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Diet-induced obesity elevates colonic TNF-α in mice and is accompanied by an activation of Wnt signaling: a mechanism for obesity-associated colorectal cancer

  • Zhenhua Liu

      Affiliations

    • Vitamins and Carcinogenesis Laboratory, Jean Mayer USDA Human Nutrition Research Center on Aging, Tufts University, Boston, MA 02111, USA
    • Friedman School of Nutrition Science and Policy, Tufts University, Boston, MA 02111, USA
    • Tufts Medical Center Cancer Center, Tufts University, Boston, MA 02111, USA
    • Corresponding Author InformationCorresponding author. Human Nutrition Research Center on Aging, Tufts University, Boston, MA 02111, USA. Fax: +1 617 556 3234.
  • ,
  • Ryan S. Brooks

      Affiliations

    • Vitamins and Carcinogenesis Laboratory, Jean Mayer USDA Human Nutrition Research Center on Aging, Tufts University, Boston, MA 02111, USA
  • ,
  • Eric D. Ciappio

      Affiliations

    • Vitamins and Carcinogenesis Laboratory, Jean Mayer USDA Human Nutrition Research Center on Aging, Tufts University, Boston, MA 02111, USA
    • Friedman School of Nutrition Science and Policy, Tufts University, Boston, MA 02111, USA
  • ,
  • Susan J. Kim

      Affiliations

    • Tufts Medical Center Cancer Center, Tufts University, Boston, MA 02111, USA
  • ,
  • Jimmy W. Crott

      Affiliations

    • Vitamins and Carcinogenesis Laboratory, Jean Mayer USDA Human Nutrition Research Center on Aging, Tufts University, Boston, MA 02111, USA
    • Friedman School of Nutrition Science and Policy, Tufts University, Boston, MA 02111, USA
    • Tufts Medical Center Cancer Center, Tufts University, Boston, MA 02111, USA
  • ,
  • Grace Bennett

      Affiliations

    • Obesity and Metabolism Laboratory, Jean Mayer USDA Human Nutrition Research Center on Aging, Tufts University, Boston, MA 02111, USA
    • Friedman School of Nutrition Science and Policy, Tufts University, Boston, MA 02111, USA
  • ,
  • Andrew S. Greenberg

      Affiliations

    • Obesity and Metabolism Laboratory, Jean Mayer USDA Human Nutrition Research Center on Aging, Tufts University, Boston, MA 02111, USA
    • Friedman School of Nutrition Science and Policy, Tufts University, Boston, MA 02111, USA
  • ,
  • Joel B. Mason

      Affiliations

    • Vitamins and Carcinogenesis Laboratory, Jean Mayer USDA Human Nutrition Research Center on Aging, Tufts University, Boston, MA 02111, USA
    • Friedman School of Nutrition Science and Policy, Tufts University, Boston, MA 02111, USA
    • Tufts Medical Center Cancer Center, Tufts University, Boston, MA 02111, USA
    • Division of Gastroenterology, Tufts Medical Center, Tufts University, Boston, MA 02111, USA

Received 21 March 2011; received in revised form 28 June 2011; accepted 8 July 2011. published online 03 January 2012.
Corrected Proof

Abstract 

Inflammation associated with obesity may play a role in colorectal carcinogenesis, but the underlying mechanism remains unclear. This study investigated whether the Wnt pathway, an intracellular signaling cascade that plays a critical role in colorectal carcinogenesis, is activated by obesity-induced elevation of the inflammatory cytokine tumor necrosis factor-alpha (TNF-α). Animal studies were conducted on C57BL/6 mice, and obesity was induced by utilizing a high-fat diet (60% kcal). An inflammation-specific microarray was performed, and results were confirmed with real-time polymerase chain reaction. The array revealed that diet-induced obesity increased the expression of TNF-α in the colon by 72% (P=.004) and that of interleukin-18 by 41% (P=.023). The concentration of colonic TNF-α protein, determined by ex vivo culture assay, was nearly doubled in the obese animals (P=.002). The phosphorylation of glycogen synthase kinase 3 beta (GSK3β), an important intermediary inhibitor of Wnt signaling and a potential target of TNF-α, was quantitated by immunohistochemistry. The inactivated (phosphorylated) form of GSK3β was elevated in the colonic mucosa of obese mice (P<.02). Moreover, β-catenin, the key effector of canonical Wnt signaling, was elevated in the colons of obese mice (P<.05), as was the expression of a downstream target gene, c-myc (P<.05). These data demonstrate that diet-induced obesity produces an elevation in colonic TNF-α and instigates a number of alterations of key components within the Wnt signaling pathway that are protransformational in nature. Thus, these observations offer evidence for a biologically plausible avenue, the Wnt pathway, by which obesity increases the risk of colorectal cancer.

Abbreviations: TNF-α, tumor necrosis factor-alpha, Apc, adenomatous polyposis coli, GSK3β, glycogen synthase kinase 3 beta

Keywords: Obesity, TNF-α, Wnt pathway, Colon cancer

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 All authors do not have any conflict of interest.

PII: S0955-2863(11)00218-X

doi:10.1016/j.jnutbio.2011.07.002

« BackThe Journal of Nutritional Biochemistry