Targeting of key developmental pathways that regulate the normal differentiation and maturation of intestinal epithelial cells is a fundamental approach for inhibition of intestinal tumorigenesis. Important proof-of-principle has been published demonstrating that inhibition of Notch signaling in mice with a ?-secretase inhibitor can drive intestinal carcinoma cells to differentiate both in vitro and in the ApcMin mouse, in the latter case causing tumor stasis and regression. We have developed a new mouse genetic model that targets Notch signaling specifically in both the small and large intestine by eliminating the enzyme that fucosylates the Notch receptor, a step that is necessary for interaction of Notch with its ligands. This produces a dramatic phenotype in the intestine: Notch signaling is down-regulated, and there is a tremendous expansion of the goblet, Paneth and enteroendocrine secretory cell lineages in both the colon and small intestine at 4 weeks of age, paralleled by a distortion of the proliferative compartment. These mice survive and appear healthy. However, by 9 months there is a very large inflammatory response in the intestinal mucosa of 100% of the mice, and evidence for development of dysplasia and adenoma formation. These data are the first demonstration of the importance of signaling specifically through Notch receptor-ligand interaction for intestinal mucosal homeostasis. Using this mouse, our overall goals are to determine how effective Notch signaling is in inhibition of intestinal tumor formation, what the longer-term consequences of this inhibition are for intestinal homeostasis, whether strategies that employ nutrients can modulate effects of Notch inhibition, and to understand the mechanisms by which Notch regulates intestinal homeostasis and its interaction with signals from the diet.
In Aim 1, we will we will introduce the ApcMin allele into these mice to determine the efficacy of inhibition of tumor formation by the efficient inactivation of Notch and the longer term tumor suppression and changes in the mucosa caused by the down- regulation of Notch in the intestinal epithelial cells. Further, using a regulated villin-cre:er transgene, we will determine the kinetics with which mucosal lineage specific differentiation and the inflammatory response develop in these mice, and whether intestinal tumors recur with time, the efficacy of repeated rounds of Notch inactivation, and the longer term influence of this on the mucosa and health of the mice. Alternatives are described that utilize an Apc floxed mouse and the AOM model of colon tumorigenesis.
In Aim 2, we will determine how the epithelial cell and the inflammatory cell responses in these mice evolve over 9 months, especially in terms of extent of inflammation, representation of major classes of inflammatory immune cells and elaboration of cytokines and other growth factors;how this is accelerated and amplified by a western-style diet that elevates risk for intestinal tumor formation;and how vitamin D supplementation, which is both chemopreventive and anti-inflammatory, can modulate these effects. Finally, Aim 3 will assay how macrophages isolated from control mice, from mice exhibiting inflammation, and from mice in which the inflammatory response has been modified by nutritional factors influence cell growth and differentiation of mouse intestinal epithelial cells both in vitro and when implanted under the kidney capsule in vivo. These experiments will determine the efficacy of down-regulation of Notch signaling in inhibiting intestinal tumor formation and the longer term effects of such down-regulation, how the responses to Notch down regulation are modulated by important nutritional factors that influence development of human colon cancer, and cellular and molecular mechanisms by which the inflammation of the intestine can be modulated by these same nutritional factors.

Public Health Relevance

Targeting of pathways that are a key in regulating the differentiation and normal functioning of the intestinal tract is an important approach to chemoprevention of intestinal cancer. Published data has provided proof of principle that targeting such a pathway known as Notch signaling is effective in causing tumor cells to undergo differentiation into normal intestinal epithelial cells, and that this approach can inhibit intestinal tumor growth in the mouse. Thus far, however, this targeting of Notch signaling has been inefficient, may lack cell-type or pathway specificity, and longer term efficacy and side effects have not been studied due to toxicity of the drugs. Dramatic effects of inactivation of Notch signaling are seen in a new mouse genetic model that we have developed. We will use this model to determine the efficacy of efficient down- regulation of Notch signaling in preventing intestinal tumor formation in the mouse, and the longer term effects of a substantial inflammation that develops in the intestine of these mice and how this evolves with time. We will also determine how a diet that mimics aspects of the human diet that establish risk for colon cancer influences the longer term effects of targeting this pathway, and whether this can be modulated by elevating vitamin D in the diet. Finally, we will determine how certain immune cells isolated from the inflammation in the mouse intestine interact with intestinal epithelial cells to influence epithelial cell growth both in tissue culture and in the mouse as tumors, their tumor properties, and how nutritional factors affect how immune cells interact with tumor cells.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Research Project (R01)
Project #
5R01CA135561-04
Application #
8204974
Study Section
Chemo/Dietary Prevention Study Section (CDP)
Program Officer
Riscuta, Gabriela
Project Start
2009-01-01
Project End
2013-12-31
Budget Start
2012-01-01
Budget End
2012-12-31
Support Year
4
Fiscal Year
2012
Total Cost
$311,205
Indirect Cost
$73,768
Name
Montefiore Medical Center (Bronx, NY)
Department
Type
DUNS #
041581026
City
New York
State
NY
Country
United States
Zip Code
10467
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