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      Short-term fasting in glioma patients: analysis of diet diaries and metabolic parameters of the ERGO2 trial

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          Abstract

          Purpose

          The prospective, randomized ERGO2 trial investigated the effect of calorie-restricted ketogenic diet and intermittent fasting (KD-IF) on re-irradiation for recurrent brain tumors. The study did not meet its primary endpoint of improved progression-free survival in comparison to standard diet (SD). We here report the results of the quality of life/neurocognition and a detailed analysis of the diet diaries.

          Methods

          50 patients were randomized 1:1 to re-irradiation combined with either SD or KD-IF. The KD-IF schedule included 3 days of ketogenic diet (KD: 21–23 kcal/kg/d, carbohydrate intake limited to 50 g/d), followed by 3 days of fasting and again 3 days of KD. Follow-up included examination of cognition, quality of life and serum samples.

          Results

          The 20 patients who completed KD-IF met the prespecified goals for calorie and carbohydrate restriction. Substantial decreases in leptin and insulin and an increase in uric acid were observed. The SD group, of note, had a lower calorie intake than expected (21 kcal/kg/d instead of 30 kcal/kg/d). Neither quality of life nor cognition were affected by the diet. Low glucose emerged as a significant prognostic parameter in a best responder analysis.

          Conclusion

          The strict caloric goals of the ERGO2 trial were tolerated well by patients with recurrent brain cancer. The short diet schedule led to significant metabolic changes with low glucose emerging as a candidate marker of better prognosis. The unexpected lower calorie intake of the control group complicates the interpretation of the results.

          Clinicaltrials.gov number: NCT01754350; Registration: 21.12.2012.

          Supplementary Information

          The online version contains supplementary material available at 10.1007/s00394-021-02666-1.

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          Most cited references43

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          Hallmarks of Cancer: The Next Generation

          The hallmarks of cancer comprise six biological capabilities acquired during the multistep development of human tumors. The hallmarks constitute an organizing principle for rationalizing the complexities of neoplastic disease. They include sustaining proliferative signaling, evading growth suppressors, resisting cell death, enabling replicative immortality, inducing angiogenesis, and activating invasion and metastasis. Underlying these hallmarks are genome instability, which generates the genetic diversity that expedites their acquisition, and inflammation, which fosters multiple hallmark functions. Conceptual progress in the last decade has added two emerging hallmarks of potential generality to this list-reprogramming of energy metabolism and evading immune destruction. In addition to cancer cells, tumors exhibit another dimension of complexity: they contain a repertoire of recruited, ostensibly normal cells that contribute to the acquisition of hallmark traits by creating the "tumor microenvironment." Recognition of the widespread applicability of these concepts will increasingly affect the development of new means to treat human cancer. Copyright © 2011 Elsevier Inc. All rights reserved.
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            Suppression of oxidative stress by β-hydroxybutyrate, an endogenous histone deacetylase inhibitor.

            Concentrations of acetyl-coenzyme A and nicotinamide adenine dinucleotide (NAD(+)) affect histone acetylation and thereby couple cellular metabolic status and transcriptional regulation. We report that the ketone body d-β-hydroxybutyrate (βOHB) is an endogenous and specific inhibitor of class I histone deacetylases (HDACs). Administration of exogenous βOHB, or fasting or calorie restriction, two conditions associated with increased βOHB abundance, all increased global histone acetylation in mouse tissues. Inhibition of HDAC by βOHB was correlated with global changes in transcription, including that of the genes encoding oxidative stress resistance factors FOXO3A and MT2. Treatment of cells with βOHB increased histone acetylation at the Foxo3a and Mt2 promoters, and both genes were activated by selective depletion of HDAC1 and HDAC2. Consistent with increased FOXO3A and MT2 activity, treatment of mice with βOHB conferred substantial protection against oxidative stress.
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              Suppression of insulin feedback enhances the efficacy of PI3K inhibitors

              Mutations in PIK3CA, encoding the insulin-activated phosphoinositide-3-kinase (PI3K), and loss of function mutations in PTEN, a phosphatase that degrades the phosphoinositide lipids generated by PI3K, are among the most frequent events in human cancers 1,2 . Yet, pharmacological inhibition of PI3K has resulted in variable clinical responses, raising the possibility of an inherent mechanism of resistance. Since the PIK3CA-encoded enzyme, p110α, mediates virtually all cellular responses to insulin, targeted inhibition of this enzyme disrupts glucose metabolism in multiple tissue types. For example, blocking insulin signaling promotes glycogen breakdown in the liver and prevents glucose uptake in the skeletal muscle and adipose tissue, resulting in transient hyperglycemia that occurs within a few hours of PI3K inhibition. The effect is usually transient because compensatory insulin release from the pancreas (i.e. insulin feedback) restores normal glucose homeostasis3. However, the hyperglycemia may be exacerbated or prolonged in patients with any degree of insulin resistance and, in these cases, requires discontinuation of therapy 3–6 . We hypothesized that insulin feedback induced by PI3K inhibitors may be reactivating the PI3K-mTOR signaling axis in tumors, compromising their effectiveness 7,8 . Here, we show in several model tumors, that systemic glucose-insulin feedback caused by targeted inhibition of this pathway is sufficient to activate PI3K signaling, even in the presence of PI3K inhibitors. We demonstrate that this insulin feedback can be prevented using dietary or pharmaceutical approaches, which greatly enhance the efficacy/toxicity ratios of these compounds. These findings have direct clinical implications for the multiple p110α inhibitors that are in clinical trials and provide a means to significantly increase treatment efficacy for patients with a myriad of tumor types.
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                Author and article information

