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Activation of the mevalonate pathway in response to anti-cancer treatments drives glioblastoma recurrences through activation of Rac-1
Glioblastoma is the deadliest adult brain cancer. Under the current standard of care almost all patients succumb to the disease and novel treatments are urgently needed. Dopamine receptor antagonists have been shown to target cancer cell plasticity in GBM and repurposing these FDA-approved drugs in...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cold Spring Harbor Laboratory
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10402033/ https://www.ncbi.nlm.nih.gov/pubmed/37546917 http://dx.doi.org/10.1101/2023.07.23.550205 |
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author | He, Ling Ioannidis, Angeliki Arambula, Evelyn Hoffman, Carter J. Joshi, Purva Kathiravan, Anoushka Whitelegge, Julian Liau, Linda M. Kornblum, Harley I. Pajonk, Frank |
author_facet | He, Ling Ioannidis, Angeliki Arambula, Evelyn Hoffman, Carter J. Joshi, Purva Kathiravan, Anoushka Whitelegge, Julian Liau, Linda M. Kornblum, Harley I. Pajonk, Frank |
author_sort | He, Ling |
collection | PubMed |
description | Glioblastoma is the deadliest adult brain cancer. Under the current standard of care almost all patients succumb to the disease and novel treatments are urgently needed. Dopamine receptor antagonists have been shown to target cancer cell plasticity in GBM and repurposing these FDA-approved drugs in combination with radiation improves the efficacy of radiotherapy in glioma models. In cells surviving this combination treatment the mevalonate pathway is upregulated at the transcriptional and functional level. Here we report that glioblastoma treatments that converge in the immediate early response to radiation through activation of the MAPK cascade universally upregulate the mevalonate pathway and increase stemness of GBM cells through activation of the Rho-GTPase Rac-1. Activation of the mevalonate pathway and Rac-1 is inhibited by statins, which leads to improved survival in mouse models of glioblastoma when combined with radiation and drugs that target the glioma stem cell pool and plasticity of glioma cells. |
format | Online Article Text |
id | pubmed-10402033 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Cold Spring Harbor Laboratory |
record_format | MEDLINE/PubMed |
spelling | pubmed-104020332023-08-05 Activation of the mevalonate pathway in response to anti-cancer treatments drives glioblastoma recurrences through activation of Rac-1 He, Ling Ioannidis, Angeliki Arambula, Evelyn Hoffman, Carter J. Joshi, Purva Kathiravan, Anoushka Whitelegge, Julian Liau, Linda M. Kornblum, Harley I. Pajonk, Frank bioRxiv Article Glioblastoma is the deadliest adult brain cancer. Under the current standard of care almost all patients succumb to the disease and novel treatments are urgently needed. Dopamine receptor antagonists have been shown to target cancer cell plasticity in GBM and repurposing these FDA-approved drugs in combination with radiation improves the efficacy of radiotherapy in glioma models. In cells surviving this combination treatment the mevalonate pathway is upregulated at the transcriptional and functional level. Here we report that glioblastoma treatments that converge in the immediate early response to radiation through activation of the MAPK cascade universally upregulate the mevalonate pathway and increase stemness of GBM cells through activation of the Rho-GTPase Rac-1. Activation of the mevalonate pathway and Rac-1 is inhibited by statins, which leads to improved survival in mouse models of glioblastoma when combined with radiation and drugs that target the glioma stem cell pool and plasticity of glioma cells. Cold Spring Harbor Laboratory 2023-07-25 /pmc/articles/PMC10402033/ /pubmed/37546917 http://dx.doi.org/10.1101/2023.07.23.550205 Text en https://creativecommons.org/licenses/by-nc-nd/4.0/This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which allows reusers to copy and distribute the material in any medium or format in unadapted form only, for noncommercial purposes only, and only so long as attribution is given to the creator. |
spellingShingle | Article He, Ling Ioannidis, Angeliki Arambula, Evelyn Hoffman, Carter J. Joshi, Purva Kathiravan, Anoushka Whitelegge, Julian Liau, Linda M. Kornblum, Harley I. Pajonk, Frank Activation of the mevalonate pathway in response to anti-cancer treatments drives glioblastoma recurrences through activation of Rac-1 |
title | Activation of the mevalonate pathway in response to anti-cancer treatments drives glioblastoma recurrences through activation of Rac-1 |
title_full | Activation of the mevalonate pathway in response to anti-cancer treatments drives glioblastoma recurrences through activation of Rac-1 |
title_fullStr | Activation of the mevalonate pathway in response to anti-cancer treatments drives glioblastoma recurrences through activation of Rac-1 |
title_full_unstemmed | Activation of the mevalonate pathway in response to anti-cancer treatments drives glioblastoma recurrences through activation of Rac-1 |
title_short | Activation of the mevalonate pathway in response to anti-cancer treatments drives glioblastoma recurrences through activation of Rac-1 |
title_sort | activation of the mevalonate pathway in response to anti-cancer treatments drives glioblastoma recurrences through activation of rac-1 |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10402033/ https://www.ncbi.nlm.nih.gov/pubmed/37546917 http://dx.doi.org/10.1101/2023.07.23.550205 |
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