Cargando…
Tumor Treating Fields (TTFields) increase the effectiveness of temozolomide and lomustine in glioblastoma cell lines
PURPOSE: Tumor Treating Fields (TTFields) are electric fields that disrupt cellular processes critical for cancer cell viability and tumor progression, ultimately leading to cell death. TTFields therapy is approved for treatment of newly-diagnosed glioblastoma (GBM) concurrent with maintenance temoz...
Autores principales: | , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer US
2023
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10232578/ https://www.ncbi.nlm.nih.gov/pubmed/37131108 http://dx.doi.org/10.1007/s11060-023-04308-4 |
_version_ | 1785052012463783936 |
---|---|
author | Fishman, Hila Monin, Roni Dor-On, Eyal Kinzel, Adrian Haber, Adi Giladi, Moshe Weinberg, Uri Palti, Yoram |
author_facet | Fishman, Hila Monin, Roni Dor-On, Eyal Kinzel, Adrian Haber, Adi Giladi, Moshe Weinberg, Uri Palti, Yoram |
author_sort | Fishman, Hila |
collection | PubMed |
description | PURPOSE: Tumor Treating Fields (TTFields) are electric fields that disrupt cellular processes critical for cancer cell viability and tumor progression, ultimately leading to cell death. TTFields therapy is approved for treatment of newly-diagnosed glioblastoma (GBM) concurrent with maintenance temozolomide (TMZ). Recently, the benefit of TMZ in combination with lomustine (CCNU) was demonstrated in patients with O(6)-methylguanine DNA methyltransferase (MGMT) promoter methylation. The addition of adjuvant TTFields to TMZ plus CCNU further improved patient outcomes, leading to a CE mark for this regimen. The current in vitro study aimed to elucidate the mechanism underlying the benefit of this treatment protocol. METHODS: Human GBM cell lines with different MGMT promoter methylation statuses were treated with TTFields, TMZ, and CCNU, and effectiveness was tested by cell count, apoptosis, colony formation, and DNA damage measurements. Expression levels of relevant DNA-repair proteins were examined by western blot analysis. RESULTS: TTFields concomitant with TMZ displayed an additive effect, irrespective of MGMT expression levels. TTFields concomitant with CCNU or with CCNU plus TMZ was additive in MGMT-expressing cells and synergistic in MGMT-non-expressing cells. TTFields downregulated the FA-BRCA pathway and increased DNA damage induced by the chemotherapy combination. CONCLUSIONS: The results support the clinical benefit demonstrated for TTFields concomitant with TMZ plus CCNU. Since the FA-BRCA pathway is required for repair of DNA cross-links induced by CCNU in the absence of MGMT, the synergy demonstrated in MGMT promoter methylated cells when TTFields and CCNU were co-applied may be attributed to the BRCAness state induced by TTFields. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s11060-023-04308-4. |
format | Online Article Text |
id | pubmed-10232578 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Springer US |
record_format | MEDLINE/PubMed |
spelling | pubmed-102325782023-06-02 Tumor Treating Fields (TTFields) increase the effectiveness of temozolomide and lomustine in glioblastoma cell lines Fishman, Hila Monin, Roni Dor-On, Eyal Kinzel, Adrian Haber, Adi Giladi, Moshe Weinberg, Uri Palti, Yoram J Neurooncol Research PURPOSE: Tumor Treating Fields (TTFields) are electric fields that disrupt cellular processes critical for cancer cell viability and tumor progression, ultimately leading to cell death. TTFields therapy is approved for treatment of newly-diagnosed glioblastoma (GBM) concurrent with maintenance temozolomide (TMZ). Recently, the benefit of TMZ in combination with lomustine (CCNU) was demonstrated in patients with O(6)-methylguanine DNA methyltransferase (MGMT) promoter methylation. The addition of adjuvant TTFields to TMZ plus CCNU further improved patient outcomes, leading to a CE mark for this regimen. The current in vitro study aimed to elucidate the mechanism underlying the benefit of this treatment protocol. METHODS: Human GBM cell lines with different MGMT promoter methylation statuses were treated with TTFields, TMZ, and CCNU, and effectiveness was tested by cell count, apoptosis, colony formation, and DNA damage measurements. Expression levels of relevant DNA-repair proteins were examined by western blot analysis. RESULTS: TTFields concomitant with TMZ displayed an additive effect, irrespective of MGMT expression levels. TTFields concomitant with CCNU or with CCNU plus TMZ was additive in MGMT-expressing cells and synergistic in MGMT-non-expressing cells. TTFields downregulated the FA-BRCA pathway and increased DNA damage induced by the chemotherapy combination. CONCLUSIONS: The results support the clinical benefit demonstrated for TTFields concomitant with TMZ plus CCNU. Since the FA-BRCA pathway is required for repair of DNA cross-links induced by CCNU in the absence of MGMT, the synergy demonstrated in MGMT promoter methylated cells when TTFields and CCNU were co-applied may be attributed to the BRCAness state induced by TTFields. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s11060-023-04308-4. Springer US 2023-05-02 2023 /pmc/articles/PMC10232578/ /pubmed/37131108 http://dx.doi.org/10.1007/s11060-023-04308-4 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open AccessThis 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/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Research Fishman, Hila Monin, Roni Dor-On, Eyal Kinzel, Adrian Haber, Adi Giladi, Moshe Weinberg, Uri Palti, Yoram Tumor Treating Fields (TTFields) increase the effectiveness of temozolomide and lomustine in glioblastoma cell lines |
title | Tumor Treating Fields (TTFields) increase the effectiveness of temozolomide and lomustine in glioblastoma cell lines |
title_full | Tumor Treating Fields (TTFields) increase the effectiveness of temozolomide and lomustine in glioblastoma cell lines |
title_fullStr | Tumor Treating Fields (TTFields) increase the effectiveness of temozolomide and lomustine in glioblastoma cell lines |
title_full_unstemmed | Tumor Treating Fields (TTFields) increase the effectiveness of temozolomide and lomustine in glioblastoma cell lines |
title_short | Tumor Treating Fields (TTFields) increase the effectiveness of temozolomide and lomustine in glioblastoma cell lines |
title_sort | tumor treating fields (ttfields) increase the effectiveness of temozolomide and lomustine in glioblastoma cell lines |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10232578/ https://www.ncbi.nlm.nih.gov/pubmed/37131108 http://dx.doi.org/10.1007/s11060-023-04308-4 |
work_keys_str_mv | AT fishmanhila tumortreatingfieldsttfieldsincreasetheeffectivenessoftemozolomideandlomustineinglioblastomacelllines AT moninroni tumortreatingfieldsttfieldsincreasetheeffectivenessoftemozolomideandlomustineinglioblastomacelllines AT doroneyal tumortreatingfieldsttfieldsincreasetheeffectivenessoftemozolomideandlomustineinglioblastomacelllines AT kinzeladrian tumortreatingfieldsttfieldsincreasetheeffectivenessoftemozolomideandlomustineinglioblastomacelllines AT haberadi tumortreatingfieldsttfieldsincreasetheeffectivenessoftemozolomideandlomustineinglioblastomacelllines AT giladimoshe tumortreatingfieldsttfieldsincreasetheeffectivenessoftemozolomideandlomustineinglioblastomacelllines AT weinberguri tumortreatingfieldsttfieldsincreasetheeffectivenessoftemozolomideandlomustineinglioblastomacelllines AT paltiyoram tumortreatingfieldsttfieldsincreasetheeffectivenessoftemozolomideandlomustineinglioblastomacelllines |