Target intelligence / Profile preview

Sterol regulatory element-binding transcription factor 1c (SREBP-1c)

Target
SREBP-1c
Molecular classification
Transcription factor, Basic helix-loop-helix-leucine zipper (bHLH-Zip) family
01

Overview

Sterol regulatory element-binding transcription factor 1c (SREBP-1c) is an isoform of the protein family encoded by the *SREBF1* gene, produced by alternative promoter selection. SREBP-1c is a membrane-bound precursor that, upon activation, translocates to the nucleus where it binds sterol regulatory elements in DNA and drives the transcription of genes involved primarily in fatty acid synthesis and aspects of glucose metabolism. It is predominantly expressed in the liver, muscle, and adipose tissue and is highly regulated by nutritional and hormonal signals, especially insulin and sterols. SREBP-1c activity is associated with oncogenic transformation, metabolic disease, and lipid-dependent pathologies. Its dysregulation has implications in non-alcoholic fatty liver disease, type 2 diabetes, cancer cell proliferation (notably in clear cell renal cell carcinoma), and other disorders connected to lipid metabolism. SREBP-1c is considered a key therapeutic and diagnostic target for interventions aiming at metabolic pathways and cell cycle progression.

Other names
Sterol regulatory element-binding protein 1cSREBP-1cADD-1SREBF1c
02

Mechanism of action

Drugs (e.g., LXR agonists) increase SREBP-1c-mediated gene transcription, enhancing lipogenesis. HMG CoA reductase inhibitors suppress cholesterol synthesis, lowering SREBP-1c expression. Fatty acid synthase and acetyl-CoA carboxylase inhibitors disrupt downstream lipid synthesis.

03

Biological functions

Lipogenesis regulationTranscriptional activation of genes for fatty acid synthesisCell cycle regulation and cell proliferationGlucose metabolism
04

Disease associations

Cancer (especially clear cell renal cell carcinoma and tumor cell metabolism)Metabolic diseases (obesity, type 2 diabetes, fatty liver/steatosis)Hereditary syndromes (Mucoepithelial dysplasia, Ifap syndrome 2)Cardiovascular disease (via lipid regulation)
05

Safety considerations

Excess SREBP-1c activity promotes hepatic steatosis and contributes to insulin resistanceRisk of tumorigenesis due to enhanced cell proliferation/lipid accretionMetabolic complications from drug-mediated lipid changes
06

Interacting drugs

LXR agonists (e.g., T0901317, 22(R)-hydroxycholesterol)

3 more in the full profile.

07

Biomarkers

SREBP-1c mRNA/protein expression (for tumor proliferation and fatty liver)Target gene products (e.g., PCNA, cyclin A, PTTG1 in cell cycle, glucokinase in glycolysis)

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