Diminished hepatocellular proliferation in mice humanized for the nuclear receptor peroxisome proliferator-activated receptor α

• Published in: Cancer research (Chicago, Ill.) Vol. 64; no. 11; pp. 3849 - 3854
• Main Authors: CHEUNG, Connie, AKIYAMA, Taro E, WARD, Jerrold M, NICOL, Christopher J, FEIGENBAUM, Lionel, VINSON, Charles, GONZALEZ, Frank J
• Format: Journal Article
• Language: English
• Published: Philadelphia, PA American Association for Cancer Research 01.06.2004
• Subjects: Animals; Anticholesteremic Agents - pharmacology; Antineoplastic agents; Biological and medical sciences; Carcinogens - pharmacology; Cell Division; DNA Replication - drug effects; Fatty Acids - metabolism; Hepatocytes - cytology; Hepatocytes - drug effects; Hepatocytes - metabolism; Hepatocytes - physiology; Humans; Medical sciences; Mice; Mice, Transgenic; Oxidation-Reduction; Peroxisome Proliferators - pharmacology; Pharmacology. Drug treatments; Pyrimidines - pharmacology; Receptors, Cytoplasmic and Nuclear - genetics; Receptors, Cytoplasmic and Nuclear - physiology; Species Specificity; Transcription Factors - genetics; Transcription Factors - physiology; Tumors; Cell proliferation; Vertebrata; Nuclear receptor; Mammalia; Mouse; Animal; Rodentia; Peroxisome proliferator activated receptor
• ISSN: 0008-5472; 1538-7445
• DOI: 10.1158/0008-5472.CAN-04-0322

Lipid-lowering fibrate drugs function as agonists for the nuclear receptor peroxisome proliferator-activated receptor alpha (PPARalpha). Sustained activation of PPARalpha leads to the development of liver tumors in rats and mice. However, humans appear to be resistant to the induction of peroxisome proliferation and the development of liver cancer by fibrate drugs. The molecular basis of this species difference is not known. To examine the mechanism determining species differences in peroxisome proliferator response between mice and humans, a PPARalpha-humanized mouse line was generated in which the human PPARalpha was expressed in liver under control of the tetracycline responsive regulatory system. The PPARalpha-humanized and wild-type mice responded to treatment with the potent PPARalpha ligand Wy-14643 as revealed by induction of genes encoding peroxisomal and mitochondrial fatty acid metabolizing enzymes and resultant decrease of serum triglycerides. However, surprisingly, only the wild-type mice and not the PPARalpha-humanized mice exhibited hepatocellular proliferation as revealed by elevation of cell cycle control genes, increased incorporation of 5-bromo-2'-deoxyuridine into hepatocyte nuclei, and hepatomegaly. These studies establish that following ligand activation, the PPARalpha-mediated pathways controlling lipid metabolism are independent from those controlling the cell proliferation pathways. These findings also suggest that structural differences between human and mouse PPARalpha are responsible for the differential susceptibility to the development of hepatocarcinomas observed after treatment with fibrates. The PPARalpha-humanized mice should serve as models for use in drug development and human risk assessment and to determine the mechanism of hepatocarcinogenesis of peroxisome proliferators.