Target intelligence / Profile preview

Peroxisome proliferator-activated receptor delta (PPARδ) (PPARδ)

Target
PPARδ
Molecular classification
Nuclear receptor, Transcription factor, Ligand-activated transcription factor
01

Overview

Peroxisome proliferator-activated receptor delta (PPARδ), also known as PPARβ, is a ligand-activated transcription factor belonging to the nuclear receptor superfamily (UniProt: P16671). It is ubiquitously expressed but found at high levels in tissues with high fatty acid oxidation rates, such as skeletal muscle, heart, and adipose tissue (PubMed: 26073486). PPARδ plays a critical role in regulating lipid metabolism, glucose homeostasis, and energy expenditure by promoting the expression of genes involved in fatty acid uptake and beta-oxidation (NCBI Gene: 5467). Beyond metabolism, it exerts anti-inflammatory effects and is involved in wound healing and cell differentiation (PubMed: 12665521). In clinical medicine, PPARδ is a major therapeutic target for metabolic and hepatic diseases, including dyslipidemia, nonalcoholic steatohepatitis (NASH), and primary biliary cholangitis (PBC) (PubMed: 31513942). Drugs targeting this receptor, such as seladelpar and elafibranor, act as agonists to improve lipid profiles and reduce hepatic inflammation and fibrosis (ClinicalTrials.gov: NCT03602560). However, concerns regarding potential pro-carcinogenic effects observed in preclinical rodent models have historically complicated its drug development path (PubMed: 23536517).

Other names
Peroxisome proliferator-activated receptor betaPPAR-deltaPPAR-betaNR1C2Nuclear receptor subfamily 1 group C member 2NUC1
02

Mechanism of action

Agonism; the receptor forms a heterodimer with the Retinoid X Receptor (RXR) upon ligand binding, which then binds to Peroxisome Proliferator Response Elements (PPREs) in the promoter regions of target genes to modulate their transcription.

03

Biological functions

Lipid metabolismFatty acid oxidationGlucose homeostasisInflammation modulationMitochondrial biogenesisWound healing
04

Disease associations

DyslipidemiaMetabolic syndromeNonalcoholic steatohepatitisPrimary biliary cholangitisObesityType 2 diabetesCardiovascular disease
05

Safety considerations

Potential carcinogenicity (based on high-dose rodent studies)Liver toxicityMuscle toxicityPotential for off-target nuclear receptor activation
06

Interacting drugs

Seladelpar

4 more in the full profile.

07

Biomarkers

Alkaline phosphatase (ALP)High-density lipoprotein cholesterol (HDL-C)TriglyceridesGamma-glutamyl transferase (GGT)C-reactive protein (CRP)

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