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PCSK9: a convertase that coordinates LDL catabolism
Journal of Lipid Research · 2008 · Vol. 50 · pp. S172–S177
Jay D. Horton✉(Southwestern Medical Center)Jonathan C. Cohen(The University of Texas Southwestern Medical Center)Helen H. Hobbs✉(The University of Texas Southwestern Medical Center)
Abstract
The identification and characterization of proprotein convertase subtilisin-like/kexin type 9 (PCSK9) have provided new insights into LDL metabolism and the causal role of LDL in coronary heart disease (CHD). PCSK9 is a secreted protease that mediates degradation of the LDL receptor by interacting with the extracellular domain and targeting the receptor for degradation. Individuals with loss-of-function mutations in PCSK9 have reduced plasma levels of LDL cholesterol and are protected from CHD; these observations have validated PCSK9 as a therapeutic target and suggested new approaches for the treatment and prevention of CHD.
Lipoproteins and Cardiovascular HealthEnzyme Structure and FunctionPlant biochemistry and biosynthesisPCSK9Proprotein convertaseKexinLDL receptorSubtilisinCatabolismChemistryCholesterolInternal medicineEndocrinology
MeSH terms
AnimalsBiological TransportHumansCholesterol, LDLProtein BindingSerine EndopeptidasesSerine Proteinase InhibitorsApoptosis
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Nature Genetics · 2003 · 2,977 citations
The C679X mutation in PCSK9 is present and lowers blood cholesterol in a Southern African population
Atherosclerosis · 2006 · 363 citations
Comparison of the efficacy and safety of rosuvastatin versus atorvastatin, simvastatin, and pravastatin across doses (STELLAR**STELLAR = Statin Therapies for Elevated Lipid Levels compared Across doses to Rosuvastatin. Trial)
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