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膳食脂肪对小鼠 Lewis 肺癌自发转移的影响。

Effects of dietary fat on spontaneous metastasis of Lewis lung carcinoma in mice.

机构信息

U.S. Department of Agriculture, Grand Forks Human Nutrition Research Center, ND 58202, USA.

出版信息

Clin Exp Metastasis. 2010 Dec;27(8):581-90. doi: 10.1007/s10585-010-9347-7. Epub 2010 Aug 10.

Abstract

The present study assessed the effects of dietary fat on spontaneous metastasis of Lewis lung carcinoma in mice. Three-week old male C57BL/6 mice were fed the AIN-93G diet or a 45% fat diet (% kcal.) for 7 weeks before they were subcutaneously injected with 2.5 × 10⁵ viable carcinoma cells. The primary tumor was resected 2 weeks later, and mice were maintained on their respective diets for an additional 2 weeks. The high-fat diet significantly increased body weight and abdominal adipose weight compared to the AIN-93G diet. Feeding mice the 45% fat diet resulted in a two-fold increase in the number of lung metastases (P < 0.05), a 35% increase in tumor cross-sectional area, and a 50% increase in tumor volume compared to mice fed the AIN-93G diet. There were no differences in plasma concentrations of TIMP-1, IL-1β, VEGF and MCP-1 in non-tumor-bearing mice fed the AIN-93G diet or the high-fat diet, but significant increases in these cytokines in tumor-bearing mice fed the AIN-93G diet compared to the non-tumor-bearing mice fed the same diet (P < 0.05 for each comparison). Further significant increases in these cytokines in tumor-bearing mice fed the 45% fat diet compared to the same tumor-bearing mice fed the AIN-93G diet (P < 0.05 for each comparison). The high-fat diet significantly increased plasma leptin and significantly decreased plasma adiponectin compared to the AIN-93G diet in both non-tumor-bearing and tumor-bearing mice. Results of the present study demonstrated that the high-fat diet enhanced spontaneous metastasis of Lewis lung carcinoma in mice and that this aggressiveness was accompanied with significant increases in plasma concentrations of angiogenic cytokines, suggesting that dietary fat affects metastasis by promoting angiogenic processes.

摘要

本研究评估了膳食脂肪对小鼠 Lewis 肺癌自发转移的影响。3 周龄雄性 C57BL/6 小鼠在皮下注射 2.5×105 个活癌细胞前,分别用 AIN-93G 饮食或 45%脂肪饮食(%热量)喂养 7 周。2 周后切除原发肿瘤,小鼠继续分别用各自饮食喂养 2 周。高脂肪饮食与 AIN-93G 饮食相比,显著增加了体重和腹部脂肪重量。与用 AIN-93G 饮食喂养的小鼠相比,用 45%脂肪饮食喂养的小鼠肺转移灶数量增加了一倍(P<0.05),肿瘤横截面积增加了 35%,肿瘤体积增加了 50%。在未荷瘤的 AIN-93G 饮食或高脂肪饮食喂养的小鼠中,TIMP-1、IL-1β、VEGF 和 MCP-1 的血浆浓度没有差异,但在 AIN-93G 饮食喂养的荷瘤小鼠中,这些细胞因子的浓度显著高于相同饮食喂养的未荷瘤小鼠(每种比较均 P<0.05)。与 AIN-93G 饮食喂养的相同荷瘤小鼠相比,用 45%脂肪饮食喂养的荷瘤小鼠中这些细胞因子的浓度进一步显著增加(每种比较均 P<0.05)。与 AIN-93G 饮食相比,高脂肪饮食在未荷瘤和荷瘤小鼠中均显著增加了血浆瘦素水平,降低了血浆脂联素水平。本研究结果表明,高脂肪饮食增强了小鼠 Lewis 肺癌的自发转移,这种侵袭性伴随着血管生成细胞因子血浆浓度的显著增加,提示膳食脂肪通过促进血管生成过程影响转移。

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