4.5 Review

Heat Shock Protein-60 and Risk for Cardiovascular Disease

Journal

CURRENT PHARMACEUTICAL DESIGN
Volume 17, Issue 33, Pages 3662-3668

Publisher

BENTHAM SCIENCE PUBL LTD
DOI: 10.2174/138161211798220981

Keywords

Chaperonin; heat shock protein 60; cardiomyocytes; heart failure; cardiovascular disease; atherosclerosis

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Cardiovascular disease (CVD) is a leading cause of morbidity and mortality worldwide. There is growing evidence that molecular chaperones, many of which are heat shock proteins HSPs, are involved in CVD pathogenesis. In this review we focus on HSP60, the human mitochondrial chaperone that also displays extramitochondrial and extracellular functions. HSP60 is typically cytoprotective but a number of stress conditions determine its conversion to a potentially toxic molecule for cells and tissues. We present illustrative examples of specific subtypes of CVD where HSP60 is implicated in the initiation and/or progression of disease. The data not only indicate a pathogenic role for HSP60 but also its potential as a biomarker with applications for diagnosis, assessing prognosis and response to treatment, as well as for preventing and treating CVD.

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