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Açaí Berries Inhibit Colon Tumorigenesis in Azoxymethane/Dextran Sulfate Sodium-Treated Mice.

Authors :
Yoon Jin Choi
Nayoung Kim
Ryoung Hee Nam
Young-Joon Surh
Yoon Jeong Choi
Dong Ho Lee
Seonmin Lee
Hye Seung Lee
Ha-Na Lee
Source :
Gut & Liver. Mar2017, Vol. 11 Issue 2, p243-252. 11p.
Publication Year :
2017

Abstract

Background/Aims: The aim of this study was to investigate the protective effect of açaí against azoxymethane (AOM)/ dextran sulfate sodium (DSS)-induced colorectal cancer development. Methods: The effect of açaí on tumorigenesis was assessed by evaluating tumor incidence, multiplicity and invasiveness in the mouse colon. The levels of myeloperoxidase (MPO) and proinflammatory cytokines (tumor necrosis factor α [TNF-α], interleukin [IL]-1β, and IL-6) were measured via enzyme-linked immunosorbent assay. Protein levels of cyclooxygenase 2 (COX-2), proliferating cell nuclear antigen (PCNA), B-cell lymphoma 2 (Bcl-2), Bcl-2-associated death promoter (Bad) and cleaved-caspase-3 were assessed by immunoblotting. Results: Administration of pellets containing 5% açaí powder reduced the incidences of both colonic adenoma and cancer (adenoma, 23.1% vs 76.9%, respectively, p=0.006; cancer, 15.4% vs 76.9%, respectively, p=0.002). In the açaí-treated mice, the MPO, TNF-α, IL-1β and IL-6 levels in the colon were significantly down-regulated. Açaí inhibited PCNA and Bcl-2 expression and increased Bad and cleaved-caspase-3 expression. In vitro studies demonstrated that açaí treatment reduced lipopolysaccharide-induced expression of TNF-α, IL-1β, IL-6 and COX-2 in murine macrophage RAW 264.7 cells. Conclusions: Açaí demonstrated protective effects against AOM/DSS-induced colon carcinogenesis, which suggests that the intake of açaí may be beneficial for the prevention of human colon cancer. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
19762283
Volume :
11
Issue :
2
Database :
Academic Search Index
Journal :
Gut & Liver
Publication Type :
Academic Journal
Accession number :
121634540
Full Text :
https://doi.org/10.5009/gnl16068