Effect of Caloric Intake on Western-Style Diet-Induced Intestinal Tumors in a Mouse Model for Hereditary Colon Cancer

被引:4
|
作者
Itano, Osamu [1 ]
Fan, Kunhua [1 ]
Yang, Kan [1 ]
Suzuki, Keiich [1 ]
Quimby, Fred [2 ]
Dong, Zhiqian [1 ]
Jin, Bo [3 ]
Edelmann, Winfried [3 ]
Lipkin, Martin [1 ]
机构
[1] Weill Cornell Med Coll, Dept Med Gastroenterol & Hepatol, New York, NY 10021 USA
[2] Rockefeller Univ, Lab Anim Res Ctr, New York, NY 10021 USA
[3] Albert Einstein Coll Med, Dept Cell Biol, Bronx, NY 10467 USA
来源
NUTRITION AND CANCER-AN INTERNATIONAL JOURNAL | 2012年 / 64卷 / 03期
基金
美国国家卫生研究院;
关键词
FAMILIAL ADENOMATOUS POLYPOSIS; ABERRANT CRYPT FOCI; ENERGY RESTRICTION; COLORECTAL-CANCER; CELL-PROLIFERATION; WEIGHT-LOSS; VITAMIN-D; SKIN CARCINOGENESIS; FAT; GROWTH;
D O I
10.1080/01635581.2012.660672
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Increased caloric intake has been associated with increased risk for cancer of the large intestine. We studied caloric intake effect on tumor formation in Apc1638(N/+) mice, a preclinical model for human familial adenomatous polyposis. Mice were fed a controlled AIN-76A diet or a new Western-style diet (NWD). Intestinal tumor development was evaluated after 6 mu of feeding 1) AIN-76A diet (fed ad libitum) vs. AIN-76A (caloric intake reduced 30%); 2) NWD (led ad libitum) vs. NWD (caloric intake reduced 30%); and 3) AIN-76A (fed ad libitum) vs. NWD (paired-fed with NWD providing equal caloric intakes to AIN-76A). Intestinal tumor incidences were 78-100% with intergroup variation P > 0.05; however, tumor multiplicity responded differently to dietary treatment: 1) Tumor multiplicity was unchanged after AIN-76A (caloric intake reduced 30% vs. mice fed AIN-76A ad libitum); 2) tumor multiplicity was unchanged after NWD (caloric intake reduced 30% vs. NWD ad libitum); and 3) tumor multiplicity increased 130% after NWD was paired-fed with the same caloric intake as mice fed AIN-76A ad libitum (P < 0.05). Body weights showed no association with tumor development. Findings indicated modified nutrients in NWD were mainly responsible for increased tumors in mice fed NWD vs. AIN-76A in this preclinical mouse model for human FAP.
引用
收藏
页码:401 / 408
页数:8
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