Cytochrome P450 epoxygenases and cancer: A genetic and a molecular perspective.

Angiogenesis Cancer Endothelial cells Growth factors Lipids Single nucleotide polymorphism

Journal

Pharmacology & therapeutics
ISSN: 1879-016X
Titre abrégé: Pharmacol Ther
Pays: England
ID NLM: 7905840

Informations de publication

Date de publication:
04 2019
Historique:
pubmed: 7 12 2018
medline: 28 3 2020
entrez: 7 12 2018
Statut: ppublish

Résumé

Cytochrome CYP450 epoxygenases catalyze the epoxidation of polyunsaturated fatty acids including arachidonic acid, eicosapentaenoic acid, and docosahexaenoic acid. The arachidonic acid-derived products are potent pro-angiogenic lipids and promote tumor development and growth. On the other hand, eicosapentaenoic acid- and docosahexaenoic acid-derived products inhibit angiogenesis and play a protective role in certain pathological conditions including cancer. Increased expression of CYP2C epoxygenases, together with increased levels of their arachidonic acid-derived products, is often observed in tumors and tumor-associated vasculature, making these enzymes an ideal target for anti-cancer therapies. Yet, given the pro- and anti-angiogenic action of these enzymes, a better understanding of the specific roles of their products in the regulation of endothelial cell function and cancer development is required. In this review, we provide an overview of the role of CYP450 epoxygenase-derived lipids, with emphasis on arachidonic acid-derived products, in the regulation of endothelial cell function both in physiological and pathological conditions. Moreover, we discuss the impact of genetic polymorphisms in CYP450 epoxygenases on cancer risk, and we discuss advantages and limitation of approaches to target these enzymes and their products in pathological angiogenesis and cancer.

Identifiants

pubmed: 30521883
pii: S0163-7258(18)30214-6
doi: 10.1016/j.pharmthera.2018.11.009
pii:
doi:

Substances chimiques

Arachidonic Acid 27YG812J1I
Cytochrome P-450 Enzyme System 9035-51-2

Types de publication

Journal Article Research Support, N.I.H., Extramural Research Support, U.S. Gov't, Non-P.H.S. Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

183-194

Subventions

Organisme : NCI NIH HHS
ID : T32 CA094186
Pays : United States
Organisme : NCI NIH HHS
ID : R01 CA162433
Pays : United States
Organisme : NIDDK NIH HHS
ID : R01 DK119212
Pays : United States
Organisme : NIDDK NIH HHS
ID : P30 DK114809
Pays : United States

Informations de copyright

Copyright © 2018 Elsevier Inc. All rights reserved.

Auteurs

Lindsay N Sausville (LN)

Department of Population and Quantitative Health Science, Case Western Reserve University, Cleveland, OH, United States.

Scott M Williams (SM)

Department of Population and Quantitative Health Science, Case Western Reserve University, Cleveland, OH, United States.

Ambra Pozzi (A)

Division of Nephrology and Hypertension, Department of Medicine, Vanderbilt University Medical Center, Nashville, TN, United States; Department of Veterans Affairs, Nashville, TN, United States. Electronic address: ambra.pozzi@vumc.org.

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Classifications MeSH