Target intelligence / Profile preview

Cytochrome P450 family 4 subfamily F member 8 (CYP4F8)

Target
CYP4F8
Molecular classification
Enzyme, Oxidoreductase, Cytochrome P450 (heme-containing monooxygenase), Microsomal monooxygenase
01

Overview

Cytochrome P450 family 4 subfamily F member 8 (CYP4F8) is a microsomal monooxygenase enzyme belonging to the cytochrome P450 superfamily. CYP4F8 catalyzes omega-1 and omega-2 hydroxylation of prostaglandins (especially PGH1, PGH2, and PGI2) and polyunsaturated fatty acids, and performs epoxidation reactions on long-chain fatty acids. It is most highly expressed in human seminal vesicles and various epithelial tissues, supporting the formation of 19-hydroxy prostaglandins—predominant in seminal fluid—through lipid oxidations. Recombinant studies show CYP4F8 also generates specific eicosanoid metabolites that regulate inflammation and tissue function. Dysregulation of CYP4F8 is implicated in prostate cancer, where elevated activity may support cell growth, and in skin diseases (psoriasis), where altered expression affects keratinocyte proliferation and lipid oxidative balance. CYP4F8 is part of a cluster of cytochrome P450 genes on chromosome 19. No clinical drugs currently target CYP4F8 directly, but its tissue-selective liability and role in disease make it a candidate therapeutic target for future research.

Other names
Cytochrome P450 4F8CYP4F8CYPIVF8CPF8Cytochrome P450, family 4, subfamily F, polypeptide 8Cytochrome P450, subfamily IVF, polypeptide 8Flavoprotein-linked monooxygenaseMicrosomal monooxygenase
02

Mechanism of action

Not applicable: No clinical drugs specifically approved to target CYP4F8 thus far. Interaction with endogenous substrates (prostaglandins, fatty acids): primarily hydroxylation and epoxidation as monooxygenase

03

Biological functions

Lipid oxidation (including hydroxylation and epoxidation of fatty acids)Metabolism of prostaglandins and eicosanoidsDrug metabolism (minor role compared to major P450s)Synthesis of cholesterol, steroids, and other lipidsRegulation of lipid signaling in specific tissues
04

Disease associations

Cancer (notably dysregulated in prostate cancer; supports cell growth and survival)Inflammation (e.g., induced expression in psoriatic lesions; may affect keratinocyte proliferation)Other—Rare inherited eye and metabolic disorders (Bietti crystalline corneoretinal dystrophy, Refsum disease)Possible role in disorders of lipid homeostasis or skin/epithelial pathologies
05

Safety considerations

No documented safety liabilities for CYP4F8 inhibition or modulation; risks typical for cytochrome P450s would be off-target metabolic changes or impact on lipid signalingDysregulation may influence cell proliferation or lipid metabolite balance
06

Interacting drugs

No major small-molecule drugs directly targeting CYP4F8 are approved. Most cytochrome P450 drug interactions involve other isoforms (e.g., CYP3A4, CYP2D6), and there is no evidence of clinical CYP4F8 inhibitors or activators
07

Biomarkers

Overexpression in prostate cancer (potential biomarker for disease state or therapy selection)Induction in psoriatic skin lesions (potential for skin disease biomarker)

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