Reference : Novel synthetic pyridyl analogues of CDDO-Imidazolide are useful new tools in cancer ...
Scientific journals : Article
Human health sciences : Pharmacy, pharmacology & toxicology
http://hdl.handle.net/2268/192120
Novel synthetic pyridyl analogues of CDDO-Imidazolide are useful new tools in cancer prevention.
English
Cao, Martine mailto [Dartmouth Medical School > > > >]
Onyango, Evans O. [> >]
Williams, Charlotte R. [> >]
Royce, Darlene B. [> >]
Gribble, Gordon W. [> >]
Sporn, Michael B. [> >]
Liby, Karen T. [> >]
2015
Pharmacological Research
100
135-47
Yes (verified by ORBi)
International
1043-6618
1096-1186
Netherlands
[en] CDDO-Imidazolide ; Chemoprevention ; HO-1 ; Lung carcinogenesis ; NQO1 ; Nitric oxide ; Nrf2 ; Pyridyl analogues ; Vinyl carbamate
[en] Two new analogues of CDDO-Imidazolide (CDDO-Im), namely 1-[2-Cyano-3,12-dioxooleana-1,9(11)-dien-28-oyl]-4(-pyridin-2-yl)-1H-imidazole ("CDDO-2P-Im") and 1-[2-Cyano-3,12-dioxooleana-1,9(11)-dien-28-oyl]-4(-pyridin-3-yl)-1H-imidazole ("CDDO-3P-Im") have been synthesized and tested for their potential use as chemopreventive drugs. At nanomolar concentrations, they were equipotent to CDDO-Im for inducing differentiation and apoptosis in U937 leukemia cells. As inflammation and oxidative stress contribute to carcinogenesis, we also assessed their cytoprotective potential. The new compounds suppressed inducible nitric oxide synthase (iNOS) expression in RAW264.7 macrophage-like cells and significantly elevated heme oxygenase-1 (HO-1) and quinone reductase (NQO1) mRNA and protein levels in various mouse tissues in vivo. Most importantly, pharmacokinetic studies performed in vitro in human plasma and in vivo showed that each new analogue was more stable than CDDO-Im. Much higher concentrations of the new derivatives were found in mouse liver, lung, pancreas and kidney after gavage in contrast to CDDO-Im. Because of their better bioavailability and their excellent anti-inflammatory profile in vitro, CDDO-2P-Im and CDDO-3P-Im were tested for prevention in a highly relevant mouse lung cancer model, in which A/J mice develop lung carcinomas after injection of vinyl carbamate, a potent carcinogen. CDDO-2P-Im and CDDO-3P-Im were as effective as CDDO-Im for reducing the size and the severity of the lung tumors.
http://hdl.handle.net/2268/192120
Copyright (c) 2015 Elsevier Ltd. All rights reserved.

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