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Diet suppresses glioblastoma initiation in mice by maintaining quiescence of mutation-bearing neural stem cells

Glioblastoma is thought to originate from neural stem cells (NSCs) of the subventricular zone that acquire genetic alterations. In the adult brain, NSCs are largely quiescent, suggesting that deregulation of quiescence maintenance may be a prerequisite for tumor initiation. Although inactivation of...

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Autores principales: Amodeo, Valeria, Davies, Timothy, Martinez-Segura, Amalia, Clements, Melanie P., Ragdale, Holly Simpson, Bailey, Andrew, Dos Santos, Mariana Silva, MacRae, James I., Mokochinski, Joao, Kramer, Holger, Garcia-Diaz, Claudia, Gould, Alex P., Marguerat, Samuel, Parrinello, Simona
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cell Press 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10618406/
https://www.ncbi.nlm.nih.gov/pubmed/37084728
http://dx.doi.org/10.1016/j.devcel.2023.03.021
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author Amodeo, Valeria
Davies, Timothy
Martinez-Segura, Amalia
Clements, Melanie P.
Ragdale, Holly Simpson
Bailey, Andrew
Dos Santos, Mariana Silva
MacRae, James I.
Mokochinski, Joao
Kramer, Holger
Garcia-Diaz, Claudia
Gould, Alex P.
Marguerat, Samuel
Parrinello, Simona
author_facet Amodeo, Valeria
Davies, Timothy
Martinez-Segura, Amalia
Clements, Melanie P.
Ragdale, Holly Simpson
Bailey, Andrew
Dos Santos, Mariana Silva
MacRae, James I.
Mokochinski, Joao
Kramer, Holger
Garcia-Diaz, Claudia
Gould, Alex P.
Marguerat, Samuel
Parrinello, Simona
author_sort Amodeo, Valeria
collection PubMed
description Glioblastoma is thought to originate from neural stem cells (NSCs) of the subventricular zone that acquire genetic alterations. In the adult brain, NSCs are largely quiescent, suggesting that deregulation of quiescence maintenance may be a prerequisite for tumor initiation. Although inactivation of the tumor suppressor p53 is a frequent event in gliomagenesis, whether or how it affects quiescent NSCs (qNSCs) remains unclear. Here, we show that p53 maintains quiescence by inducing fatty-acid oxidation (FAO) and that acute p53 deletion in qNSCs results in their premature activation to a proliferative state. Mechanistically, this occurs through direct transcriptional induction of PPARGC1a, which in turn activates PPARα to upregulate FAO genes. Dietary supplementation with fish oil containing omega-3 fatty acids, natural PPARα ligands, fully restores quiescence of p53-deficient NSCs and delays tumor initiation in a glioblastoma mouse model. Thus, diet can silence glioblastoma driver mutations, with important implications for cancer prevention.
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spelling pubmed-106184062023-11-02 Diet suppresses glioblastoma initiation in mice by maintaining quiescence of mutation-bearing neural stem cells Amodeo, Valeria Davies, Timothy Martinez-Segura, Amalia Clements, Melanie P. Ragdale, Holly Simpson Bailey, Andrew Dos Santos, Mariana Silva MacRae, James I. Mokochinski, Joao Kramer, Holger Garcia-Diaz, Claudia Gould, Alex P. Marguerat, Samuel Parrinello, Simona Dev Cell Short Article Glioblastoma is thought to originate from neural stem cells (NSCs) of the subventricular zone that acquire genetic alterations. In the adult brain, NSCs are largely quiescent, suggesting that deregulation of quiescence maintenance may be a prerequisite for tumor initiation. Although inactivation of the tumor suppressor p53 is a frequent event in gliomagenesis, whether or how it affects quiescent NSCs (qNSCs) remains unclear. Here, we show that p53 maintains quiescence by inducing fatty-acid oxidation (FAO) and that acute p53 deletion in qNSCs results in their premature activation to a proliferative state. Mechanistically, this occurs through direct transcriptional induction of PPARGC1a, which in turn activates PPARα to upregulate FAO genes. Dietary supplementation with fish oil containing omega-3 fatty acids, natural PPARα ligands, fully restores quiescence of p53-deficient NSCs and delays tumor initiation in a glioblastoma mouse model. Thus, diet can silence glioblastoma driver mutations, with important implications for cancer prevention. Cell Press 2023-05-22 /pmc/articles/PMC10618406/ /pubmed/37084728 http://dx.doi.org/10.1016/j.devcel.2023.03.021 Text en © 2023 The Author(s) https://creativecommons.org/licenses/by/4.0/This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Short Article
Amodeo, Valeria
Davies, Timothy
Martinez-Segura, Amalia
Clements, Melanie P.
Ragdale, Holly Simpson
Bailey, Andrew
Dos Santos, Mariana Silva
MacRae, James I.
Mokochinski, Joao
Kramer, Holger
Garcia-Diaz, Claudia
Gould, Alex P.
Marguerat, Samuel
Parrinello, Simona
Diet suppresses glioblastoma initiation in mice by maintaining quiescence of mutation-bearing neural stem cells
title Diet suppresses glioblastoma initiation in mice by maintaining quiescence of mutation-bearing neural stem cells
title_full Diet suppresses glioblastoma initiation in mice by maintaining quiescence of mutation-bearing neural stem cells
title_fullStr Diet suppresses glioblastoma initiation in mice by maintaining quiescence of mutation-bearing neural stem cells
title_full_unstemmed Diet suppresses glioblastoma initiation in mice by maintaining quiescence of mutation-bearing neural stem cells
title_short Diet suppresses glioblastoma initiation in mice by maintaining quiescence of mutation-bearing neural stem cells
title_sort diet suppresses glioblastoma initiation in mice by maintaining quiescence of mutation-bearing neural stem cells
topic Short Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10618406/
https://www.ncbi.nlm.nih.gov/pubmed/37084728
http://dx.doi.org/10.1016/j.devcel.2023.03.021
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