Target intelligence / Profile preview

Cell death-inducing DFFA-like effector C (CIDEC)

Target
CIDEC
Molecular classification
Lipid droplet-associated protein, Other (cell death-inducing DNA fragmentation factor-like effector family)
01

Overview

Cell death-inducing DFFA-like effector C (CIDEC, also known as FSP27 in mice) is a lipid droplet–associated protein that plays a central role in adipocyte biology by promoting the formation of large, unilocular lipid droplets through facilitation of droplet fusion and lipid exchange and by inhibiting lipolysis[1][3][4][6]. CIDEC thereby optimizes triglyceride storage, prevents excessive free fatty acid release, and ensures efficient energy storage[1][2][3]. The protein is regulated by insulin, and its expression correlates positively with insulin sensitivity[1][3]. CIDEC also plays a role in apoptosis, particularly under metabolic stress or specific experimental conditions[1][3]. Mutations or altered expression patterns are associated with metabolic diseases, including familial partial lipodystrophy, type 5, insulin resistant diabetes, and fatty liver diseases[1][3][4]. Distinct tissue-specific isoforms contribute to fat storage in adipose and triglyceride accumulation in the liver, particularly under metabolic or ethanol-induced stress[1]. No direct drug modulators of CIDEC are currently approved, but its role in energy homeostasis and cell death makes it a potential target for therapies aimed at metabolic diseases[1][3].

Other names
CIDE-3FSP27CIDE3FLJ20871FPLD5fat-specific protein 27cell death activator CIDE-3lipid transferase CIDECcell death-inducing DFFA-like effector protein Cfat-specific protein FSP27 homolog
02

Mechanism of action

Not established for specific drugs; mechanism as a target would involve modulation of lipid droplet formation, inhibition of lipolysis, adipocyte apoptosis, and regulation of triglyceride storage

03

Biological functions

Lipid droplet morphology and fusionTriglyceride storage regulationInhibition of lipolysisPromotion of unilocular lipid droplet formationApoptosis mediation
04

Disease associations

Lipodystrophy (familial partial, type 5)Insulin resistance/diabetesNonalcoholic and alcoholic fatty liver diseasesOther metabolic disorders
05

Safety considerations

Disruption leads to impaired energy storage, abnormal adipocyte morphology, and increased risk of insulin resistance, diabetes, hepatic steatosis, and other metabolic syndrome sequelae
06

Biomarkers

Mutations in CIDEC associated with familial partial lipodystrophyElevated expression in nonalcoholic fatty liver disease and insulin sensitive statesAlternative hepatic isoforms (e.g., FSP27β) upregulated by metabolic stress

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