一种外源性酮酯可减缓小鼠乳腺癌和肾癌模型中的肿瘤进展。

An Exogenous Ketone Ester Slows Tumor Progression in Murine Breast and Renal Cancer Models.

作者信息

Ogbonna Henry Nnaemeka, Roberts Zachary, Godwin Nicholas, Muri Pia, Turbitt William J, Swalley Zoey N, Dempsey Francesca R, Stephens Holly R, Zhang Jianqing, Plaisance Eric P, Norian Lyse A

机构信息

Graduate Biomedical Sciences, Pathobiology, Pharmacology, and Physiology, University of Alabama at Birmingham, Birmingham, AL 35233, USA.

Undergraduate Science and Technology Honors Program, University of Alabama at Birmingham, Birmingham, AL 35233, USA.

出版信息

Cancers (Basel). 2024 Oct 4;16(19):3390. doi: 10.3390/cancers16193390.

Abstract

BACKGROUND/OBJECTIVES: Ketone esters (KEs) exhibit promise as anti-cancer agents but their impact on spontaneous metastases remains poorly understood. Although consumption of a ketogenic diet (KD) that is low in carbohydrates and high in fats can lead to KE production in vivo, the restrictive composition of KDs may diminish adherence in cancer patients.

METHODS

We investigated the effects of an exogenous ketone ester-supplemented (eKET), carbohydrate-replete diet on tumor growth, metastasis, and underlying mechanisms in orthotopic models of metastatic breast (4T1-Luc) and renal (Renca-Luc) carcinomas. Mice were randomized to diet after tumor challenge.

RESULTS

Administration of KEs did not alter tumor cell growth in vitro. However, in mice, our eKET diet increased circulating β-hydroxybutyrate and inhibited primary tumor growth and lung metastasis in both models. Body composition analysis illustrated the overall safety of eKET diet use, although it was associated with a loss of fat mass in mice with renal tumors. Immunogenetic profiling revealed divergent intratumoral eKET-related changes by tumor type. In mammary tumors, Wnt and TGFβ pathways were downregulated, whereas in renal tumors, genes related to hypoxia and DNA damage repair were downregulated.

CONCLUSIONS

Thus, our eKET diet exerts potent antitumor and antimetastatic effects in both breast and renal cancer models, albeit with different modes of action and physiologic effects. Its potential as an adjuvant dietary approach for patients with diverse cancer types should be explored further.

摘要

背景/目的:酮酯(KEs)有望成为抗癌药物,但它们对自发转移的影响仍知之甚少。尽管食用低碳水化合物、高脂肪的生酮饮食(KD)可在体内产生KEs,但KD的严格成分可能会降低癌症患者的依从性。

方法

我们研究了补充外源性酮酯(eKET)且富含碳水化合物的饮食对转移性乳腺癌(4T1-Luc)和肾癌(Renca-Luc)原位模型中肿瘤生长、转移及潜在机制的影响。在肿瘤接种后将小鼠随机分组饮食。

结果

给予KEs在体外并未改变肿瘤细胞的生长。然而,在小鼠中,我们的eKET饮食增加了循环β-羟基丁酸水平,并在两种模型中均抑制了原发性肿瘤生长和肺转移。身体成分分析表明使用eKET饮食总体安全,尽管它与肾肿瘤小鼠的脂肪量减少有关。免疫遗传学分析揭示了不同肿瘤类型肿瘤内与eKET相关的变化存在差异。在乳腺肿瘤中,Wnt和TGFβ信号通路下调,而在肾肿瘤中,与缺氧和DNA损伤修复相关的基因下调。

结论

因此,我们的eKET饮食在乳腺癌和肾癌模型中均发挥了强大的抗肿瘤和抗转移作用,尽管作用方式和生理效应有所不同。应进一步探索其作为不同癌症类型患者辅助饮食方法的潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d955/11476193/7b9fa8ba0a18/cancers-16-03390-g001.jpg

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