Literature DB >> 20009300

Targeting energy metabolism in brain cancer through calorie restriction and the ketogenic diet.

B Thomas N Seyfried1, Michael Kiebish, Jeremy Marsh, Purna Mukherjee.   

Abstract

Malignant brain tumors are a significant health problem in children and adults and are largely unmanageable. As a metabolic disorder involving the dysregulation of glycolysis and respiration (the Warburg effect), malignant brain cancer can be managed through changes in metabolic environment. In contrast to malignant brain tumors that are mostly dependent on glycolysis for energy, normal neurons and glia readily transition to ketone bodies (beta-hydroxybutyrate) for energy in vivo when glucose levels are reduced. The transition from glucose to ketone bodies as a major energy source is an evolutionary conserved adaptation to food deprivation that permits the survival of normal cells during extreme shifts in nutritional environment. Only those cells with a flexible genome, honed through millions of years of environmental forcing and variability selection, can transition from one energy state to another. We propose a different approach to brain cancer management that exploits the metabolic flexibility of normal cells at the expense of the genetically defective and less metabolically flexible tumor cells. This approach to brain cancer management is supported from recent studies in orthotopic mouse brain tumor models and in human pediatric astrocytoma treated with calorie restriction and the ketogenic diet. Issues of implementation and use protocols are discussed.

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Year:  2009        PMID: 20009300     DOI: 10.4103/0973-1482.55134

Source DB:  PubMed          Journal:  J Cancer Res Ther        ISSN: 1998-4138            Impact factor:   1.805


  17 in total

1.  Untuning the tumor metabolic machine: Targeting cancer metabolism: a bedside lesson.

Authors:  Kıvanç Birsoy; David M Sabatini; Richard Possemato
Journal:  Nat Med       Date:  2012-07-06       Impact factor: 53.440

Review 2.  LDH-C4: a target with therapeutic potential for cancer and contraception.

Authors:  G S Gupta
Journal:  Mol Cell Biochem       Date:  2012-08-15       Impact factor: 3.396

Review 3.  Hypothalamic hormones and metabolism.

Authors:  Liu Lin Thio
Journal:  Epilepsy Res       Date:  2012-07       Impact factor: 3.045

Review 4.  Peroxisome proliferator activated receptor α ligands as anticancer drugs targeting mitochondrial metabolism.

Authors:  Maja Grabacka; Malgorzata Pierzchalska; Krzysztof Reiss
Journal:  Curr Pharm Biotechnol       Date:  2013       Impact factor: 2.837

5.  How does the ketogenic diet work? Four potential mechanisms.

Authors:  Nika N Danial; Adam L Hartman; Carl E Stafstrom; Liu Lin Thio
Journal:  J Child Neurol       Date:  2013-05-13       Impact factor: 1.987

6.  Increased LDH5 expression is associated with lymph node metastasis and outcome in oral squamous cell carcinoma.

Authors:  Martin Grimm; Dorothea Alexander; Adelheid Munz; Juergen Hoffmann; Siegmar Reinert
Journal:  Clin Exp Metastasis       Date:  2012-11-25       Impact factor: 5.150

7.  The ketogenic diet 2011: how it works.

Authors:  Keren Politi; Lilach Shemer-Meiri; Avinoam Shuper; S Aharoni
Journal:  Epilepsy Res Treat       Date:  2011-06-05

Review 8.  Metabolism and brain cancer.

Authors:  Suely Kazue Nagahashi Marie; Sueli Mieko Oba Shinjo
Journal:  Clinics (Sao Paulo)       Date:  2011       Impact factor: 2.365

9.  Higher carbohydrate intake is associated with increased risk of all-cause and disease-specific mortality in head and neck cancer patients: results from a prospective cohort study.

Authors:  Anna E Arthur; Amy M Goss; Wendy Demark-Wahnefried; Alison M Mondul; Kevin R Fontaine; Yi Tang Chen; William R Carroll; Sharon A Spencer; Laura Q Rogers; Laura S Rozek; Gregory T Wolf; Barbara A Gower
Journal:  Int J Cancer       Date:  2018-04-17       Impact factor: 7.396

10.  Epilepsy's Big Fat Answer.

Authors:  John M Freeman
Journal:  Cerebrum       Date:  2013-03-01
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