Black raspberries suppress colonic adenoma development in ApcMin/+ mice: Relation to metabolite profiles

Pan Pan, Chad W. Skaer, Hsin Tzu Wang, Steven M. Stirdivant, Matthew R. Young, Kiyoko Oshima, Gary D. Stoner, John F. Lechner, Yi Wen Huang, Li Shu Wang

Research output: Contribution to journalArticlepeer-review

Abstract

Freeze-dried black raspberries (BRBs) have demonstrated chemopreventive effects in a dietary intervention trial with human colorectal cancer patients. The aim of this study was to investigate BRB-caused metabolite changes using the ApcMin/+ mouse as a model of human colorectal cancer. Wild-type (WT) mice were fed control diet, and ApcMin/+ mice were fed either control diet or control diet supplemented with 5% BRBs for 8 weeks. Colonic and intestinal polyp size and number were measured. A non-targeted metabolomic analysis was conducted on colonic mucosa, liver and fecal specimens. Eight weeks of BRB treatment significantly decreased intestinal and colonic polyp number and size in ApcMin/+ mice. The apc gene mutation significantly changed 52 metabolites in colonic mucosa associated with increased amino acid and decreased lipid metabolites, as well as 39 liver and 8 fecal metabolites. BRBs significantly reversed 23 apc-regulated metabolites, including 13 colonic mucosa, 8 liver and 2 fecal metabolites that were involved in amino acid, glutathione, lipid and nucleotide metabolism. Of these, changes in eight metabolites were linearly correlated with decreased colonic polyp number and size in BRB-treated ApcMin/+ mice. Elevated levels of putrescine and linolenate in ApcMin/+ mice were significantly decreased by BRBs. Ornithine decarboxylase expression, the key enzyme in putrescine generation, was fully suppressed by BRBs. These results suggest that BRBs produced beneficial effects against colonic adenoma development in ApcMin/+ mice and modulated multiple metabolic pathways. The metabolite changes produced by BRBs might potentially reflect the BRB-mediated chemopreventive effects in colorectal cancer patients.

Original languageEnglish (US)
Article numberbgv107
Pages (from-to)1245-1253
Number of pages9
JournalCarcinogenesis
Volume36
Issue number10
DOIs
StatePublished - Aug 16 2015
Externally publishedYes

ASJC Scopus subject areas

  • Cancer Research

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