Influence of 50 Hz electromagnetic fields in combination with a tumour promoting phorbol ester on protein kinase C and cell cycle in human cells.

Molecular and cellular biochemistry · 2002 · Mixed · Low evidence

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MixedLow evidencePaper 5301

In human amniotic fluid cells, 50 Hz 1 mT EMF alone showed no effect on PKC translocation. With co-exposure to TPA (10–100 nM), EMF produced a significant additive increase in PKC translocation and a small increase in total PKC activity versus TPA alone, whil…

Study snapshot

PublicationMolecular and cellular biochemistry · 2002

Study typein_vitro

Reported directionMixed

Evidence ratingLow

Abstract

It still is an unsolved issue whether exposure to power-line frequency electromagnetic fields (EMF) may promote carcinogenesis and if so whether it does so by influencing the proliferation, the survival, and the differentiation of cells. Since the family of protein kinases C (PKC) takes part in these processes by interacting with signal transduction pathways at several levels including the activation of transcription factors, we evaluated in the present study the effects of exposure of human amniotic fluid cells (AFC) to 50 Hz, 1 mT electromagnetic fields (EMF) alone and in combination with the tumour promoting phorbol ester 12-O-tetradecanoylphorbol 13-acetate (TPA) on the subcellular localization of PKC protein, on PKC enzyme activity, and on the cell cycle distribution. Quantitative analyses of the PKC expression pattern demonstrated the translocation of PKC from the cytosolic to the membrane fraction after exposure to 10, 50, 100 nM, and 1 microM TPA. EMF exposure alone showed no effect on PKC translocation. Co-exposure to 10, 50, and 100 nM TPA and I mT EMF revealed a significant additive effect (25 +/- 50, 66 +/- 29, 22 +/- 50%, respectively) with the most prominent increase at the concentration of 50 nM TPA. At the highest concentration of TPA used (1 microM) no additive effect of EMF could be observed. Data on enzymatic activity indicate that EMF modulate the PKC activity, showing a significant increase of 10 +/- 16% in total PKC activity after co-exposure to 50 nM TPA and 1 mT EMF when compared to 50 nM TPA alone. Flow cytometric analyses showed a transient cell cycle arrest in G0/G1-phase followed by a delayed transit through S-phase in response to TPA, which was, however, not enhanced by co-exposure with EMF. We conclude that in AFC cells TPA at lower concentrations (< or = 100 nM) induces a less than maximum effect on the PKC pathway, which can be enhanced by the applied EMF.

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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.

Study typein_vitro

Effect directionmixed

PopulationHuman amniotic fluid cells (AFC)

Sample sizeNot supplied

ExposureELF

Evidence strengthLowConfidence: 78% · Peer reviewed: yes

Main findings

Outcomes measured

PKC subcellular localization/translocation (cytosolic to membrane fraction)
PKC enzyme activity (total PKC activity)
Cell cycle distribution (G0/G1 arrest, S-phase transit)

Limitations

In vitro study in a single human cell type (AFC)
No exposure duration reported in abstract
Sample size/replicates not reported in abstract
Endpoints are mechanistic (PKC, cell cycle) rather than clinical outcomes

View raw extracted JSON

{
  "study_type": "in_vitro",
  "exposure": {
    "band": "ELF",
    "source": "power-line frequency",
    "frequency_mhz": null,
    "sar_wkg": null,
    "duration": null
  },
  "population": "Human amniotic fluid cells (AFC)",
  "sample_size": null,
  "outcomes": [
    "PKC subcellular localization/translocation (cytosolic to membrane fraction)",
    "PKC enzyme activity (total PKC activity)",
    "Cell cycle distribution (G0/G1 arrest, S-phase transit)"
  ],
  "main_findings": "In human amniotic fluid cells, 50 Hz 1 mT EMF alone showed no effect on PKC translocation. With co-exposure to TPA (10–100 nM), EMF produced a significant additive increase in PKC translocation and a small increase in total PKC activity versus TPA alone, while cell-cycle effects induced by TPA were not enhanced by EMF; no additive EMF effect was observed at 1 µM TPA.",
  "effect_direction": "mixed",
  "limitations": [
    "In vitro study in a single human cell type (AFC)",
    "No exposure duration reported in abstract",
    "Sample size/replicates not reported in abstract",
    "Endpoints are mechanistic (PKC, cell cycle) rather than clinical outcomes"
  ],
  "evidence_strength": "low",
  "confidence": 0.78,
  "peer_reviewed_likely": "yes",
  "keywords": [
    "50 Hz",
    "1 mT",
    "ELF-EMF",
    "power-line frequency",
    "protein kinase C",
    "PKC translocation",
    "TPA",
    "phorbol ester",
    "cell cycle",
    "human amniotic fluid cells",
    "in vitro"
  ],
  "suggested_hubs": [
    {
      "slug": "occupational-exposure",
      "weight": 0.35,
      "reason": "Uses power-line frequency (50 Hz) ELF magnetic field exposure relevant to occupational/power-frequency contexts."
    }
  ]
}

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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: 10.1023/a:1014802005672
PubMed: 12030371

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