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Cancer as a metabolic disease: implications for novel therapeutics

Carcinogenesis · 2013 · Vol. 35(3) · pp. 515–527
Thomas N. SeyfriedRoberto E. FloresAngela M. PoffDominic P. D’Agostino

Abstract

Emerging evidence indicates that cancer is primarily a metabolic disease involving disturbances in energy production through respiration and fermentation. The genomic instability observed in tumor cells and all other recognized hallmarks of cancer are considered downstream epiphenomena of the initial disturbance of cellular energy metabolism. The disturbances in tumor cell energy metabolism can be linked to abnormalities in the structure and function of the mitochondria. When viewed as a mitochondrial metabolic disease, the evolutionary theory of Lamarck can better explain cancer progression than can the evolutionary theory of Darwin. Cancer growth and progression can be managed following a whole body transition from fermentable metabolites, primarily glucose and glutamine, to respiratory metabolites, primarily ketone bodies. As each individual is a unique metabolic entity, personalization of metabolic therapy as a broad-based cancer treatment strategy will require fine-tuning to match the therapy to an individual's unique physiology.

Diet and metabolism studiesCancer, Hypoxia, and MetabolismMetabolism, Diabetes, and CancerCancerBiologyDiseaseCancer cellGenome instabilityBioinformaticsGlutamineMitochondrionPhysiologyInternal medicine

MeSH terms

Energy MetabolismHumansMitochondriaMutationNeoplasmsGenes, rasGenes, p53

Funding

  • Boston College
  • National Institutes of Health
  • Office of Naval Research
Citations
465
FWCI
14.27
field-weighted impact
References
245
Percentile
99%
vs. same field & year
Citations per year
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