AMPK Is a Negative Regulator of the Warburg Effect and Suppresses Tumor Growth In Vivo

被引:769
作者
Faubert, Brandon [1 ,4 ]
Boily, Gino [1 ,4 ]
Izreig, Said [1 ,4 ]
Griss, Takla [1 ,4 ]
Samborska, Bozena [1 ,4 ]
Dong, Zhifeng [4 ]
Dupuy, Fanny [2 ,4 ]
Chambers, Christopher [6 ]
Fuerth, Benjamin J. [1 ,4 ]
Viollet, Benoit [8 ,9 ,10 ]
Mamer, Orval A. [4 ,5 ]
Avizonis, Daina [4 ,5 ]
DeBerardinis, Ralph J. [6 ,7 ,11 ]
Siegel, Peter M. [2 ,3 ,4 ]
Jones, Russell G. [1 ,4 ]
机构
[1] McGill Univ, Dept Physiol, Montreal, PQ H3G 1Y6, Canada
[2] McGill Univ, Dept Biochem, Montreal, PQ H3G 1Y6, Canada
[3] McGill Univ, Dept Med, Montreal, PQ H3G 1Y6, Canada
[4] McGill Univ, Goodman Canc Res Ctr, Montreal, PQ H3A 1A3, Canada
[5] McGill Univ, Metabol Core Facil, Montreal, PQ H3A 1A3, Canada
[6] Univ Texas SW Med Ctr Dallas, Childrens Med Ctr, Res Inst, Dallas, TX 75390 USA
[7] Univ Texas SW Med Ctr Dallas, McDermott Ctr Human Growth & Dev, Dallas, TX 75390 USA
[8] Inst Cochin Genet Mol, INSERM, U1016, F-75014 Paris, France
[9] CNRS, UMR 8104, F-75014 Paris, France
[10] Univ Paris 05, F-75014 Paris, France
[11] Univ Texas SW Med Ctr Dallas, Harold C Simmons Comprehens Canc Ctr, Dallas, TX 75235 USA
基金
美国国家卫生研究院; 加拿大健康研究院;
关键词
ACTIVATED PROTEIN-KINASE; METABOLIC STRESS; ENERGY SENSOR; CELL-GROWTH; CANCER; MTOR; PHOSPHORYLATION; LKB1; METFORMIN; TRANSCRIPTION;
D O I
10.1016/j.cmet.2012.12.001
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
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 alpha 1 catalytic subunit of AMPK accelerates Myc-induced lymphomagenesis. Inactivation of AMPK alpha 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-1 alpha (HIF-1 alpha), as silencing HIF-1 alpha reverses the shift to aerobic glycolysis and the biosynthetic and proliferative advantages conferred by reduced AMPK alpha 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.
引用
收藏
页码:113 / 124
页数:12
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