Your browser doesn't support javascript.
loading
Protein kinase C mechanisms that contribute to cardiac remodelling.
Newton, Alexandra C; Antal, Corina E; Steinberg, Susan F.
Afiliação
  • Newton AC; Department of Pharmacology, University of California at San Diego, La Jolla, CA 92093, U.S.A. sfs1@columbia.edu anewton@ucsd.edu.
  • Antal CE; Department of Pharmacology, University of California at San Diego, La Jolla, CA 92093, U.S.A. Biomedical Sciences Graduate Program, University of California at San Diego, La Jolla, CA 92093, U.S.A.
  • Steinberg SF; Department of Pharmacology, Columbia University, New York, NY 10032, U.S.A. sfs1@columbia.edu anewton@ucsd.edu.
Clin Sci (Lond) ; 130(17): 1499-510, 2016 09 01.
Article em En | MEDLINE | ID: mdl-27433023
ABSTRACT
Protein phosphorylation is a highly-regulated and reversible process that is precisely controlled by the actions of protein kinases and protein phosphatases. Factors that tip the balance of protein phosphorylation lead to changes in a wide range of cellular responses, including cell proliferation, differentiation and survival. The protein kinase C (PKC) family of serine/threonine kinases sits at nodal points in many signal transduction pathways; PKC enzymes have been the focus of considerable attention since they contribute to both normal physiological responses as well as maladaptive pathological responses that drive a wide range of clinical disorders. This review provides a background on the mechanisms that regulate individual PKC isoenzymes followed by a discussion of recent insights into their role in the pathogenesis of diseases such as cancer. We then provide an overview on the role of individual PKC isoenzymes in the regulation of cardiac contractility and pathophysiological growth responses, with a focus on the PKC-dependent mechanisms that regulate pump function and/or contribute to the pathogenesis of heart failure.
Assuntos
Palavras-chave

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Proteína Quinase C / Coração / Miocárdio Limite: Animals / Humans Idioma: En Revista: Clin Sci (Lond) Ano de publicação: 2016 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Proteína Quinase C / Coração / Miocárdio Limite: Animals / Humans Idioma: En Revista: Clin Sci (Lond) Ano de publicação: 2016 Tipo de documento: Article