Target intelligence / Profile preview

Hepatic Triglyceride Lipase (HTGL)

Target
HTGL
Molecular classification
Enzyme, AB hydrolase superfamily
01

Overview

Hepatic triglyceride lipase (HTGL), also known as hepatic lipase (HL) or LIPC, is a key enzyme in lipid metabolism. It catalyzes the hydrolysis of triglycerides, phospholipids, mono-, di-glycerides, and acyl-CoA thioesters present in circulating plasma lipoproteins. HTGL plays an essential role in regulating plasma levels of intermediate-density lipoprotein (IDL), low-density lipoprotein (LDL), very low–density lipoproteins (VLDLs), chylomicron remnants, HDL cholesterol, and phospholipids. Deficiency or mutations in LIPC/HTGL can lead to hepatic lipase deficiency—a disorder characterized by elevated beta-migrating VLDLs and abnormally triglyceride-rich LDLs/HDLs. This may manifest clinically as hypercholesterolemia or hypertriglyceridemia with increased risk for coronary artery disease due to altered lipid profiles.

Other names
HLLIPC
02

Mechanism of action

Inhibition of triglyceride hydrolysis in lipoproteins, modulation of lipoprotein particle size and composition.

03

Biological functions

Lipid hydrolysisLipoprotein remodelingReceptor-mediated uptakeTriacylglycerol hydrolase activityPhospholipase activityCholesterol metabolic processReverse cholesterol transportTriacylglycerol catabolic processFatty acid biosynthetic process
04

Disease associations

Cardiovascular diseaseDyslipidemiaHypercholesterolemiaHypertriglyceridemia
05

Safety considerations

Potential impact on HDL metabolismOff-target effects on other lipases
06

Biomarkers

HTGL activity levels in plasmaLIPC gene mutations

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