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Published Online
on August 17, 2006

Arteriosclerosis, Thrombosis, and Vascular Biology. 2006
Published online before print August 17, 2006, doi: 10.1161/01.ATV.0000242013.29441.81
A more recent version of this article appeared on November 1, 2006
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Submitted on July 18, 2006
Accepted on August 4, 2006

Inhibition of Smooth Muscle Proliferation by Urea-Based Alkanoic Acids via Peroxisome Proliferator-Activated Receptor {alpha}-Dependent Repression of Cyclin D1

Valerie Y. Ng ; Christophe Morisseau ; John R. Falck ; Bruce D. Hammock ; and Deanna L. Kroetz *

From the Department of Biopharmaceutical Sciences (V.Y.N., D.L.K.), the Center for Human Genetics (D.L.K.), and the Liver Center (D.L.K.), University of California, San Francisco; Department of Entomology and the Cancer Research Center (C.M., B.D.H), University of California, Davis; and Department of Biochemistry (J.R.F.), University of Texas Southwestern Medical Center, Dallas.

* To whom correspondence should be addressed. E-mail: deanna.kroetz{at}ucsf.edu.

Objective--Proliferation of smooth muscle cells is implicated in cardiovascular complications. Previously, a urea-based soluble epoxide hydrolase inhibitor was shown to attenuate smooth muscle cell proliferation. We examined the possibility that urea-based alkanoic acids activate the nuclear receptor peroxisome proliferator-activated receptor {alpha} (PPAR{alpha}) and the role of PPAR{alpha} in smooth muscle cell proliferation.

Methods and Results--Alkanoic acids transactivated PPAR{alpha}, induced binding of PPAR{alpha} to its response element, and significantly induced the expression of PPAR{alpha}-responsive genes, showing their function as PPAR{alpha} agonists. Furthermore, the alkanoic acids attenuated platelet-derived growth factor-induced smooth muscle cell proliferation via repression of cyclin D1 expression. Using small interfering RNA to decrease endogenous PPAR{alpha} expression, it was determined that PPAR{alpha} was partially involved in the cyclin D1 repression. The antiproliferative effects of alkanoic acids may also be attributed to their inhibitory effects on soluble epoxide hydrolase, because epoxyeicosatrienoic acids alone inhibited smooth muscle cell proliferation.

Conclusions--These results show that attenuation of smooth muscle cell proliferation by urea-based alkanoic acids is mediated, in part, by the activation of PPAR{alpha}. These acids may be useful for designing therapeutics to treat diseases characterized by excessive smooth muscle cell proliferation.




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V. Y. Ng, Y. Huang, L. M. Reddy, J. R. Falck, E. T. Lin, and D. L. Kroetz
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