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

Oncotarget. 2016 Oct 4;7(40):65669-65675. doi: 10.18632/oncotarget.11598.

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.

Keywords: Lewis lung carcinoma; energy restriction; high-fat diet; metastasis; mice.

MeSH terms

  • Animals
  • Caloric Restriction*
  • Carcinoma, Lewis Lung / etiology
  • Carcinoma, Lewis Lung / pathology
  • Carcinoma, Lewis Lung / prevention & control*
  • Diet*
  • Diet, High-Fat / adverse effects*
  • Energy Intake*
  • Lung Neoplasms / etiology
  • Lung Neoplasms / prevention & control*
  • Lung Neoplasms / secondary
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Mice, Nude