[Millimeter wave exposure induces apoptosis in human melanoma A375 cells in vitro]

Ruiting Zhao1, Yonghong Liu1, Sida Liu1

  • 1School of Biomedical Engineering, Southern Medical University, Guangzhou 510515, China.

Abstract

Insights

Millimeter wave (MMW) exposure triggers apoptosis in human melanoma A375 cells by activating caspase-3. This finding suggests MMW could be a potential therapeutic strategy for melanoma treatment.

Area of Science:

  • Biophysics
  • Cell Biology
  • Oncology

Background:

  • Melanoma is an aggressive form of skin cancer with limited treatment options.
  • Millimeter waves (MMW) are non-ionizing electromagnetic radiation with potential biological effects.
  • Understanding MMW's impact on cancer cells is crucial for developing novel therapies.

Purpose of the Study:

  • To investigate the effects of millimeter wave (MMW) exposure on human melanoma A375 cells.
  • To explore the underlying mechanisms of MMW-induced cell death, specifically apoptosis.
  • To determine the role of caspase-3 activation in MMW-mediated apoptosis.

Main Methods:

  • Electromagnetic field calculations were performed to optimize MMW exposure parameters (SAR).
  • Human melanoma A375 cells were exposed to 35.2 GHz MMW for varying durations (15-90 min).
  • Cell viability was assessed using CCK-8 assay, apoptosis by Annexin-V/PI staining, and caspase-3 expression via Western blotting. Caspase-3 inhibitor AC-DEVD-fmk was used to explore its role.

Main Results:

  • MMW exposure significantly inhibited A375 cell viability in a time-dependent manner (P < 0.05).
  • MMW exposure significantly increased apoptosis and caspase-3 expression in a time-dependent manner (P < 0.05).
  • Pretreatment with a caspase-3 inhibitor partially reversed the MMW-induced decrease in cell viability (P < 0.05).

Conclusions:

  • 35.2 GHz millimeter wave irradiation effectively induces apoptosis in human melanoma A375 cells.
  • The mechanism involves the activation of the caspase-3 protein pathway.
  • MMW exposure demonstrates potential as a therapeutic modality for melanoma.

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