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Carcinogenesis Advance Access originally published online on July 4, 2003
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Carcinogenesis, Vol. 24, No. 9, 1541-1548, September 2003
© 2003 Oxford University Press


MOLECULAR EPIDEMIOLOGY AND CANCER PREVENTION

Chemopreventive n-3 fatty acids activate RXR{alpha} in colonocytes

Yang-Yi Fan1, Thomas E. Spencer2,3, Naisyin Wang4, Mary P. Moyer5,{dagger} and Robert S. Chapkin1,3,6

1 Faculty of Nutrition, Texas A&M University, College Station, TX 77843, USA
2 Center for Environmental and Rural Health, Texas A&M University, College Station, TX 77843, USA
3 Department of Animal Science, Texas A&M University, College Station, TX 77843, USA
4 Department of Statistics, Texas A&M University, College Station, TX 77843, USA
5 INCELL Corporation, San Antonio, TX 78249, USA

6 To whom correspondence should be addressed Email: r-chapkin{at}tamu.edu

The underlying mechanisms by which n-3 polyunsaturated fatty acids (PUFA) exert a chemopreventive effect in the colon have not been elucidated. Retinoid X receptors (RXR) are a family of nuclear receptors implicated in cancer chemoprevention. Since docosahexaenoic acid (DHA), an n-3 PUFA enriched in fish oil, reduces colonocyte proliferation and enhances apoptosis relative to n-6 PUFA-treated cells, we determined whether DHA can serve as a specific ligand for RXR{alpha} activation relative to n-6 PUFA in colonocytes. In a mammalian one-hybrid assay, immortalized young adult mouse colonic (YAMC) cells were co-transfected with a yeast galactose upstream activating sequence (UAS)4-tk-Luciferase (Luc) reporter plasmid, plus either GAL4 DNA-binding domain fused to RXR{alpha}, retinoic acid receptor {alpha} or GAL4 alone, followed by an n-3, n-6 or n-9 fatty acid incubation. Luc activity levels were dose-dependently elevated only in n-3 PUFA (DHA)-treated RXR{alpha}. Since RXR homodimers and RXR/peroxisome proliferator-activated receptor (PPAR) heterodimers bind consensus direct repeat (DR1) motifs, YAMC and NCM460 (a normal human colonic cell line), were respectively, co-transfected with RXR{alpha} and DR1-Luc, followed by different PUFA treatment. Luc activity levels were increased (P < 0.05) only in DHA groups. The DHA-dependent induction of DR-1-Luc was reduced to basal levels upon RXR{alpha} antagonist-treatment, with no effect on PPAR{gamma} antagonist-treatment. A role for select RXR isoforms in colonocyte biology was also determined by examining nuclear receptor mRNA levels in rat colon following dietary lipid and carcinogen exposure over time. RXR{alpha}, RXRß and RXR{gamma} were detected in rat colonic mucosa, and the levels of RXR{alpha} and RXR{gamma} were elevated in fish oil (n-3 PUFA) versus corn oil (n-6 PUFA) fed animals after 16 weeks. These data indicate that, RXR{alpha}, an obligatory component of various nuclear receptors, preferentially binds n-3 PUFA in colonocytes, and that the nuclear receptor targets for PUFA in the colon are modulated by dietary lipid exposure.


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