Target intelligence / Profile preview

Long-chain fatty acid transport protein 2 (FATP2)

Target
FATP2
Molecular classification
Transporter, Enzyme (Acyl-CoA synthetase), Solute carrier (SLC) family member
01

Overview

Long-chain fatty acid transport protein 2 (FATP2), encoded by the SLC27A2 gene, is a bifunctional membrane protein with both transporter and enzymatic (acyl-CoA synthetase) activity, primarily expressed in the liver, kidney, and placenta[2][3][7]. FATP2 facilitates the uptake and simultaneous activation (to acyl-CoA esters) of long-chain and very long-chain fatty acids, which is essential for lipid biosynthesis and fatty acid degradation through β-oxidation in peroxisomes and the endoplasmic reticulum. Besides its metabolic roles, FATP2 is implicated in immunosuppression in cancer via the regulation of arachidonic acid uptake and prostaglandin synthesis by myeloid-derived suppressor cells, influences nonalcoholic fatty liver disease progression, and is associated with the pathology of X-linked adrenoleukodystrophy due to compromised peroxisomal fatty acid activation[1][3][5]. Tool compounds inhibiting FATP2 are under investigation for cancer therapy and metabolic disease, but modulation may carry risks of fundamental disruptions in systemic fatty acid metabolism.

Other names
SLC27A2Acyl-CoA synthetase very long-chain 1 (ACSVL1)Fatty acid transport protein 2 (FATP2)Very long-chain acyl-CoA synthetase (VLACS)Fatty-acid-coenzyme A ligase, very long-chain 1Long-chain-fatty-acid--CoA ligasePhytanate--CoA ligaseTHCA-CoA ligaseArachidonate--CoA ligaseSolute carrier family 27 member 2
02

Mechanism of action

Inhibition of fatty acid uptake (by blocking transporter function); Inhibition of acyl-CoA synthetase activity (by blocking fatty acid activation)

03

Biological functions

Fatty acid uptake and transportFatty acid activation (acyl-CoA synthesis)Lipid biosynthesisFatty acid degradation (via CoA ester formation)Cellular energy metabolism
04

Disease associations

Cancer (notably immunosuppression and tumor progression)Metabolic disease (NAFLD, steatosis)X-linked adrenoleukodystrophy (via defective peroxisomal very long-chain fatty acid metabolism)Chronic kidney diseaseOther disorders of lipid metabolism
05

Safety considerations

Metabolic dysregulation (e.g., potential for lipotoxicity or impaired energy metabolism if blocked systemically)Risk of steatosis or fatty acid accumulation in tissues[1][5]Effects on fetal fatty acid supply in pregnancy[7]
06

Interacting drugs

Lipofermata (small molecule inhibitor)

2 more in the full profile.

07

Biomarkers

SLC27A2/FATP2 expression in tumors (for immunosuppressive myeloid-derived suppressor cell activity, prognosis, and therapy response in cancer)[5]Expression in kidney and placenta as markers for fatty acid transport function in these tissues[7]

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