Bamboo Salt Suppresses Colon Carcinogenesis in C57BL/6 Mice with Chemically Induced Colitis

被引:10
|
作者
Ju, Jaehyun [1 ,2 ]
Lee, Ga-Young [1 ]
Kim, Yoon-Se [3 ]
Chang, Hee Kyung [4 ]
Do, Myoung-Sool [5 ]
Park, Kun-Young [1 ,2 ,6 ]
机构
[1] Pusan Natl Univ, Dept Food Sci & Nutr, Busan, South Korea
[2] Cha Univ, Dept Food Sci & Biotechnol, Seongnam 13488, South Korea
[3] Insanga Co, Hamyang, South Korea
[4] Kosin Univ, Dept Pathol, Coll Med, Busan, South Korea
[5] Handong Global Univ, Sch Life Sci, Pohang, South Korea
[6] Chongqing Univ Educ, Chongqing Collaborat Innovat Ctr Funct Food, Chongqing, Peoples R China
关键词
azoxymethane; bamboo salt; colon cancer; dextran sodium sulfate; CANCER; INFLAMMATION; P53;
D O I
10.1089/jmf.2016.3798
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
The aim of our experiment was to evaluate the anticancer effect of bamboo salt (BS) on C57BL/6 mice in an azoxymethane (AOM)/dextran sodium sulfate (DSS)-induced colon cancer model. BS, solar salt, and purified salt were evaluated for their protective effects during AOM/DSS-induced colon carcinogenesis in C57BL/6 mice. BS, especially after baking for nine separate intervals (BS9x), suppressed colon carcinogenesis in the mice. BS9x decreased colon length shortening, weight-to-length ratios, and tumor counts. Pathological evidence from histological evaluation by hematoxylin and eosin staining also revealed suppression of tumorigenesis. BS9x lowered serum levels of proinflammatory cytokines (TNF-alpha, IL-6, and IL-1 beta) to close to those of the Normal group. Additionally, BS9x suppressed colon mRNA expression of proinflammatory factors and significantly regulated mRNA levels of the apoptosis-related factors, Bax and Bcl-2, and the cell cycle-related genes, p21 and p53. Additionally, immunohistochemistry showed that BS promoted p21 expression in the colon. Taken together, the results indicate that BS exhibited anticancer efficacy by modulating apoptosis-and inflammation-related gene expression during colon carcinogenesis in mice, and repetition in baking cycles of BS enhanced its anticancer functionality.
引用
收藏
页码:1015 / 1022
页数:8
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