Inhibition of hepatic (V)LDL production by a novel antagonist of carboxyl esterase 1

NIH RePORTER · NIH · R01 · $512,957 · view on reporter.nih.gov ↗

Abstract

Project Summary We used a human iPSC-derived hepatocyte platform to identify a family of structurally related small molecules that can reduce the production of APOB by the liver. These small molecules are highly effective, do not cause abnormal lipid accumulation, and have a chemical structure that is distinct from any known cholesterol lowering drug. Such compounds have the potential to treat hypercholesterolemia and steatosis. In the current application we propose to define the molecular mechanisms through which the compounds act. In preliminary data we show that the compounds inhibit human carboxylesterase 1 (CES1). In the three proposed aims we will i) identify the binding characteristics of the compounds to CES1 and define their specificity using crystallography and biochemical assays, ii) use iPSC-hepatocytes to definitively establish the role of CES1 in mediating (V)LDL-cholesterol production by the compounds, and iii) determine the efficacy of the compounds in lowering cholesterol and steatosis humanized mouse models.

Key facts

NIH application ID
10913480
Project number
5R01DK136328-02
Recipient
MEDICAL UNIVERSITY OF SOUTH CAROLINA
Principal Investigator
STEPHEN A DUNCAN
Activity code
R01
Funding institute
NIH
Fiscal year
2024
Award amount
$512,957
Award type
5
Project period
2023-09-01 → 2027-08-31