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TitleCombined inadequacies of multiple B vitamins amplify colonic Wnt signaling and promote intestinal tumorigenesis in BAT-LacZxApc1638N mice
Publication TypeJournal Article
Year of Publication2011
AuthorsLiu Z, Ciappio ED, Crott JW, Brooks RS, Nesvet J, Smith DE, Choi {S-W}, Mason JB
JournalThe FASEB Journal: Official Publication of the Federation of American Societies for Experimental Biology
Volume25
Pagination3136–3145
ISSN1530-6860
KeywordsAnimals, Apoptosis, Cell Cycle, Cell Proliferation, Colon, Colorectal Neoplasms, diet, Epithelial Cells, Gene Expression Regulation, Genes, Intestinal Mucosa, Lac Operon, Mice, Reporter, Signal Transduction, Vitamin B Deficiency, Wnt Proteins
Abstract

The Wnt pathway is a pivotal signaling cascade in colorectal carcinogenesis. The purpose of this work is to determine whether depletion of folate and other metabolically related B vitamins induces in vivo activation of intestinal Wnt signaling and whether this occurs in parallel with increased tumorigenesis. A hybrid mouse was created by crossing a Wnt-reporter animal (BAT-LacZ) with a model of colorectal cancer (Apc1638N). A mild depletion of folate and vitamins B₂, B₆, and B₁₂ was induced over 16 wk, and the control animals in each instance were pair fed a diet containing the basal requirement of these nutrients. The multiplicity of macroscopic tumors and aberrant crypt foci both increased by {\textasciitilde}50% in the hybrid mice fed the depletion diet (P<0.05). A 4-fold elevation in Wnt signaling was produced by the depletion diet (P<0.05) and was accompanied by significant changes in the expression of a number of Wnt-related genes in a pattern consistent with its activation. Proliferation and apoptosis of the colonic mucosa both changed in a protransformational direction (P<0.05). In summary, mild depletion of multiple B vitamins produces in vivo activation of colonic Wnt signaling, implicating it as a key pathway by which B-vitamin inadequacies enhance intestinal tumorigenesis.

URLhttp://www.ncbi.nlm.nih.gov/pubmed/21646397
DOI10.1096/fj.11-184143