Abstract |
The Cytochrome P450 4 ( CYP4) family of enzymes in humans is comprised of thirteen isozymes that typically catalyze the ω-oxidation of endogenous fatty acids and eicosanoids. Several CYP4 enzymes can biosynthesize 20- hydroxyeicosatetraenoic acid, or 20-HETE, an important signaling eicosanoid involved in regulation of vascular tone and kidney reabsorption. Additionally, accumulation of certain fatty acids is a hallmark of the rare genetic disorders, Refsum disease and X-ALD. Therefore, modulation of CYP4 enzyme activity, either by inhibition or induction, is a potential strategy for drug discovery. Here we review the substrate specificities, sites of expression, genetic regulation, and inhibition by exogenous chemicals of the human CYP4 enzymes, and discuss the targeting of CYP4 enzymes in the development of new treatments for hypertension, stroke, certain cancers and the fatty acid-linked orphan diseases.
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Authors | Katheryne Z Edson, Allan E Rettie |
Journal | Current topics in medicinal chemistry
(Curr Top Med Chem)
Vol. 13
Issue 12
Pg. 1429-40
( 2013)
ISSN: 1873-4294 [Electronic] United Arab Emirates |
PMID | 23688133
(Publication Type: Journal Article, Research Support, N.I.H., Extramural, Review)
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Chemical References |
- Cytochrome P-450 Enzyme Inhibitors
- Hydroxyeicosatetraenoic Acids
- 20-hydroxy-5,8,11,14-eicosatetraenoic acid
- Cytochrome P-450 Enzyme System
- Cytochrome P-450 CYP4A
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Topics |
- Animals
- Cytochrome P-450 CYP4A
(antagonists & inhibitors, metabolism)
- Cytochrome P-450 Enzyme Inhibitors
- Cytochrome P-450 Enzyme System
(genetics, metabolism)
- Humans
- Hydroxyeicosatetraenoic Acids
(biosynthesis, chemistry)
- Molecular Structure
- Molecular Targeted Therapy
- Structure-Activity Relationship
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