共 50 条
Pleurotus ostreatus inhibits colitis-related colon carcinogenesis in mice
被引:18
|作者:
Jedinak, Andrej
[1
]
Dudhgaonkar, Shailesh
[1
]
Jiang, Jiahua
[1
]
Sandusky, George
[2
]
Sliva, Daniel
[1
,3
,4
]
机构:
[1] Canc Res Lab, Methodist Res Inst, Indianapolis, IN 46202 USA
[2] Indiana Univ, Simon Canc Ctr, Dept Pathol & Lab Med, Indianapolis, IN 46202 USA
[3] Indiana Univ, Simon Canc Ctr, Sch Med, Bloomington, IN 47405 USA
[4] Indiana Univ, Simon Canc Ctr, Dept Med, Indianapolis, IN 46202 USA
关键词:
colorectal cancer;
PhIP;
Pleurotus ostreatus;
INFLAMMATORY-BOWEL-DISEASE;
PLEURAN BETA-GLUCAN;
FOOD-DERIVED CARCINOGEN;
SODIUM-INDUCED COLITIS;
COLORECTAL-CANCER;
RAT COLON;
F344;
RATS;
PATHWAY;
SULFATE;
CHEMOPREVENTION;
D O I:
10.3892/ijmm_00000509
中图分类号:
R-3 [医学研究方法];
R3 [基础医学];
学科分类号:
1001 ;
摘要:
Colorectal cancer is one of the leading causes of cancer deaths in both men and women in the world. However, colon cancer can be prevented to some extent by consumption of edible natural products with chemopreventive properties. Therefore, we investigated, whether edible mushroom Pleurotus ostreatus (PO) has chemopreventive effect on inflammation-associated colon carcinogenesis induced by 2-amino-1-methyl-6-phenylimidazo[4,5-b]pyridine (PhIP) and promoted by dextran sodium sulfate (DSS). PO treatment, at both doses (100 and 500 mg/kg), significantly reduced by 50 and 78% the number of aberrant crypt foci and the multiplicity of colon neoplasms by 43 and 89%, respectively. However, incidence of colon tumors and high grade dysplasia was reduced by 50 and 63% only in the dose 500 mg/kg of PO, respectively. Colon shortening and dysplastic index was significantly reduced by PO treatment in dose-dependent manner. The immunohistochemistry of colons revealed that treatment with PO suppressed expression of cyclin D1, Ki-67, COX-2 and F4/80. In summary, our data suggest that PO may prevent inflammation-associated colon carcinogenesis with exposure to PhIP through combined modulatory mechanisms of inflammation and tumor growth via suppression of COX-2, F4/80, Ki-67 and cyclin D1 expression in mice.
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页码:643 / 650
页数:8
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