Dietary energy restriction reduces high-fat diet-enhanced metastasis of Lewis lung carcinoma in mice

被引:14
|
作者
Sundaram, Sneha [1 ]
Yan, Lin [1 ]
机构
[1] ARS, USDA, Grand Forks Human Nutr Res Ctr, Grand Forks, ND 58202 USA
关键词
energy restriction; high-fat diet; Lewis lung carcinoma; metastasis; mice; TUMOR-GROWTH; PROSTATE-CANCER; WEIGHT-LOSS; OBESITY; OVERWEIGHT; INFLAMMATION; RECURRENCE; EXERCISE; IMPACT;
D O I
10.18632/oncotarget.11598
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The objective of this study was to determine whether a reduction in energy intake ameliorated the high-fat diet-enhanced spontaneous metastasis of Lewis lung carcinoma in mice. Male C57BL/6 mice were fed the AIN93G diet, a high-fat diet or a high-fat diet with a 5% restriction of the intake. Energy restriction reduced body adiposity and body weight, but maintained growth similar to mice fed the AIN93G diet. The high-fat diet significantly increased the number and size (cross-sectional area and volume) of metastases formed in lungs. Restricted feeding reduced the number of metastases by 23%, metastatic cross-sectional area by 32% and volume by 45% compared to the high-fat diet. The high-fat diet elevated plasma concentrations of proinflammatory cytokines (monocyte chemotactic protein-1, plasminogen activator inhibitor-1, leptin), angiogenic factors (vascular endothelial growth factor, tissue inhibitor of metalloproteinase-1) and insulin. Restricted feeding significantly reduced the high-fat diet-induced elevations in plasma concentrations of proinflammatory cytokines, angiogenic factors and insulin. These results demonstrated that a reduction in diet intake by 5% reduced high-fat diet-enhanced metastasis, which may be associated with the mitigation of adiposity and down-regulation of cancer-promoting proinflammatory cytokines and angiogenic factors.
引用
收藏
页码:65669 / 65675
页数:7
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