                Contributors
                martin.voss@kgu.de
                Journal
                Eur J Nutr
                Eur J Nutr
                European Journal of Nutrition
                Springer Berlin Heidelberg (Berlin/Heidelberg )
                1436-6207
                1436-6215
                6 September 2021
                6 September 2021
                2022
                : 61
                : 1
                : 477-487
                Affiliations
                [1 ]GRID grid.411088.4, ISNI 0000 0004 0578 8220, Dr. Senckenberg Institute of Neurooncology, , University Hospital Frankfurt, Goethe University, ; Schleusenweg 2-16, 60528 Frankfurt/Main, Germany
                [2 ]GRID grid.411088.4, ISNI 0000 0004 0578 8220, University Cancer Center Frankfurt (UCT), , University Hospital Frankfurt, Goethe University, ; Theodor-Stern-Kai 7, 60590 Frankfurt/Main, Germany
                [3 ]GRID grid.7497.d, ISNI 0000 0004 0492 0584, Partner Site Frankfurt/Mainz, German Cancer Research Center (DKFZ), , German Cancer Consortium (DKTK), Stiftung Des Öffentlichen Rechts, ; Im Neuenheimer Feld 280, 69120 Heidelberg, Germany
                [4 ]GRID grid.511198.5, Frankfurt Cancer Institute (FCI), ; Georg-Speyer-Haus, Paul-Ehrlich-Straße 42-44, 60596 Frankfurt/Main, Germany
                [5 ]GRID grid.411088.4, ISNI 0000 0004 0578 8220, Institute of Neuroradiology, , University Hospital Frankfurt, Goethe University, ; Schleusenweg 2-16, 60528 Frankfurt/Main, Germany
                [6 ]GRID grid.411088.4, ISNI 0000 0004 0578 8220, Department of Medicine 1, , University Hospital Frankfurt, Goethe University, ; Theodor-Stern-Kai 7, 60590 Frankfurt/Main, Germany
                [7 ]GRID grid.411088.4, ISNI 0000 0004 0578 8220, Department of Neurosurgery, , University Hospital Frankfurt, Goethe University, ; Schleusenweg 2-16, 60528 Frankfurt/Main, Germany
                [8 ]Department of Neurosurgery, HELIOS Hospital Erfurt, Nordhäuser Straße 74, 99089 Erfurt, Germany
                [9 ]GRID grid.411088.4, ISNI 0000 0004 0578 8220, Institute of Neurology (Edinger-Institute), , University Hospital Frankfurt, Goethe University, ; Heinrich-Hoffmann Strasse 7, 60528 Frankfurt/Main, Germany
                [10 ]GRID grid.411088.4, ISNI 0000 0004 0578 8220, Department of Radiotherapy and Oncology, , University Hospital Frankfurt, Goethe University, ; Theodor-Stern-Kai 7, 60590 Frankfurt/Main, Germany
                [11 ]GRID grid.411544.1, ISNI 0000 0001 0196 8249, Interdisciplinary Division of Neuro-Oncology, , University Hospital Tübingen, ; Hoppe-Seyler-Straße 3, 72076 Tübingen, Germany
                Author information
                http://orcid.org/0000-0001-8469-8204
                http://orcid.org/0000-0002-8640-6858
                http://orcid.org/0000-0002-1402-6290
                http://orcid.org/0000-0001-5530-6910
                Article
                2666
                10.1007/s00394-021-02666-1
                8783850
                34487222
                58fac5f1-b170-4917-a4c3-e3ba51ace4a9
                © The Author(s) 2021

                Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.

                History
                : 7 June 2021
                : 19 August 2021
                Funding
                Funded by: Universitätsklinikum Frankfurt (8916)
                Funded by: Johann Wolfgang Goethe-Universität, Frankfurt am Main (1022)
                Categories
                Original Contribution
                Custom metadata
                © The Author(s), under exclusive licence to Springer-Verlag GmbH Germany 2022

                Nutrition & Dietetics
                glioblastoma,radiation,ketogenic diet,fasting,glucose,leptin
                Nutrition & Dietetics
                glioblastoma, radiation, ketogenic diet, fasting, glucose, leptin

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