Plum polyphenols inhibit colorectal aberrant crypt foci formation in rats: potential role of the miR-143/protein kinase B/mammalian target of rapamycin axis

被引:26
作者
Banerjee, Nivedita [1 ]
Kim, Hyemee [2 ]
Talcott, Stephen T. [2 ]
Turner, Nancy D. [1 ,2 ]
Byrne, David H. [3 ]
Mertens-Talcott, Susanne U. [2 ,4 ]
机构
[1] Texas A&M Univ, Interdisciplinary Program Toxicol, College Stn, TX 77843 USA
[2] Texas A&M Univ, Dept Nutr & Food Sci, College Stn, TX 77843 USA
[3] Texas A&M Univ, Dept Hort, College Stn, TX 77843 USA
[4] Texas A&M Univ, Dept Vet Physiol & Pharmacol, College Stn, TX 77843 USA
关键词
Plum; Chlorogenic acid; Colon cancer; Inflammation; mTOR; miR-143; Rat; CANCER-CELLS; COLON CARCINOGENESIS; OXIDATIVE STRESS; CHLOROGENIC ACID; FERULIC ACID; SIGNALING PATHWAY; MAMMALIAN TARGET; UP-REGULATION; INFLAMMATION; GROWTH;
D O I
10.1016/j.nutres.2016.06.008
中图分类号
R15 [营养卫生、食品卫生]; TS201 [基础科学];
学科分类号
100403 ;
摘要
The nutritional prevention of aberrant crypt foci by polyphenols may be a crucial step to dietary cancer prevention. The objective of this study was to determine the underlying mechanisms that contribute to the anti-inflammatory and antitumorigenic properties of plum (Prunus salicina L.) polyphenols, including chlorogenic acid and neochlorogenic acid, in azoxymethane (AOM)-treated rats. The hypothesis was that plum polyphenolics suppress AOM-induced aberrant crypt foci formation through alterations in the protein kinase B (AKT)/mammalian target of rapamycin (mTOR) pathway and relative micro-RNA expressions. Sprague-Dawley rats (n = 10/group) received plum beverage (1346 mg gallic acid equivalents/L) or a control beverage ad libitum for 10 weeks with subcutaneous injections of AOM (15 mg/kg) at weeks 2 and 3. Results show that the consumption of the plum beverage decreased the number of dysplastic aberrant crypt foci by 48% (P < .05) and lowered proliferation of mucosal cells by 24% (P < .05). The plum beverage decreased the activity of glutathione peroxidase, superoxide dismutase, and catalase in mucosal scrapings, as well as the superoxide dismutase activity in serum. The results were accompanied by a down-regulation of proinflammatory enzymes nuclear factor kappa B, nitric oxide synthase, cyclooxygenase-2, and vascular cell adhesion molecule 1 messenger RNA. Plum inhibited the expression of AKT and mTOR messenger RNA, phosphorylated AKT, mTOR, and hypoxiainducible factor-la protein levels, and the ratio of the phosphorylated/total protein expression of mTOR. Also, the plum beverage increased the expression of miR-143, which is involved in the regulation of AKT. These results suggest that plum polyphenols may exhibit a chemopreventive potential against colon carcinogenesis by impacting the AKT/mTOR pathway and miR-143. (C) 2016 Elsevier Inc. All rights reserved.
引用
收藏
页码:1105 / 1113
页数:9
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