» Articles » PMID: 37131108

Tumor Treating Fields (TTFields) Increase the Effectiveness of Temozolomide and Lomustine in Glioblastoma Cell Lines

Overview
Journal J Neurooncol
Publisher Springer
Date 2023 May 2
PMID 37131108
Authors
Affiliations
Soon will be listed here.
Abstract

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-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.

Citing Articles

Optimized Methods to Quantify Tumor Treating Fields (TTFields)-Induced Permeabilization of Glioblastoma Cell Membranes.

Martinez-Paniagua M, Khan S, Henning N, Konagalla S, Patel C Methods Protoc. 2025; 8(1).

PMID: 39997634 PMC: 11858626. DOI: 10.3390/mps8010010.


Tumor Treating Fields enhance chemotherapy efficacy by increasing cellular drug uptake and retention in mesothelioma cells.

Amodeo R, Morosi L, Meroni M, Bello E, Timo S, Frapolli R Am J Cancer Res. 2025; 15(1):271-285.

PMID: 39949944 PMC: 11815374. DOI: 10.62347/ODWL5634.


The subventricular zone structure, function and implications for neurological disease.

Li K, Zheng Y, Cai S, Fan Z, Yang J, Liu Y Genes Dis. 2025; 12(3):101398.

PMID: 39935607 PMC: 11810716. DOI: 10.1016/j.gendis.2024.101398.


Association of tumor treating fields (TTFields) therapy with overall survival in newly diagnosed glioblastoma.

Shah S, Nag A, Lucke-Wold B Clin Transl Oncol. 2025; .

PMID: 39893330 DOI: 10.1007/s12094-025-03849-6.


Recent advances in Tumor Treating Fields (TTFields) therapy for glioblastoma.

Khagi S, Kotecha R, Gatson N, Jeyapalan S, Abdullah H, Avgeropoulos N Oncologist. 2024; 30(2).

PMID: 39401002 PMC: 11883162. DOI: 10.1093/oncolo/oyae227.


References
1.
Faraoni I, Graziani G . Role of BRCA Mutations in Cancer Treatment with Poly(ADP-ribose) Polymerase (PARP) Inhibitors. Cancers (Basel). 2018; 10(12). PMC: 6316750. DOI: 10.3390/cancers10120487. View

2.
Singh N, Miner A, Hennis L, Mittal S . Mechanisms of temozolomide resistance in glioblastoma - a comprehensive review. Cancer Drug Resist. 2021; 4:17-43. PMC: 8319838. DOI: 10.20517/cdr.2020.79. View

3.
Stupp R, Wong E, Kanner A, Steinberg D, Engelhard H, Heidecke V . NovoTTF-100A versus physician's choice chemotherapy in recurrent glioblastoma: a randomised phase III trial of a novel treatment modality. Eur J Cancer. 2012; 48(14):2192-202. DOI: 10.1016/j.ejca.2012.04.011. View

4.
Pohling C, Nguyen H, Chang E, Schubert K, Nie Y, Bashkirov V . Current status of the preclinical evaluation of alternating electric fields as a form of cancer therapy. Bioelectrochemistry. 2022; 149:108287. DOI: 10.1016/j.bioelechem.2022.108287. View

5.
Nguyen N, Redfield J, Ballo M, Michael M, Sorenson J, Dibaba D . Identifying the optimal cutoff point for MGMT promoter methylation status in glioblastoma. CNS Oncol. 2021; 10(3):CNS74. PMC: 8461752. DOI: 10.2217/cns-2021-0002. View