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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...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cell Press
2023
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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. |
format | Online Article Text |
id | pubmed-10618406 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Cell Press |
record_format | MEDLINE/PubMed |
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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