Integrated Microbiota and Metabolite Changes following Rice Bran Intake during Murine Inflammatory Colitis-Associated Colon Cancer and in Colorectal Cancer Survivors

Author:

Weber Annika M.1ORCID,Ibrahim Hend23ORCID,Baxter Bridget A.3,Kumar Robin4ORCID,Maurya Akhilendra K.5ORCID,Kumar Dileep5ORCID,Agarwal Rajesh5ORCID,Raina Komal45ORCID,Ryan Elizabeth P.3ORCID

Affiliation:

1. Department of Food Science and Human Nutrition, Colorado State University, Fort Collins, CO 80523, USA

2. Department of Medical Biochemistry, Faculty of Medicine, Zagazig University, Zagazig 44519, Egypt

3. Department of Environmental and Radiological Health Sciences, Colorado State University, Fort Collins, CO 80523, USA

4. Department of Pharmaceutical Sciences, South Dakota State University, Brookings, SD 57007, USA

5. Department of Pharmaceutical Sciences, University of Colorado Denver—Anschutz Medical Campus, Aurora, CO 80045, USA

Abstract

Dietary rice bran-mediated inhibition of colon carcinogenesis was demonstrated previously for carcinogen-induced rodent models via multiple anti-cancer mechanisms. This study investigated the role of dietary rice bran-mediated changes to fecal microbiota and metabolites over the time course of colon carcinogenesis and compared murine fecal metabolites to human stool metabolic profiles following rice bran consumption by colorectal cancer survivors (NCT01929122). Forty adult male BALB/c mice were subjected to azoxymethane (AOM)/dextran sodium sulfate (DSS)-induced colitis-associated colon carcinogenesis and randomized to control AIN93M (n = 20) or diets containing 10% w/w heat-stabilized rice bran (n = 20). Feces were serially collected for 16S rRNA amplicon sequencing and non-targeted metabolomics. Fecal microbiota richness and diversity was increased in mice and humans with dietary rice bran treatment. Key drivers of differential bacterial abundances from rice bran intake in mice included Akkermansia, Lactococcus, Lachnospiraceae, and Eubacterium xylanophilum. Murine fecal metabolomics revealed 592 biochemical identities with notable changes to fatty acids, phenolics, and vitamins. Monoacylglycerols, dihydroferulate, 2-hydroxyhippurate (salicylurate), ferulic acid 4-sulfate, and vitamin B6 and E isomers significantly differed between rice bran- and control-fed mice. The kinetics of murine metabolic changes by the host and gut microbiome following rice bran consumption complemented changes observed in humans for apigenin, N-acetylhistamine, and ethylmalonate in feces. Increased enterolactone abundance is a novel diet-driven microbial metabolite fecal biomarker following rice bran consumption in mice and humans from this study. Dietary rice bran bioactivity via gut microbiome metabolism in mice and humans contributes to protection against colorectal cancer. The findings from this study provide compelling support for rice bran in clinical and public health guidelines for colorectal cancer prevention and control.

Funder

NIH-National Cancer Institute

National Institute of Allergy and Infectious Diseases of the National Institutes of Health

Publisher

MDPI AG

Subject

Cancer Research,Oncology

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