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Glioblastoma Utilizes Fatty Acids and Ketone Bodies for Growth Allowing Progression during Ketogenic Diet Therapy

Glioblastoma (GBM) metabolism has traditionally been characterized by a primary dependence on aerobic glycolysis, prompting the use of the ketogenic diet (KD) as a potential therapy. In this study we evaluated the effectiveness of the KD in GBM and assessed the role of fatty acid oxidation (FAO) in...

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Autores principales: Sperry, Jantzen, Condro, Michael C., Guo, Lea, Braas, Daniel, Vanderveer-Harris, Nathan, Kim, Kristen K.O., Pope, Whitney B., Divakaruni, Ajit S., Lai, Albert, Christofk, Heather, Castro, Maria G., Lowenstein, Pedro R., Le Belle, Janel E., Kornblum, Harley I.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7471621/
https://www.ncbi.nlm.nih.gov/pubmed/32861192
http://dx.doi.org/10.1016/j.isci.2020.101453
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author Sperry, Jantzen
Condro, Michael C.
Guo, Lea
Braas, Daniel
Vanderveer-Harris, Nathan
Kim, Kristen K.O.
Pope, Whitney B.
Divakaruni, Ajit S.
Lai, Albert
Christofk, Heather
Castro, Maria G.
Lowenstein, Pedro R.
Le Belle, Janel E.
Kornblum, Harley I.
author_facet Sperry, Jantzen
Condro, Michael C.
Guo, Lea
Braas, Daniel
Vanderveer-Harris, Nathan
Kim, Kristen K.O.
Pope, Whitney B.
Divakaruni, Ajit S.
Lai, Albert
Christofk, Heather
Castro, Maria G.
Lowenstein, Pedro R.
Le Belle, Janel E.
Kornblum, Harley I.
author_sort Sperry, Jantzen
collection PubMed
description Glioblastoma (GBM) metabolism has traditionally been characterized by a primary dependence on aerobic glycolysis, prompting the use of the ketogenic diet (KD) as a potential therapy. In this study we evaluated the effectiveness of the KD in GBM and assessed the role of fatty acid oxidation (FAO) in promoting GBM propagation. In vitro assays revealed FA utilization throughout the GBM metabolome and growth inhibition in nearly every cell line in a broad spectrum of patient-derived glioma cells treated with FAO inhibitors. In vivo assessments revealed that knockdown of carnitine palmitoyltransferase 1A (CPT1A), the rate-limiting enzyme for FAO, reduced the rate of tumor growth and increased survival. However, the unrestricted ketogenic diet did not reduce tumor growth and for some models significantly reduced survival. Altogether, these data highlight important roles for FA and ketone body metabolism that could serve to improve targeted therapies in GBM.
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spelling pubmed-74716212020-09-09 Glioblastoma Utilizes Fatty Acids and Ketone Bodies for Growth Allowing Progression during Ketogenic Diet Therapy Sperry, Jantzen Condro, Michael C. Guo, Lea Braas, Daniel Vanderveer-Harris, Nathan Kim, Kristen K.O. Pope, Whitney B. Divakaruni, Ajit S. Lai, Albert Christofk, Heather Castro, Maria G. Lowenstein, Pedro R. Le Belle, Janel E. Kornblum, Harley I. iScience Article Glioblastoma (GBM) metabolism has traditionally been characterized by a primary dependence on aerobic glycolysis, prompting the use of the ketogenic diet (KD) as a potential therapy. In this study we evaluated the effectiveness of the KD in GBM and assessed the role of fatty acid oxidation (FAO) in promoting GBM propagation. In vitro assays revealed FA utilization throughout the GBM metabolome and growth inhibition in nearly every cell line in a broad spectrum of patient-derived glioma cells treated with FAO inhibitors. In vivo assessments revealed that knockdown of carnitine palmitoyltransferase 1A (CPT1A), the rate-limiting enzyme for FAO, reduced the rate of tumor growth and increased survival. However, the unrestricted ketogenic diet did not reduce tumor growth and for some models significantly reduced survival. Altogether, these data highlight important roles for FA and ketone body metabolism that could serve to improve targeted therapies in GBM. Elsevier 2020-08-13 /pmc/articles/PMC7471621/ /pubmed/32861192 http://dx.doi.org/10.1016/j.isci.2020.101453 Text en © 2020 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Article
Sperry, Jantzen
Condro, Michael C.
Guo, Lea
Braas, Daniel
Vanderveer-Harris, Nathan
Kim, Kristen K.O.
Pope, Whitney B.
Divakaruni, Ajit S.
Lai, Albert
Christofk, Heather
Castro, Maria G.
Lowenstein, Pedro R.
Le Belle, Janel E.
Kornblum, Harley I.
Glioblastoma Utilizes Fatty Acids and Ketone Bodies for Growth Allowing Progression during Ketogenic Diet Therapy
title Glioblastoma Utilizes Fatty Acids and Ketone Bodies for Growth Allowing Progression during Ketogenic Diet Therapy
title_full Glioblastoma Utilizes Fatty Acids and Ketone Bodies for Growth Allowing Progression during Ketogenic Diet Therapy
title_fullStr Glioblastoma Utilizes Fatty Acids and Ketone Bodies for Growth Allowing Progression during Ketogenic Diet Therapy
title_full_unstemmed Glioblastoma Utilizes Fatty Acids and Ketone Bodies for Growth Allowing Progression during Ketogenic Diet Therapy
title_short Glioblastoma Utilizes Fatty Acids and Ketone Bodies for Growth Allowing Progression during Ketogenic Diet Therapy
title_sort glioblastoma utilizes fatty acids and ketone bodies for growth allowing progression during ketogenic diet therapy
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7471621/
https://www.ncbi.nlm.nih.gov/pubmed/32861192
http://dx.doi.org/10.1016/j.isci.2020.101453
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