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间歇性热量限制与二十碳五烯酸联合抑制乳腺肿瘤。

Combination of intermittent calorie restriction and eicosapentaenoic acid for inhibition of mammary tumors.

机构信息

University of Minnesota, Hormel Institute, 801 16th Ave. NE, Austin, MN 55912, USA.

出版信息

Cancer Prev Res (Phila). 2013 Jun;6(6):540-7. doi: 10.1158/1940-6207.CAPR-13-0033. Epub 2013 Apr 2.

Abstract

There are a number of dietary interventions capable of inhibiting mammary tumorigenesis; however, the effectiveness of dietary combinations is largely unexplored. Here, we combined 2 interventions previously shown individually to inhibit mammary tumor development. The first was the use of the omega-3 fatty acid, eicosapentaenoic acid (EPA), and the second was the implementation of calorie restriction. MMTV-Her2/neu mice were used as a model for human breast cancers, which overexpress Her2/neu. Six groups of mice were enrolled. Half were fed a control (Con) diet with 10.1% fat calories from soy oil, whereas the other half consumed a diet with 72% fat calories from EPA. Within each diet, mice were further divided into ad libitum (AL), chronic calorie-restricted (CCR), or intermittent calorie-restricted (ICR) groups. Mammary tumor incidence was lowest in ICR-EPA (15%) and highest in AL-Con mice (87%), whereas AL-EPA, CCR-Con, CCR-EPA, and ICR-Con groups had mammary tumor incidence rates of 63%, 47%, 40%, and 59%, respectively. Survival was effected similarly by the interventions. Consumption of EPA dramatically reduced serum leptin (P < 0.02) and increased serum adiponectin in the AL-EPA mice compared with AL-Con mice (P < 0.001). Both CCR and ICR decreased serum leptin and insulin-like growth factor I (IGF-I) compared with AL mice but not compared with each other. These results illustrate that mammary tumor inhibition is significantly increased when ICR and EPA are combined as compared with either intervention alone. This response may be related to alterations in the balance of serum growth factors and adipokines.

摘要

有许多饮食干预措施能够抑制乳腺癌的发生;然而,饮食组合的有效性在很大程度上尚未得到探索。在这里,我们将两种已被证明能够单独抑制乳腺肿瘤发生的干预措施结合起来。第一种是使用ω-3 脂肪酸二十碳五烯酸(EPA),第二种是实施热量限制。MMTV-Her2/neu 小鼠被用作人类乳腺癌的模型,该模型过度表达 Her2/neu。共招募了六组小鼠。一半小鼠喂食对照(Con)饮食,其中 10.1%的脂肪热量来自豆油,而另一半则喂食含有 72%脂肪热量的 EPA 饮食。在每种饮食中,小鼠进一步分为自由进食(AL)、慢性热量限制(CCR)或间歇性热量限制(ICR)组。ICR-EPA 组的乳腺肿瘤发生率最低(15%),AL-Con 组最高(87%),而 AL-EPA、CCR-Con、CCR-EPA 和 ICR-Con 组的乳腺肿瘤发生率分别为 63%、47%、40%和 59%。干预措施对生存也有类似的影响。与 AL-Con 组相比,EPA 的摄入使 AL-EPA 组的血清瘦素显著降低(P<0.02),血清脂联素显著增加(P<0.001)。与 AL 组相比,CCR 和 ICR 均降低了血清瘦素和胰岛素样生长因子 I(IGF-I),但彼此之间没有差异。这些结果表明,与单独使用任一干预措施相比,ICR 和 EPA 的联合使用显著增加了对乳腺肿瘤的抑制作用。这种反应可能与血清生长因子和脂肪因子平衡的改变有关。

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本文引用的文献

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The insulin-like growth factor system in cancer.癌症中的胰岛素样生长因子系统。
Endocrinol Metab Clin North Am. 2012 Jun;41(2):335-50, vi. doi: 10.1016/j.ecl.2012.04.014.
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