...
首页> 外文期刊>Cancer prevention research. >Early Exposure to a High Fat/High Sugar Diet Increases the Mammary Stem Cell Compartment and Mammary Tumor Risk in Female Mice
【24h】

Early Exposure to a High Fat/High Sugar Diet Increases the Mammary Stem Cell Compartment and Mammary Tumor Risk in Female Mice

机译:早期暴露于高脂肪/高糖饮食增加了母老鼠中的乳腺干细胞室和乳腺肿瘤风险

获取原文
获取原文并翻译 | 示例
   

获取外文期刊封面封底 >>

       

摘要

Obesity and alterations in metabolic programming from early diet exposures can affect the propensity to disease in later life. Through dietary manipulation, developing mouse pups were exposed to a hyperinsulinemic, hyperglycemic milieu during three developmental phases: gestation, lactation, and postweaning. Analyses showed that a postweaning high fat/high sugar (HF/HS) diet had the main negative effect on adult body weight, glucose tolerance, and insulin resistance. However, dimethylbenz[ a] anthracene (DMBA)-induced carcinogenesis revealed that animals born to a mother fed a HF/HS gestation diet, nursed by a mother on a mildly diet-restricted, low fat/low sugar diet (DR) and weaned onto a HF/HS diet (HF/DR/HF) had the highest mammary tumor incidence, while HF/HF/DR had the lowest tumor incidence. Cox proportional hazards analysis showed that a HF/HS postweaning diet doubled mammary cancer risk, and a HF/HS diet during gestation and postweaning increased risk 5.5 times. Exposure to a HF/HS diet during gestation, when combined with a postweaning DR diet, had a protective effect, reducing mammary tumor risk by 86% (HR = 0.142). Serum adipocytokine analysis revealed significant diet-dependent differences in leptin/adiponectin ratio and IGF-1. Flow cytometry analysis of cells isolated from mammary glands from a high tumor incidence group, DR/HF/HF, showed a significant increase in the size of the mammary stem cell compartment compared with a low tumor group, HF/HF/DR. These results indicate that dietary reprogramming induces an expansion of the mammary stem cell compartment during mammary development, increasing likely carcinogen targets and mammary cancer risk. (C) 2017 AACR.
机译:早期饮食暴露的代谢编程的肥胖和改变可能会影响后续生命的疾病倾向。通过膳食操作,在三个发育阶段,培养的小鼠幼崽暴露于高胰岛素血症,高血糖内部:妊娠,哺乳和断奶。分析表明,两种高脂肪/高糖(HF / HS)饮食对成年体重,葡萄糖耐量和胰岛素抵抗具有主要的负面影响。然而,二甲基苯并[A]蒽(DMBA)诱导的致癌作用揭示了向母亲发出的动物喂养HF / HS妊娠饮食,由母亲在温和的饮食限制,低脂肪/低糖饮食(DR)和断奶后护理在HF / HS饮食中(HF / DR / HF)具有最高的乳腺肿瘤发病率,而HF / HF / DR具有最低的肿瘤发病率。 Cox比例危害分析表明,HF / HS后切换饮食增加了一倍加倍乳腺癌风险,并且在妊娠期间的HF / HS饮食和后续发生的风险增加了5.5倍。在妊娠期间暴露于HF / HS饮食,当结合后切换饮食时具有保护作用,减少86%(HR = 0.142)的乳腺肿瘤风险。血清adipocytokine分析显示瘦蛋白/脂联素比和IGF-1的显着饮食依赖性差异。与高肿瘤发生率-HF / HF从高肿瘤发生率分离的细胞的流式细胞术分析,与低肿瘤组,HF / HF / DR相比,乳腺干细胞室的大小显着增加。这些结果表明,膳食重编程在乳腺发育期间诱导乳腺干细胞室的膨胀,越来越可能的致癌目标和乳腺癌风险。 (c)2017年AACR。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号