Chitosan oligosaccharide suppresses tumor progression in a mouse model of colitis-associated colorectal cancer through AMPK activation and suppression of NF-κB and mTOR signaling

被引:89
作者
Mattaveewong, Tharinee [1 ]
Wongkrasant, Preedajit [1 ]
Chanchai, Sumalee [2 ]
Pichyangkura, Rath [3 ]
Chatsudthipong, Varanuj [1 ,4 ,5 ]
Muanprasat, Chatchai [1 ,4 ,5 ]
机构
[1] Mahidol Univ, Fac Sci, Dept Physiol, Rama 6 Rd, Bangkok 10400, Thailand
[2] Mahidol Univ, Fac Sci, Dept Anat, Bangkok 10400, Thailand
[3] Chulalongkorn Univ, Fac Sci, Dept Biochem, Bangkok 10330, Thailand
[4] TCELS, ECDD, Bangkok 10400, Thailand
[5] Minist Educ, Ctr Excellence Med Biotechnol, Bangkok 10400, Thailand
关键词
Colorectal cancer; Chemoprevention; Chitosan oligosaccharide; AMP-activated protein kinase; PROTEIN-KINASE; PROGNOSTIC-SIGNIFICANCE; CARCINOGENESIS; PROLIFERATION; PREVENTION; EXPRESSION; METFORMIN; MECHANISM; ASPIRIN; THERAPY;
D O I
10.1016/j.carbpol.2016.02.077
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
Novel, effective and safe agents are needed for the chemoprevention of colorectal cancer (CRC). This study investigated the effects of chitosan oligosaccharides (COS) on CRC progression and their underlying mechanisms and safety profiles in mice. Using a mouse model of colitis-associated CRC, we found that oral administration of COS (500 mg/kg/day) resulted in a similar to 60% reduction of tumor size and tumor numbers/sectioning. In addition, COS treatment increased AMPK activity, suppressed the NF-kappa B-mediated inflammatory response and reduced the expressions of cyclin D1, phosphorylated ribosomal protein S6, and MMP-9 in the colon tissues of these mice. Importantly, administration of COS (500 mg/kg/day; 50 days) had no adverse effects on renal or liver functions. Our results indicate that COS suppressed CRC progression via AMPK activation and the suppression of NF-kappa B and mTOR signaling. COS may be of potential utility in the chemoprevention of CRC. (C) 2016 Elsevier Ltd. All rights reserved.
引用
收藏
页码:30 / 36
页数:7
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