IL-17F deficiency inhibits small intestinal tumorigenesis in Apc Min/+ mice

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Abstract

IL-17 plays an important role in gut homeostasis. However, the role of IL-17F in intestinal tumorigenesis has not been addressed. Here we demonstrate that ablation of IL-17F significantly inhibits spontaneous intestinal tumorigenesis in the small intestine of Apc Min/+ mice. IL-17F ablation decreased IL-1β and Cox-2 expression as well as IL-17 receptor C (IL-17RC) expression, which were increased in tumors from Apc Min/+ mice. Lack of IL-17F did not reverse the splenomegaly but partially restored thymic atrophy, suggesting a local effect of IL-17F in the intestine. IL-17F deficient Apc Min/+ mice showed a significant decrease in immune cell infiltration in the lamina propria. Interestingly, the expression of IL-17A from CD4 T cells in the lamina propria remains unchanged in the absence of IL-17F. Collectively, our results suggest the proinflammatory and essential role of IL-17F to develop spontaneous intestinal tumorigenesis in Apc Min/+ mice in the presence of IL-17A. © 2011 Elsevier Inc.

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Chae, W. J., & Bothwell, A. L. M. (2011). IL-17F deficiency inhibits small intestinal tumorigenesis in Apc Min/+ mice. Biochemical and Biophysical Research Communications, 414(1), 31–36. https://doi.org/10.1016/j.bbrc.2011.09.016

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