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Publication : Endogenous conversion of ω-6 to ω-3 polyunsaturated fatty acids in fat-1 mice attenuated intestinal polyposis by either inhibiting COX-2/β-catenin signaling or activating 15-PGDH/IL-18.

First Author  Han YM Year  2016
Journal  Int J Cancer Volume  138
Issue  9 Pages  2247-56
PubMed ID  26650508 Mgi Jnum  J:237658
Mgi Id  MGI:5816421 Doi  10.1002/ijc.29956
Citation  Han YM, et al. (2016) Endogenous conversion of omega-6 to omega-3 polyunsaturated fatty acids in fat-1 mice attenuated intestinal polyposis by either inhibiting COX-2/beta-catenin signaling or activating 15-PGDH/IL-18. Int J Cancer 138(9):2247-56
abstractText  Omega-3 polyunsaturated fatty acids (omega-3PUFAs) have inhibitory effects in various preclinical cancer models, but their effects in intestinal polyposis have never been examined. As attempts have been made to use nutritional intervention to counteract colon cancer development, in this study we evaluated the effects of omega-3 PUFAs on intestinal polyposis in the Apc(Min/+) mouse model. The experimental groups included wild-type C56BL/6 mice, Apc(Min/+) mice, fat-1 transgenic mice expressing an n-3 desaturase to enable omega-3 PUFA synthesis, and Apc(Min/+) x fat-1 double-transgenic mice; all mice were 20 weeks of age. Small intestines were collected for gross and pathologic evaluation, including assessment of polyp number and size, followed by immunohistochemical staining and Western blotting. After administration of various concentrations of omega-3 PUFAs, PUFA levels were measured in small intestine tissue by GC/MS/MS analysis to compare with PUFA synthesis of between C57BL6 and fat-1mice. As a result, omega-3 PUFAs significantly attenuated Apc mutation-induced intestinal polyposis accompanied with significant inhibition of Wnt/beta-catenin signaling, COX-2 and PGE2, but induced significant levels of 15-PGDH. In addition, significant induction of the inflammasome-related substrates as IL-1beta and IL-18 and activation of caspase-1 was observed in Apc(Min/+) x fat-1 mice. Administration of at least 3 g/60 kg omega-3 PUFAs was equivalent to omega-3 PUFAs produced in fat-1 mice and resulted in significant increase in the expression of IL-1beta, caspase-3 and IL-18, as seen in Apc(Min/+) x fat-1 mice. We conclude that omega-3PUFAs can prevent intestinal polyp formation by inhibition of Wnt/beta-catenin signaling, but increased levels of 15-PGDH and IL-18.
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