaido, Lubika J. Nkashama, Kate L. Schole, Qinchuan Wang, Priya Umapathi, Olurotimi O. Mesubi, Klitos Konstantinidis, Elizabeth D. Luczak, Mark E. Anderson

Research output: Contribution to journalReview articlepeer-review

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.

Original languageEnglish (US)
Pages (from-to)249-272
Number of pages24
JournalAnnual Review of Pharmacology and Toxicology
Volume63
DOIs
StatePublished - Jan 20 2023

Keywords

  • CaMKII
  • arrhythmias
  • calcium
  • cardiovascular disease
  • heart failure
  • kinase

ASJC Scopus subject areas

  • Toxicology
  • Pharmacology

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