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Differential proto-oncogene mRNA induction from rats treated with peroxisome proliferators.

作者信息

Cherkaoui Malki M, Lone Y C, Corral-Debrinski M, Latruffe N

机构信息

Laboratoire de Biochimie et Biologie Moléculaire (URA CNRS 531), Université de Franche Comté, Besançon, France.

出版信息

Biochem Biophys Res Commun. 1990 Dec 31;173(3):855-61. doi: 10.1016/s0006-291x(05)80865-4.

Abstract

After experimental treatment of rats with clofibrate or ciprofibrate, two peroxisomes proliferators with hypolipidemic activity, RNAs were prepared from liver, kidney, heart and brain; hybridization was done with DNA probes for c-myc and c-Ha-ras oncogenes and for cyanide insensitive Acyl CoA oxidase, a peroxisomal protein. c-myc mRNA is highly abundant in liver and at a lower extent in kidney, especially after treatment with ciprofibrate; clofibrate also allows a c-myc mRNA increase, but at a lower extent. c-Ha-ras, which is already expressed in all tested tissues from control animals, is stimulated by clofibrate and ciprofibrate treatments. Comparatively these compounds stimulate the cyanide insensitive Acyl CoA oxidase expression as well as they increase the somatic index of liver and kidney. From these experiments we suggest that hepatocarcinogenesis triggered by some hypolipidemic agents could be mediated by proto-oncogene mRNA level increase.

摘要

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