Cell type- and density-dependent effect of 1 T static magnetic field on cell proliferation

Oncotarget. 2017 Feb 21;8(8):13126-13141. doi: 10.18632/oncotarget.14480.

Abstract

Increasing evidence shows that static magnetic fields (SMFs) can affect cell proliferation but mixed results have been reported. Here we systematically examined the effects of 1 T (Tesla) SMF, which is close to the SMF intensity that patients are exposed to MRI (magnetic resonance imaging) scanners in hospitals, for its effect on 15 different cell lines, including 12 human and 3 rodent cell lines. Our results show that 1 T SMF does not have apparent impact on cell cycle or cell death. However, at higher cell density, it reduced cell numbers in six out of seven solid human cancer cell lines. We found that both cell type and cell density had evident impacts on SMF effects. Moreover, the EGFR-Akt-mTOR pathway, which varies significantly between different cell types and densities, contributes to the differential effects of SMF. In addition, SMF also increases the efficacy of Akt inhibitors on cancer cell growth inhibition. Therefore 1 T SMF affects cell proliferation in a cell type- and cell density-dependent manner, and the inhibition effect of 1 T SMF on multiple cancer cells at higher cell density may indicate its clinical potential in late stage cancer therapy.

Keywords: EGFR; cancer cell; static magnetic field.

MeSH terms

  • A549 Cells
  • Animals
  • Antineoplastic Agents / pharmacology
  • Blotting, Western
  • CHO Cells
  • Cell Count*
  • Cell Line
  • Cell Line, Tumor
  • Cell Proliferation*
  • Cricetinae
  • Cricetulus
  • ErbB Receptors / antagonists & inhibitors
  • ErbB Receptors / metabolism
  • HCT116 Cells
  • HEK293 Cells
  • Heterocyclic Compounds, 3-Ring / pharmacology
  • Humans
  • Imidazoles / pharmacology
  • MCF-7 Cells
  • Magnetic Fields*
  • Magnetic Resonance Imaging / methods*
  • Mice
  • NIH 3T3 Cells
  • Protein Kinase Inhibitors / pharmacology
  • Proto-Oncogene Proteins c-akt / antagonists & inhibitors
  • Proto-Oncogene Proteins c-akt / metabolism
  • Quinolines / pharmacology
  • Signal Transduction / drug effects

Substances

  • Antineoplastic Agents
  • Heterocyclic Compounds, 3-Ring
  • Imidazoles
  • MK 2206
  • Protein Kinase Inhibitors
  • Quinolines
  • ErbB Receptors
  • Proto-Oncogene Proteins c-akt
  • dactolisib