4.6 Article

Western-style diets induce macrophage infiltration and contribute to colitis-associated carcinogenesis

Journal

JOURNAL OF GASTROENTEROLOGY AND HEPATOLOGY
Volume 25, Issue 11, Pages 1785-1794

Publisher

WILEY
DOI: 10.1111/j.1440-1746.2010.06332.x

Keywords

colitis; macrophages; neoplasms; prostaglandin-endoperoxide synthase 2; western-style diet

Funding

  1. National Research Foundation of Korea
  2. Ministry of Education, Science and Technology [KRF-2008-313-E00437]
  3. Ministry of Health, Welfare and Family [A062254]
  4. Korean Research Institute of Bioscience Technology [KGM2210911]
  5. National Research Council of Science & Technology (NST), Republic of Korea [KGM2210911] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)

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Background and Aim: A Western-style diet (WD) is known to play an important role in inflammatory bowel disease and colon carcinogenesis. The purpose of this study was to understand the role of macrophages in WD-induced colitis associated with carcinogenesis. Methods: Male BALB/c mice were fed a WD or a control diet (CD) for 4 weeks and exposed to azoxymethane (AOM) followed by 2% dextran sulfate sodium (DSS) for 7 days. Results: The WD increased susceptibility to DSS-induced inflammation and accelerated the infiltration of macrophages. The incidence and multiplicity of colon tumors were higher in mice fed the WD than in those fed the CD (P < 0.05). Levels of prostaglandin-endoperoxide synthase (PTGS) 2 and prostaglandin (PG) E-2 in the colon were higher after treatment with AOM and DSS in mice fed the WD than in those fed the CD. In addition, WD consumption increased the DNA binding activity of nuclear factor-kappaB and the serum concentration of tumor necrosis factor (TNF)-alpha. Mice fed the WD had higher numbers of F4/80-positive cells surrounding cancer cells compared with mice fed the CD. These cells expressed PTGS2, TNF-alpha and beta-catenin, which are up-regulated by the WD. We also found that the WD increased unphosphorylated beta-catenin accumulation in the cytoplasm and nucleus of colon cancer cells. Conclusions: A WD increases the susceptibility to DSS-induced inflammation and accelerates the infiltration of macrophages. In turn, this resulted in the development and progression of colon cancer.

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