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Tumor Treating Fields Suppression of Ciliogenesis Enhances Temozolomide Toxicity

Tumor Treating Fields (TTFields) are low-intensity, alternating intermediate-frequency (200 kHz) electrical fields that extend survival of glioblastoma patients receiving maintenance temozolomide (TMZ) chemotherapy. How TTFields exert efficacy on cancer over normal cells or interact with TMZ is uncl...

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Autores principales: Shi, Ping, Tian, Jia, Ulm, Brittany S., Mallinger, Julianne C., Khoshbouei, Habibeh, Deleyrolle, Loic P., Sarkisian, Matthew R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8962950/
https://www.ncbi.nlm.nih.gov/pubmed/35359402
http://dx.doi.org/10.3389/fonc.2022.837589
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author Shi, Ping
Tian, Jia
Ulm, Brittany S.
Mallinger, Julianne C.
Khoshbouei, Habibeh
Deleyrolle, Loic P.
Sarkisian, Matthew R.
author_facet Shi, Ping
Tian, Jia
Ulm, Brittany S.
Mallinger, Julianne C.
Khoshbouei, Habibeh
Deleyrolle, Loic P.
Sarkisian, Matthew R.
author_sort Shi, Ping
collection PubMed
description Tumor Treating Fields (TTFields) are low-intensity, alternating intermediate-frequency (200 kHz) electrical fields that extend survival of glioblastoma patients receiving maintenance temozolomide (TMZ) chemotherapy. How TTFields exert efficacy on cancer over normal cells or interact with TMZ is unclear. Primary cilia are microtubule-based organelles triggered by extracellular ligands, mechanical and electrical field stimulation and are capable of promoting cancer growth and TMZ chemoresistance. We found in both low- and high-grade patient glioma cell lines that TTFields ablated cilia within 24 h. Halting TTFields treatment led to recovered frequencies of elongated cilia. Cilia on normal primary astrocytes, neurons, and multiciliated/ependymal cells were less affected by TTFields. The TTFields-mediated loss of glioma cilia was partially rescued by chloroquine pretreatment, suggesting the effect is in part due to autophagy activation. We also observed death of ciliated cells during TTFields by live imaging. Notably, TMZ and TTFields have opposing effects on glioma ciliogenesis. TMZ-induced stimulation of ciliogenesis in both adherent cells and gliomaspheres was blocked by TTFields. Surprisingly, the inhibitory effects of TTFields and TMZ on tumor cell recurrence are linked to the relative timing of TMZ exposure to TTFields and ARL13B(+) cilia. Finally, TTFields disrupted cilia in patient tumors treated ex vivo. Our findings suggest that the efficacy of TTFields may depend on the degree of tumor ciliogenesis and relative timing of TMZ treatment.
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spelling pubmed-89629502022-03-30 Tumor Treating Fields Suppression of Ciliogenesis Enhances Temozolomide Toxicity Shi, Ping Tian, Jia Ulm, Brittany S. Mallinger, Julianne C. Khoshbouei, Habibeh Deleyrolle, Loic P. Sarkisian, Matthew R. Front Oncol Oncology Tumor Treating Fields (TTFields) are low-intensity, alternating intermediate-frequency (200 kHz) electrical fields that extend survival of glioblastoma patients receiving maintenance temozolomide (TMZ) chemotherapy. How TTFields exert efficacy on cancer over normal cells or interact with TMZ is unclear. Primary cilia are microtubule-based organelles triggered by extracellular ligands, mechanical and electrical field stimulation and are capable of promoting cancer growth and TMZ chemoresistance. We found in both low- and high-grade patient glioma cell lines that TTFields ablated cilia within 24 h. Halting TTFields treatment led to recovered frequencies of elongated cilia. Cilia on normal primary astrocytes, neurons, and multiciliated/ependymal cells were less affected by TTFields. The TTFields-mediated loss of glioma cilia was partially rescued by chloroquine pretreatment, suggesting the effect is in part due to autophagy activation. We also observed death of ciliated cells during TTFields by live imaging. Notably, TMZ and TTFields have opposing effects on glioma ciliogenesis. TMZ-induced stimulation of ciliogenesis in both adherent cells and gliomaspheres was blocked by TTFields. Surprisingly, the inhibitory effects of TTFields and TMZ on tumor cell recurrence are linked to the relative timing of TMZ exposure to TTFields and ARL13B(+) cilia. Finally, TTFields disrupted cilia in patient tumors treated ex vivo. Our findings suggest that the efficacy of TTFields may depend on the degree of tumor ciliogenesis and relative timing of TMZ treatment. Frontiers Media S.A. 2022-03-11 /pmc/articles/PMC8962950/ /pubmed/35359402 http://dx.doi.org/10.3389/fonc.2022.837589 Text en Copyright © 2022 Shi, Tian, Ulm, Mallinger, Khoshbouei, Deleyrolle and Sarkisian https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Oncology
Shi, Ping
Tian, Jia
Ulm, Brittany S.
Mallinger, Julianne C.
Khoshbouei, Habibeh
Deleyrolle, Loic P.
Sarkisian, Matthew R.
Tumor Treating Fields Suppression of Ciliogenesis Enhances Temozolomide Toxicity
title Tumor Treating Fields Suppression of Ciliogenesis Enhances Temozolomide Toxicity
title_full Tumor Treating Fields Suppression of Ciliogenesis Enhances Temozolomide Toxicity
title_fullStr Tumor Treating Fields Suppression of Ciliogenesis Enhances Temozolomide Toxicity
title_full_unstemmed Tumor Treating Fields Suppression of Ciliogenesis Enhances Temozolomide Toxicity
title_short Tumor Treating Fields Suppression of Ciliogenesis Enhances Temozolomide Toxicity
title_sort tumor treating fields suppression of ciliogenesis enhances temozolomide toxicity
topic Oncology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8962950/
https://www.ncbi.nlm.nih.gov/pubmed/35359402
http://dx.doi.org/10.3389/fonc.2022.837589
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