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Hyperpolarized (13)C-glucose magnetic resonance highlights reduced aerobic glycolysis in vivo in infiltrative glioblastoma

Glioblastoma (GBM) is the most aggressive brain tumor type in adults. GBM is heterogeneous, with a compact core lesion surrounded by an invasive tumor front. This front is highly relevant for tumor recurrence but is generally non-detectable using standard imaging techniques. Recent studies demonstra...

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Autores principales: Mishkovsky, Mor, Gusyatiner, Olga, Lanz, Bernard, Cudalbu, Cristina, Vassallo, Irene, Hamou, Marie-France, Bloch, Jocelyne, Comment, Arnaud, Gruetter, Rolf, Hegi, Monika E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7952603/
https://www.ncbi.nlm.nih.gov/pubmed/33707647
http://dx.doi.org/10.1038/s41598-021-85339-7
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author Mishkovsky, Mor
Gusyatiner, Olga
Lanz, Bernard
Cudalbu, Cristina
Vassallo, Irene
Hamou, Marie-France
Bloch, Jocelyne
Comment, Arnaud
Gruetter, Rolf
Hegi, Monika E.
author_facet Mishkovsky, Mor
Gusyatiner, Olga
Lanz, Bernard
Cudalbu, Cristina
Vassallo, Irene
Hamou, Marie-France
Bloch, Jocelyne
Comment, Arnaud
Gruetter, Rolf
Hegi, Monika E.
author_sort Mishkovsky, Mor
collection PubMed
description Glioblastoma (GBM) is the most aggressive brain tumor type in adults. GBM is heterogeneous, with a compact core lesion surrounded by an invasive tumor front. This front is highly relevant for tumor recurrence but is generally non-detectable using standard imaging techniques. Recent studies demonstrated distinct metabolic profiles of the invasive phenotype in GBM. Magnetic resonance (MR) of hyperpolarized (13)C-labeled probes is a rapidly advancing field that provides real-time metabolic information. Here, we applied hyperpolarized (13)C-glucose MR to mouse GBM models. Compared to controls, the amount of lactate produced from hyperpolarized glucose was higher in the compact GBM model, consistent with the accepted “Warburg effect”. However, the opposite response was observed in models reflecting the invasive zone, with less lactate produced than in controls, implying a reduction in aerobic glycolysis. These striking differences could be used to map the metabolic heterogeneity in GBM and to visualize the infiltrative front of GBM.
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spelling pubmed-79526032021-03-15 Hyperpolarized (13)C-glucose magnetic resonance highlights reduced aerobic glycolysis in vivo in infiltrative glioblastoma Mishkovsky, Mor Gusyatiner, Olga Lanz, Bernard Cudalbu, Cristina Vassallo, Irene Hamou, Marie-France Bloch, Jocelyne Comment, Arnaud Gruetter, Rolf Hegi, Monika E. Sci Rep Article Glioblastoma (GBM) is the most aggressive brain tumor type in adults. GBM is heterogeneous, with a compact core lesion surrounded by an invasive tumor front. This front is highly relevant for tumor recurrence but is generally non-detectable using standard imaging techniques. Recent studies demonstrated distinct metabolic profiles of the invasive phenotype in GBM. Magnetic resonance (MR) of hyperpolarized (13)C-labeled probes is a rapidly advancing field that provides real-time metabolic information. Here, we applied hyperpolarized (13)C-glucose MR to mouse GBM models. Compared to controls, the amount of lactate produced from hyperpolarized glucose was higher in the compact GBM model, consistent with the accepted “Warburg effect”. However, the opposite response was observed in models reflecting the invasive zone, with less lactate produced than in controls, implying a reduction in aerobic glycolysis. These striking differences could be used to map the metabolic heterogeneity in GBM and to visualize the infiltrative front of GBM. Nature Publishing Group UK 2021-03-11 /pmc/articles/PMC7952603/ /pubmed/33707647 http://dx.doi.org/10.1038/s41598-021-85339-7 Text en © The Author(s) 2021 Open Access This 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/.
spellingShingle Article
Mishkovsky, Mor
Gusyatiner, Olga
Lanz, Bernard
Cudalbu, Cristina
Vassallo, Irene
Hamou, Marie-France
Bloch, Jocelyne
Comment, Arnaud
Gruetter, Rolf
Hegi, Monika E.
Hyperpolarized (13)C-glucose magnetic resonance highlights reduced aerobic glycolysis in vivo in infiltrative glioblastoma
title Hyperpolarized (13)C-glucose magnetic resonance highlights reduced aerobic glycolysis in vivo in infiltrative glioblastoma
title_full Hyperpolarized (13)C-glucose magnetic resonance highlights reduced aerobic glycolysis in vivo in infiltrative glioblastoma
title_fullStr Hyperpolarized (13)C-glucose magnetic resonance highlights reduced aerobic glycolysis in vivo in infiltrative glioblastoma
title_full_unstemmed Hyperpolarized (13)C-glucose magnetic resonance highlights reduced aerobic glycolysis in vivo in infiltrative glioblastoma
title_short Hyperpolarized (13)C-glucose magnetic resonance highlights reduced aerobic glycolysis in vivo in infiltrative glioblastoma
title_sort hyperpolarized (13)c-glucose magnetic resonance highlights reduced aerobic glycolysis in vivo in infiltrative glioblastoma
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7952603/
https://www.ncbi.nlm.nih.gov/pubmed/33707647
http://dx.doi.org/10.1038/s41598-021-85339-7
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