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THERAPEUTIC ACTIONS

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

Written by CYBERMED LIFE NEWS
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Download this file (Dietary energy restriction reduces high-fat diet-enhanced metastasis of Lewis lung carcinoma in mice..pdf)Dietary energy restriction reduces high-fat diet-enhanced metastasis of Lewis lung carcinoma in mice..pdf[Dietary energy restriction reduces high-fat diet-enhanced metastasis of Lewis lung carcinoma in mice.]1617 kB
Abstract Title:

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

Abstract Source:

Oncotarget. 2016 Oct 4 ;7(40):65669-65675. PMID: 27582541

Abstract Author(s):

Sneha Sundaram, Lin Yan

Article Affiliation:

Sneha Sundaram

Abstract:

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.