[Extremely low frequency electromagnetic field induces apoptosis of osteosarcoma cells via oxidative stress].
← Research streamExposure of MG-63 cells to 50 Hz, 1 mT ELF-EMF for 1–3 h decreased cell viability and growth and increased apoptosis and ROS levels. Pretreatment with NAC (ROS inhibitor) or SB203580 (p38MAPK inhibitor) reduced the ELF-EMF–associated apoptosis, and ELF-EMF ex…
Study snapshot
Abstract
OBJECTIVE: To investigate the effects of extremely low frequency electromagnetic field (ELF-EMF) on human osteosarcoma cells and its mechanisms. METHODS: Human osteosarcoma MG-63 cells were exposed to 50 Hz,1 mT ELF-EMF for 1, 2 and 3 h in vitro, with or without pretreatment by reactive oxygen species (ROS) inhibitor N acetylcysteine (NAC) or p38MAPK inhibitor SB203580. The proliferation of MG-63 cells was determined by MTT method; the apoptosis rate and ROS level in MG-63 cells were detected by flow cytometry. The expression of p38MAPK in MG-63 cells was determined by Western blotting. RESULTS: ELF-EMF decreased the viability of MG-63 cells, inhibited cell growth, induced cell apoptosis and increased the level of ROS significantly. The apoptosis rate declined significantly after treatment with ROS inhibitor NAC or p38MAPK inhibitor SB203580. After exposure to ELF-EMF, p38MAPK in MG-63 cells was activated, and the phosphorylation level was also inhibited after treatment with NAC. CONCLUSION: ELF-EMF can induce the apoptosis of MG-63 cells. Increased ROS and p38MAPK activation may be involved in the mechanism.
AI evidence extraction
Structured fields below were generated from the paper’s abstract and metadata to make the evidence easier to inspect. Automated extraction may be incomplete or incorrect; verify important details against the original paper.
Main findings
Exposure of MG-63 cells to 50 Hz, 1 mT ELF-EMF for 1–3 h decreased cell viability and growth and increased apoptosis and ROS levels. Pretreatment with NAC (ROS inhibitor) or SB203580 (p38MAPK inhibitor) reduced the ELF-EMF–associated apoptosis, and ELF-EMF exposure was associated with p38MAPK activation; NAC inhibited p38MAPK phosphorylation.
Outcomes measured
- Cell viability (MTT)
- Cell proliferation/growth
- Apoptosis rate (flow cytometry)
- Reactive oxygen species (ROS) level (flow cytometry)
- p38MAPK expression/activation and phosphorylation (Western blot)
Limitations
- In vitro study in a single human osteosarcoma cell line (MG-63)
- No sample size or replication details reported in the abstract
- Exposure limited to one frequency (50 Hz), one field strength (1 mT), and short durations (1–3 h)
View raw extracted JSON
{
"study_type": "in_vitro",
"exposure": {
"band": "ELF",
"source": null,
"frequency_mhz": 0.05,
"sar_wkg": null,
"duration": "1, 2 and 3 h"
},
"population": "Human osteosarcoma MG-63 cells (cell line)",
"sample_size": null,
"outcomes": [
"Cell viability (MTT)",
"Cell proliferation/growth",
"Apoptosis rate (flow cytometry)",
"Reactive oxygen species (ROS) level (flow cytometry)",
"p38MAPK expression/activation and phosphorylation (Western blot)"
],
"main_findings": "Exposure of MG-63 cells to 50 Hz, 1 mT ELF-EMF for 1–3 h decreased cell viability and growth and increased apoptosis and ROS levels. Pretreatment with NAC (ROS inhibitor) or SB203580 (p38MAPK inhibitor) reduced the ELF-EMF–associated apoptosis, and ELF-EMF exposure was associated with p38MAPK activation; NAC inhibited p38MAPK phosphorylation.",
"effect_direction": "harm",
"limitations": [
"In vitro study in a single human osteosarcoma cell line (MG-63)",
"No sample size or replication details reported in the abstract",
"Exposure limited to one frequency (50 Hz), one field strength (1 mT), and short durations (1–3 h)"
],
"evidence_strength": "low",
"confidence": 0.78,
"peer_reviewed_likely": "yes",
"keywords": [
"extremely low frequency",
"ELF-EMF",
"50 Hz",
"1 mT",
"osteosarcoma",
"MG-63",
"apoptosis",
"oxidative stress",
"ROS",
"p38MAPK",
"N-acetylcysteine",
"SB203580"
],
"suggested_hubs": []
}AI-extracted fields are generated from the abstract and metadata and may be incomplete or incorrect. This material is for informational purposes and is not medical advice.
Identifiers and source
DOI: 10.3785/j.issn.1008-9292.2015.05.13
PubMed: 26350014
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