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生酮饮食增强肺癌异种移植的氧化应激和放化疗反应。

Ketogenic diets enhance oxidative stress and radio-chemo-therapy responses in lung cancer xenografts.

机构信息

Free Radical and Radiation Biology Program, Department of Radiation Oncology, Holden Comprehensive Cancer Center, The University of Iowa, Iowa City, Iowa 52242, USA.

出版信息

Clin Cancer Res. 2013 Jul 15;19(14):3905-13. doi: 10.1158/1078-0432.CCR-12-0287. Epub 2013 Jun 6.

Abstract

PURPOSE

Ketogenic diets are high in fat and low in carbohydrates as well as protein which forces cells to rely on lipid oxidation and mitochondrial respiration rather than glycolysis for energy metabolism. Cancer cells (relative to normal cells) are believed to exist in a state of chronic oxidative stress mediated by mitochondrial metabolism. The current study tests the hypothesis that ketogenic diets enhance radio-chemo-therapy responses in lung cancer xenografts by enhancing oxidative stress.

EXPERIMENTAL DESIGN

Mice bearing NCI-H292 and A549 lung cancer xenografts were fed a ketogenic diet (KetoCal 4:1 fats: proteins+carbohydrates) and treated with either conventionally fractionated (1.8-2 Gy) or hypofractionated (6 Gy) radiation as well as conventionally fractionated radiation combined with carboplatin. Mice weights and tumor size were monitored. Tumors were assessed for immunoreactive 4-hydroxy-2-nonenal-(4HNE)-modified proteins as a marker of oxidative stress as well as proliferating cell nuclear antigen (PCNA) and γH2AX as indices of proliferation and DNA damage, respectively.

RESULTS

The ketogenic diets combined with radiation resulted in slower tumor growth in both NCI-H292 and A549 xenografts (P < 0.05), relative to radiation alone. The ketogenic diet also slowed tumor growth when combined with carboplatin and radiation, relative to control. Tumors from animals fed a ketogenic diet in combination with radiation showed increases in oxidative damage mediated by lipid peroxidation as determined by 4HNE-modified proteins as well as decreased proliferation as assessed by decreased immunoreactive PCNA.

CONCLUSIONS

These results show that a ketogenic diet enhances radio-chemo-therapy responses in lung cancer xenografts by a mechanism that may involve increased oxidative stress.

摘要

目的

生酮饮食富含脂肪,碳水化合物和蛋白质含量低,这迫使细胞依赖脂质氧化和线粒体呼吸来进行能量代谢,而不是糖酵解。与正常细胞相比,癌细胞(relative to normal cells) 被认为处于由线粒体代谢介导的慢性氧化应激状态。本研究通过检测氧化应激来检验生酮饮食增强肺癌异种移植体放射化疗反应的假设。

实验设计

携带 NCI-H292 和 A549 肺癌异种移植瘤的小鼠喂食生酮饮食(KetoCal 4:1 脂肪:蛋白质+碳水化合物),并接受常规分割(1.8-2 Gy)或低分割(6 Gy)放疗以及常规分割放疗联合卡铂治疗。监测小鼠体重和肿瘤大小。评估肿瘤中作为氧化应激标志物的 4-羟基-2-壬烯醛(4HNE)修饰蛋白以及增殖细胞核抗原(PCNA)和 γH2AX 的免疫反应性,分别作为增殖和 DNA 损伤的指标。

结果

与单独放疗相比,生酮饮食联合放疗可使 NCI-H292 和 A549 异种移植瘤的肿瘤生长速度减慢(P < 0.05)。生酮饮食联合卡铂和放疗也使肿瘤生长速度减慢,与对照组相比。与单独放疗相比,接受生酮饮食联合放疗的动物的肿瘤显示脂质过氧化介导的氧化损伤增加,如 4HNE 修饰蛋白所示,增殖减少,如免疫反应性 PCNA 减少所示。

结论

这些结果表明,生酮饮食通过增加氧化应激的机制增强肺癌异种移植体的放射化疗反应。

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