EVALUATION OF BCL2 AND ITS REGULATORY MIRS, MIR-15-B AND MIR-16 EXPRESSION CHANGES UNDER THE EXPOSURE OF EXTREMELY LOW-FREQUENCY ELECTROMAGNETIC FIELDS ON HUMAN GASTRIC CANCER CELL LINE.
← Research streamELF-EMF exposure at 2 mT continuous significantly reduced AGS cell viability. BCL2 expression was significantly decreased after continuous exposure at 0.2 and 2 mT and after discontinuous exposure at 2 mT. miR-15-b and miR-16 expression were significantly inc…
Study snapshot
Abstract
In this research, changes in the expression of B-cell lymphoma 2 (BCL2), miR-15-b and miR-16 in human adenocarcinoma gastric cancer cell line (AGS) following the exposure to magnetic flux densities (MFDs) of 0.2 and 2 mT continuously and discontinuously (1.5 h on/1.5 h off) for 18 h were investigated. Changes in the cell viability were evaluated by the MTT assay. Real-time PCR was used to evaluate the expression changes of BCL2, miR-15-b and miR-16. The results showed that extremely low frequency electromagnetic field (ELF-EMF) could significantly reduce the viability of AGS cells in the continuous MFD of 2 mT. The BCL2 expression was significantly decreased following the exposure to continuous MFDs of 0.2 and 2 mT and discontinuous MFD of 2 mT. The expressions of miR-15-b and miR-16 were significantly increased in continuous and discontinuous MFD of 2 mT. According to the results, weak and moderate extremely low-frequency electromagnetic fields can change the expressions of BCL2, miR-15-b and miR-16.
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
ELF-EMF exposure at 2 mT continuous significantly reduced AGS cell viability. BCL2 expression was significantly decreased after continuous exposure at 0.2 and 2 mT and after discontinuous exposure at 2 mT. miR-15-b and miR-16 expression were significantly increased in both continuous and discontinuous 2 mT conditions.
Outcomes measured
- Cell viability (MTT assay)
- BCL2 expression (real-time PCR)
- miR-15-b expression (real-time PCR)
- miR-16 expression (real-time PCR)
Limitations
- Frequency of the ELF-EMF exposure was not reported in the abstract.
- In vitro cancer cell line model; generalizability to humans is not addressed in the abstract.
- Sample size/replicates and detailed dosimetry beyond magnetic flux density are not provided in the abstract.
View raw extracted JSON
{
"study_type": "in_vitro",
"exposure": {
"band": "ELF",
"source": null,
"frequency_mhz": null,
"sar_wkg": null,
"duration": "18 h (continuous or discontinuous 1.5 h on/1.5 h off)"
},
"population": "Human gastric adenocarcinoma cancer cell line (AGS)",
"sample_size": null,
"outcomes": [
"Cell viability (MTT assay)",
"BCL2 expression (real-time PCR)",
"miR-15-b expression (real-time PCR)",
"miR-16 expression (real-time PCR)"
],
"main_findings": "ELF-EMF exposure at 2 mT continuous significantly reduced AGS cell viability. BCL2 expression was significantly decreased after continuous exposure at 0.2 and 2 mT and after discontinuous exposure at 2 mT. miR-15-b and miR-16 expression were significantly increased in both continuous and discontinuous 2 mT conditions.",
"effect_direction": "mixed",
"limitations": [
"Frequency of the ELF-EMF exposure was not reported in the abstract.",
"In vitro cancer cell line model; generalizability to humans is not addressed in the abstract.",
"Sample size/replicates and detailed dosimetry beyond magnetic flux density are not provided in the abstract."
],
"evidence_strength": "low",
"confidence": 0.78,
"peer_reviewed_likely": "yes",
"keywords": [
"ELF-EMF",
"extremely low frequency",
"magnetic flux density",
"0.2 mT",
"2 mT",
"AGS",
"gastric cancer cell line",
"cell viability",
"MTT",
"BCL2",
"miR-15-b",
"miR-16",
"gene expression",
"real-time PCR"
],
"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: 10.1093/rpd/ncab163
PubMed: 34791478
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