Anthocyanin-rich red grape extract impedes adenoma development in the ApcMin mouse: Pharmacodynamic changes and anthocyanin levels in the murine biophase

被引:21
作者
Cai, Hong
Marczylo, Timothy H.
Teller, Nicole [2 ,3 ]
Brown, Karen
Steward, William P.
Marko, Doris [2 ,3 ]
Gescher, Andreas J. [1 ]
机构
[1] Univ Leicester, RKCSB, Dept Canc Studies & Mol Med, Canc Biomarkers & Prevent Grp, Leicester LE2 7LX, Leics, England
[2] Univ Vienna, Inst Analyt Chem & Food Chem, A-1010 Vienna, Austria
[3] Univ Karlsruhe, Sect Food Toxicol, Inst Appl Biosci, Karlsruhe, Germany
关键词
Anthocyanins; Chemoprevention; Drug development; BLACK-RASPBERRIES; CANCER; CARCINOGENESIS; TUMORIGENESIS; DELPHINIDIN; SUPPRESSION; MODEL; COLOR;
D O I
10.1016/j.ejca.2009.12.017
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose: Red grape pomace extract (oenocyanin) is a cheap and rich source of anthocyanins, the agents suggested to possess cancer chemopreventive properties. Here the hypothesis was tested that oenocyanin added to the diet can interfere with intestinal adenoma development in the Apc(Min) mouse, a model of intestinal carcinogenesis linked to an Apc mutation. Methods: Mice received oenocyanin (0.3%) in their diet until week 16, when adenoma number and burden were recorded. Expression of Akt and ERK proteins was studied by Western blot in adenomas to discover effects of anthocyanins on cellular signalling via the P13 and MAP kinase pathways. Levels of anthocyanins were measured by HPLC with visible spectroscopic or mass spectrometric detection. Results: In mice which had consumed oenocyanin, overall adenoma burden was halved and adenoma number was marginally reduced when compared with mice on control diet. The proliferation index in colonic adenomatous crypts, as reflected by Ki-67 staining, was significantly decreased from 88.14% in control mice to 75.6 +/- 4% in mice on oenocyanin (P = 0.014). Expression of Akt in small intestinal adenomas from Apc(Min) mice on oenocyanin was reduced by 54% (P = 0.003), when compared to controls. Oenocyanin anthocyanins and glucuronide metabolites were found in the urine and intestine but not in plasma. Conclusions: The results suggest that oenocyanin may be a viable and economical alternative to anthocyanin-rich berry extracts for chemopreventive intervention. Akt and pErk might be suitable biomarkers of anthocyanin target organ efficacy. (C) 2009 Elsevier Ltd. All rights reserved.
引用
收藏
页码:811 / 817
页数:7
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