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Development of hepatocellular cancer induced by long term low fat-high carbohydrate diet in a NAFLD/NASH mouse model

机译:长期低脂高碳水化合物饮食在NAFLD / NASH小鼠模型中诱发的肝细胞癌的发展

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摘要

Nonalcoholic fatty liver disease (NAFLD) is a common chronic liver disease. It can progress to nonalcoholic steatohepatitis (NASH) and, in a percentage of cases, to hepatocarcinogenesis. The strong incidence in western countries of obesity and metabolic syndrome, whose NAFLD is the hepatic expression, is thought to be correlated to consumption of diets characterized by processed food and sweet beverages. Previous studies described high-fat diet-induced liver tumors. Conversely, the involvement of low-fat/high-carbohydrate diet in the progression of liver disease or cancer initiation has not been described yet. Here we show for the first time hepatic cancer formation in low-fat/high-carbohydrate diet fed NAFLD/NASH mouse model. Animals were long term high-fat, low-fat/high-carbohydrate or standard diet fed. We observed progressive liver damage in low-fat/high-carbohydrate and high-fat animals after 12 and, more, 18 months. Tumors were detected in 20% and 50% of high-fat diet fed mice after 12 and 18 months and, interestingly, in 30% of low-fat/high-carbohydrate fed animals after 18 months. No tumors were detected in standard diet fed mice. Global increase of hepatic interleukin-1β, interleukin-6, tumor necrosis factor-α and hepatocyte growth factor was detected in low-fat/high-carbohydrate and high-fat with respect to standard diet fed mice as well as in tumor with respect to non-tumor bearing mice. A panel of 15 microRNAs was analyzed: some of them revealed differential expression in low-fat/high-carbohydrate with respect to high-fat diet fed groups and in tumors. Data here shown provide the first evidence of the involvement of low-fat/high-carbohydrate diet in hepatic damage leading to tumorigenesis.
机译:非酒精性脂肪肝病(NAFLD)是一种常见的慢性肝病。它可以发展为非酒精性脂肪性肝炎(NASH),在某些情况下还可以发展为肝癌发生。西方国家肥胖和代谢综合症的发生率很高,其NAFLD是肝表达,据认为与食用以加工食品和甜饮料为特征的饮食有关。先前的研究描述了高脂饮食诱导的肝肿瘤。相反,还没有描述低脂/高碳水化合物饮食与肝脏疾病或癌症发病进程的关系。在这里,我们首次显示低脂/高碳水化合物饮食喂养的NAFLD / NASH小鼠模型中的肝癌形成。长期饲喂高脂,低脂/高碳水化合物或标准饮食的动物。我们观察了低脂/高碳水化合物和高脂动物在12个月甚至18个月后进行性肝损害。在12和18个月后,高脂饮食喂养的小鼠中有20%和50%检测到肿瘤,而在18个月后,低脂/高碳水化合物喂养的动物中有30%发现了肿瘤。在标准饮食喂养的小鼠中未检测到肿瘤。在低脂/高碳水化合物和高脂饮食中,相对于标准饮食喂养的小鼠以及在肿瘤中,检测到肝白细胞介素-1β,白介素-6,肿瘤坏死因子-α和肝细胞生长因子的总体增加非荷瘤小鼠。分析了一组15种microRNA:其中一些揭示相对于高脂饮食喂养组和肿瘤在低脂/高碳水化合物中的差异表达。这里显示的数据提供了低脂/高碳水化合物饮食参与导致肿瘤发生的肝损害的第一个证据。

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