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Radiofrequency Induced Time-Dependent Alterations in Gene Expression and Apoptosis in Glioblastoma Cell Line.

Authors :
Tuysuz MZ
Kayhan H
Saglam ASY
Senturk F
Bagriacik EU
Yagci M
Canseven AG
Source :
Bioelectromagnetics [Bioelectromagnetics] 2025 Jan; Vol. 46 (1), pp. e22543.
Publication Year :
2025

Abstract

The widespread use of wireless communication technologies has increased human exposure to radiofrequency electromagnetic fields (RF-EMFs). Considering the brain's close proximity to mobile phones and its entirely electrical transmission network, it emerges as the organ most profoundly impacted by the RF field. This study aims to investigate the potential effects of RF radiation on cell viability, apoptosis, and gene expressions in glioblastoma cells (U118-MG) at different exposure times (1, 24, and 48 h). To achieve this, we designed and implemented an in vitro RF exposure system operating at a frequency of 2.1 GHz, specifically for cell culture studies, with an average specific absorption rate (SAR) of 1.12 ± 0.18 W/kg determined through numerical dosimetry calculations. Results reveal a significant influence of a 48 h exposure to a 2.1 GHz RF field on U118-MG cell viability, gene expression, and the induction of caspase (CASP) dependent apoptosis. Notably, increased CASP3, CASP8, and CASP9 mRNA levels were observed after 24 and 48 h of RF treatment. However, only the 48 h RF exposure resulted in apoptotic cell death and a significant elevation in the BAX/BCL-2 ratio. This observed effect may be influenced by extended exposure durations surpassing the cell's doubling time. The increased BAX/BCL-2 ratio, which acts as a key switch for apoptosis, and the heterogeneous morphology of the astrocyte-derived U118-MG cell line may also play a role in this effect.<br /> (© 2025 Bioelectromagnetics Society.)

Details

Language :
English
ISSN :
1521-186X
Volume :
46
Issue :
1
Database :
MEDLINE
Journal :
Bioelectromagnetics
Publication Type :
Academic Journal
Accession number :
39810728
Full Text :
https://doi.org/10.1002/bem.22543