Department of Medical Oncology, Dana-Farber Cancer Institute, Harvard Medical School, Boston, MA, USA.
Center for Functional Cancer Epigenetics, Dana-Farber Cancer Institute, Boston, MA, USA.
Nat Commun. 2019 Sep 25;10(1):4358. doi: 10.1038/s41467-019-12298-z.
Systemic metabolic alterations associated with increased consumption of saturated fat and obesity are linked with increased risk of prostate cancer progression and mortality, but the molecular underpinnings of this association are poorly understood. Here, we demonstrate in a murine prostate cancer model, that high-fat diet (HFD) enhances the MYC transcriptional program through metabolic alterations that favour histone H4K20 hypomethylation at the promoter regions of MYC regulated genes, leading to increased cellular proliferation and tumour burden. Saturated fat intake (SFI) is also associated with an enhanced MYC transcriptional signature in prostate cancer patients. The SFI-induced MYC signature independently predicts prostate cancer progression and death. Finally, switching from a high-fat to a low-fat diet, attenuates the MYC transcriptional program in mice. Our findings suggest that in primary prostate cancer, dietary SFI contributes to tumour progression by mimicking MYC over expression, setting the stage for therapeutic approaches involving changes to the diet.
与饱和脂肪摄入增加和肥胖相关的系统性代谢改变与前列腺癌进展和死亡风险增加相关,但这种关联的分子基础知之甚少。在这里,我们在小鼠前列腺癌模型中证明,高脂肪饮食(HFD)通过代谢改变增强 MYC 转录程序,有利于 MYC 调控基因启动子区域的组蛋白 H4K20 低甲基化,导致细胞增殖和肿瘤负担增加。饱和脂肪摄入(SFI)也与前列腺癌患者中增强的 MYC 转录特征相关。SFI 诱导的 MYC 特征独立预测前列腺癌的进展和死亡。最后,从高脂肪饮食切换到低脂肪饮食可减弱小鼠中的 MYC 转录程序。我们的研究结果表明,在原发性前列腺癌中,饮食 SFI 通过模拟 MYC 过表达促进肿瘤进展,为涉及饮食改变的治疗方法奠定了基础。