Dietary Manipulation of Oncogenic MicroRNA Expression in Human Rectal Mucosa: A Randomized Trial

被引:82
作者
Humphreys, Karen J. [1 ]
Conlon, Michael A. [2 ,3 ]
Young, Graeme P. [1 ]
Topping, David L. [2 ,3 ]
Hu, Ying [1 ]
Winter, Jean M. [1 ]
Bird, Anthony R. [2 ,3 ]
Cobiac, Lynne [2 ,3 ]
Kennedy, Nicholas A. [4 ]
Michael, Michael Z. [1 ]
Le Leu, Richard K. [2 ,3 ]
机构
[1] Flinders Univ S Australia, Sch Med, Flinders Ctr Innovat Canc, Flinders Med Ctr, Adelaide, SA 5042, Australia
[2] CSIRO, Preventat Hlth Natl Res Flagship, Adelaide, SA, Australia
[3] CSIRO Anim Food & Hlth Sci, Adelaide, SA, Australia
[4] Flinders Med Ctr, Dept Gastroenterol, Adelaide, SA, Australia
基金
英国医学研究理事会;
关键词
CHAIN FATTY-ACIDS; RESISTANT STARCH; RED MEAT; BUTYRYLATED STARCH; GENE-EXPRESSION; DNA-DAMAGE; BUTYRATE; COLON; TRICHOSTATIN; FERMENTATION;
D O I
10.1158/1940-6207.CAPR-14-0053
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
High red meat (HRM) intake is associated with increased colorectal cancer risk, while resistant starch is probably protective. Resistant starch fermentation produces butyrate, which can alter microRNA (miRNA) levels in colorectal cancer cells in vitro; effects of red meat and resistant starch on miRNA expression in vivo were unknown. This study examined whether a HRM diet altered miRNA expression in rectal mucosa tissue of healthy volunteers, and if supplementation with butyrylated resistant starch (HRM+HAMSB) modified this response. In a randomized cross-over design, 23 volunteers undertook four 4-week dietary interventions; an HRM diet (300 g/day lean red meat) and an HRM+HAMSB diet (HRM with 40 g/day butyrylated high amylose maize starch), preceded by an entry diet and separated by a washout. Fecal butyrate increased with the HRM+HAMSB diet. Levels of oncogenic mature miRNAs, including miR17-92 cluster miRNAs and miR21, increased in the rectal mucosa with the HRM diet, whereas the HRM+HAMSB diet restored miR17-92 miRNAs, but not miR21, to baseline levels. Elevated miR17-92 and miR21 in the HRM diet corresponded with increased cell proliferation, and a decrease in miR17-92 target gene transcript levels, including CDKN1A. The oncogenic miR17-92 cluster is differentially regulated by dietary factors that increase or decrease risk for colorectal cancer, and this may explain, at least in part, the respective risk profiles of HRM and resistant starch. These findings support increased resistant starch consumption as a means of reducing risk associated with an HRM diet. (C)2014 AACR.
引用
收藏
页码:786 / 795
页数:10
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