Department of Physiology, McGill University, Montreal, QC, H3G 1Y6, Canada.
Cell Metab. 2013 Jan 8;17(1):113-24. doi: 10.1016/j.cmet.2012.12.001. Epub 2012 Dec 27.
AMPK is a metabolic sensor that helps maintain cellular energy homeostasis. Despite evidence linking AMPK with tumor suppressor functions, the role of AMPK in tumorigenesis and tumor metabolism is unknown. Here we show that AMPK negatively regulates aerobic glycolysis (the Warburg effect) in cancer cells and suppresses tumor growth in vivo. Genetic ablation of the α1 catalytic subunit of AMPK accelerates Myc-induced lymphomagenesis. Inactivation of AMPKα in both transformed and nontransformed cells promotes a metabolic shift to aerobic glycolysis, increased allocation of glucose carbon into lipids, and biomass accumulation. These metabolic effects require normoxic stabilization of the hypoxia-inducible factor-1α (HIF-1α), as silencing HIF-1α reverses the shift to aerobic glycolysis and the biosynthetic and proliferative advantages conferred by reduced AMPKα signaling. Together our findings suggest that AMPK activity opposes tumor development and that its loss fosters tumor progression in part by regulating cellular metabolic pathways that support cell growth and proliferation.
AMPK 是一种代谢传感器,有助于维持细胞能量稳态。尽管有证据表明 AMPK 与肿瘤抑制功能有关,但 AMPK 在肿瘤发生和肿瘤代谢中的作用尚不清楚。在这里,我们表明 AMPK 负调控癌细胞中的有氧糖酵解(Warburg 效应),并在体内抑制肿瘤生长。AMPK 的 α1 催化亚基的遗传缺失加速了 Myc 诱导的淋巴瘤发生。在转化和非转化细胞中 AMPKα 的失活促进了代谢向有氧糖酵解的转变,增加了葡萄糖碳向脂质的分配,以及生物量的积累。这些代谢效应需要缺氧诱导因子-1α(HIF-1α)的正常氧稳定,因为沉默 HIF-1α 可逆转向有氧糖酵解的转变,以及由降低的 AMPKα 信号转导赋予的合成和增殖优势。总之,我们的研究结果表明,AMPK 活性与肿瘤的发生相拮抗,其缺失通过调节支持细胞生长和增殖的细胞代谢途径,在一定程度上促进了肿瘤的进展。