Conjugated Linoleic Acid Ameliorates Inflammation-Induced Colorectal Cancer in Mice through Activation of PPARγ

被引:95
作者
Evans, Nicholas P. [1 ]
Misyak, Sarah A. [1 ]
Schmelz, Eva M. [1 ]
Guri, Amir J. [1 ]
Hontecillas, Raquel [1 ]
Bassaganya-Riera, Josep [1 ]
机构
[1] Virginia Polytech Inst & State Univ, Virginia Bioinformat Inst, Nutr Immunol & Mol Nutr Lab, Blacksburg, VA 24061 USA
关键词
POLYUNSATURATED FATTY-ACIDS; T-CELL RESPONSES; RECEPTOR-GAMMA; COLON CARCINOGENESIS; GENE-EXPRESSION; INDUCED COLITIS; BOWEL-DISEASE; BETA-CATENIN; MACROPHAGES; PROTECTION;
D O I
10.3945/jn.109.115642
中图分类号
R15 [营养卫生、食品卫生]; TS201 [基础科学];
学科分类号
100403 ;
摘要
Conjugated linoleic acid (CLA) exerts a protective effect on experimental inflammatory bowel disease and shows promise as a chemopreventive agent against colorectal cancer (CRC) in mice, although the mechanisms by which it exerts its beneficial effects against malignancies in the gut are not completely understood. Mice lacking PPAR gamma in immune and epithelial cells and PPAR gamma-expressing littermates were fed either control or CLA-supplemented (1 g CLA/100 g) diets to determine the role of PPAR gamma in inflammation-induced CRC. To induce tumor formation and colitis, mice were treated with azoxymethane and then challenged with 2% dextran sodium sulfate, respectively. Dietary CLA ameliorated disease activity, decreased colitis, and prevented adenocarcinoma formation in the PPAR gamma-expressing floxed mice but not in the tissue-specific PPAR gamma-null mice. Dietary CLA supplementation significantly decreased the percentages of macrophages in the mesenteric lymph nodes (MLN) regardless of the genotype and increased regulatory T cell numbers in MLN of PPAR gamma-expressing, but not in the tissue-specific, PPAR gamma-null mice. Colonic tumor necrosis factor-alpha mRNA expression was significantly suppressed in CLA-fed, PPAR gamma-expressing mice. This study suggests CLA ameliorates colitis and prevents tumor formation in part through a PPAR gamma-dependent mechanism. J. Nutt. 140: 515-521, 2010.
引用
收藏
页码:515 / 521
页数:7
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