Moral Raquel, Escrich Raquel, Solanas Montserrat, Vela Elena, Ruiz de Villa M Carme, Escrich Eduard
Physiology Unit, Department of Cell Biology, Physiology and Immunology, Faculty of Medicine, Universitat Autònoma de Barcelona, Bellaterra, 08193, Barcelona, Spain.
Department of Statistics, Universitat de Barcelona, 08028, Barcelona, Spain.
Eur J Nutr. 2016 Jun;55(4):1397-409. doi: 10.1007/s00394-015-0958-2. Epub 2015 Jun 20.
Nutritional factors, especially dietary lipids, may have a role in the etiology of breast cancer. We aimed to analyze the effects of high-fat diets on the susceptibility of the mammary gland to experimental malignant transformation.
Female Sprague-Dawley rats were fed a low-fat, high-corn-oil, or high-extra-virgin olive oil (EVOO) diet from weaning or from induction. Animals were induced with 7,12-dimethylbenz[a]anthracene at 53 days and euthanized at 36, 51, 100 and 246 days. Gene expression profiles of mammary glands were determined by microarrays. Further molecular analyses were performed by real-time PCR, TUNEL and immunohistochemistry. Carcinogenesis parameters were determined at 105 and 246 days.
High-corn-oil diet increased body weight and mass when administered from weaning. The EVOO diet did not modify these parameters and increased the hepatic expression of UCP2, suggesting a decrease in intake/expenditure balance. Both diets differentially modified the gene expression profile of the mammary gland, especially after short dietary intervention. Corn oil down-regulated the expression of genes related to immune system and apoptosis, whereas EVOO modified the expression of metabolism genes. Further analysis suggested an increase in proliferation and lower apoptosis in the mammary glands by effect of the high-corn-oil diet, which may be one of the mechanisms of its clear stimulating effect on carcinogenesis.
The high-corn-oil diet strongly stimulates mammary tumorigenesis in association with modifications in the expression profile and an increased proliferation/apoptosis balance of the mammary gland.
营养因素,尤其是膳食脂质,可能在乳腺癌的病因中起作用。我们旨在分析高脂饮食对乳腺实验性恶性转化易感性的影响。
雌性斯普拉格 - 道利大鼠从断奶或诱导时开始分别喂食低脂、高玉米油或高特级初榨橄榄油(EVOO)饮食。在53天时用7,12 - 二甲基苯并[a]蒽诱导动物,并在36、51、100和246天时实施安乐死。通过微阵列测定乳腺的基因表达谱。通过实时PCR、TUNEL和免疫组织化学进行进一步的分子分析。在105和246天时测定致癌参数。
从断奶开始给予高玉米油饮食会增加体重和体质量。EVOO饮食未改变这些参数,但增加了肝脏中UCP2的表达,表明摄入/消耗平衡下降。两种饮食均对乳腺的基因表达谱产生不同影响,尤其是在短期饮食干预后。玉米油下调了与免疫系统和细胞凋亡相关的基因表达,而EVOO改变了代谢基因的表达。进一步分析表明,高玉米油饮食会导致乳腺中增殖增加和细胞凋亡减少,这可能是其对致癌作用有明显刺激作用的机制之一。
高玉米油饮食与乳腺表达谱改变以及乳腺增殖/细胞凋亡平衡增加相关,强烈刺激乳腺肿瘤发生。