Bioanalytical Research Laboratories, Department of Biosciences and Cancer Cluster Salzburg, University of Salzburg, Hellbrunnerstraße 34, 5020 Salzburg, Austria.
Research Program for Receptor Biochemistry and Tumor Metabolism, Department of Pediatrics, Paracelsus Medical University, 5020 Salzburg, Austria.
Int J Mol Sci. 2019 Aug 8;20(16):3873. doi: 10.3390/ijms20163873.
The application of ketogenic diet (KD) (high fat/low carbohydrate/adequate protein) as an auxiliary cancer therapy is a field of growing attention. KD provides sufficient energy supply for healthy cells, while possibly impairing energy production in highly glycolytic tumor cells. Moreover, KD regulates insulin and tumor related growth factors (like insulin growth factor-1, IGF-1). In order to provide molecular evidence for the proposed additional inhibition of tumor growth when combining chemotherapy with KD, we applied untargeted quantitative metabolome analysis on a spontaneous breast cancer xenograft mouse model, using MDA-MB-468 cells. Healthy mice and mice bearing breast cancer xenografts and receiving cyclophosphamide chemotherapy were compared after treatment with control diet and KD. Metabolomic profiling was performed on plasma samples, applying high-performance liquid chromatography coupled to tandem mass spectrometry. Statistical analysis revealed metabolic fingerprints comprising numerous significantly regulated features in the group of mice bearing breast cancer. This fingerprint disappeared after treatment with KD, resulting in recovery to the metabolic status observed in healthy mice receiving control diet. Moreover, amino acid metabolism as well as fatty acid transport were found to be affected by both the tumor and the applied KD. Our results provide clear evidence of a significant molecular effect of adjuvant KD in the context of tumor growth inhibition and suggest additional mechanisms of tumor suppression beyond the proposed constrain in energy supply of tumor cells.
生酮饮食(KD)(高脂肪/低碳水化合物/适量蛋白质)作为辅助癌症治疗的应用是一个备受关注的领域。KD 为健康细胞提供了充足的能量供应,同时可能损害高度糖酵解的肿瘤细胞的能量产生。此外,KD 还调节胰岛素和与肿瘤相关的生长因子(如胰岛素生长因子-1,IGF-1)。为了为联合化疗和 KD 时提出的额外抑制肿瘤生长提供分子证据,我们在自发乳腺癌异种移植小鼠模型上应用了非靶向定量代谢组学分析,使用 MDA-MB-468 细胞。在接受环磷酰胺化疗后,比较了健康小鼠、荷乳腺癌异种移植小鼠和接受 KD 的小鼠。对血浆样本进行代谢组学分析,应用高效液相色谱-串联质谱联用技术。统计分析显示,在荷乳腺癌的小鼠组中存在包含许多显著调节特征的代谢指纹。在用 KD 治疗后,这种指纹消失了,导致代谢状态恢复到接受对照饮食的健康小鼠的状态。此外,发现氨基酸代谢和脂肪酸转运都受到肿瘤和应用 KD 的影响。我们的结果提供了明确的证据,表明辅助 KD 在肿瘤生长抑制方面具有显著的分子作用,并提示了除了肿瘤细胞能量供应受限之外的抑制肿瘤的其他机制。