Abstract
Transcranial magnetic stimulation (TMS) is a widely available technology employing relatively strong (up to 4 T) pulsed (up to 300 Hz) magnetic fields for diagnostics of brain functions and treatment of various brain disorders. The current paradigm implies that the magnetic induction of Eddy currents in the brain neurons is the leading biological mechanism of TMS. At the same time, it is almost unknown how the TMS-like magnetic fields act on nonneuronal cells. Here, we explored the effects of TMS-like repetitive magnetic stimulation (RMS) on metabolic activity of human colorectal cancer (CRC) and hepatocellular carcinoma (HCC) cells. The HCT116 (CRC) and HuH7 (HCC) in vitro cell cultures were treated using a TMS device 'Magstim Rapid2' with an air-cooled 'Magstim' figure-eight coil (AFC70). Five intermittent RMS (iRMS) and two burst RMS (bRMS) experimental protocols were applied to the monolayers of the cells as a single treatment session. The activity of succinate dehydrogenase, an enzyme essential for energy production in mitochondria, was measured by 3(4,5-dimethylthiazol-2-yl)-2,5-diphenyl tetrazolium bromide (MTT) colorimetric viability assay in 24 h post-stimulation. Compared to untreated control, in HCT116 cells, a low-frequency iRMS treatment ( f = 1 Hz, 600 pulses, B = 0.8 T) induced a statistically significant decrease in metabolic activity (viability), while the high-frequency iRMS and bRMS increased it. In HuH7 cells, all tested RMS protocols either did not change or stimulated the metabolic activity (viability) of the cells, in comparison to the untreated control. The analysis of correlations revealed the almost opposite trends in CRC and HCC cells response to the frequency, temporal patterns, and magnetic field flux density considered as the parameters of the experimental RMS. Our findings demonstrate the tumor type- and stimulation protocol-specific effects of the repurposed TMS technology on colorectal and liver cancer cells. The underlying mechanism of these differences requires further study. The current results indicate that TMS-like magnetic fields may have new potential applications as an adjuvant anticancer treatment modality.
| Original language | English |
|---|---|
| Article number | 5400206 |
| Number of pages | 6 |
| Journal | IEEE Transactions on Magnetics |
| Volume | 58 |
| Issue number | 8 |
| Early online date | 27 Jan 2022 |
| DOIs | |
| Publication status | Published - 1 Aug 2022 |
Keywords
- in vitro cell culture
- repetitive magnetic stimulation (RMS)
- transcranial magnetic stimulation (TMS)
- cancer
- 3(4,5-dimethylthiazol-2-yl)-2,5-diphenyl tetrazolium bromide (MTT) assay
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Dive into the research topics of 'TMS-like magnetic fields modulate metabolic activity of hepatic and colorectal cancer cells'. Together they form a unique fingerprint.Projects
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Biomolecular Discovery and Design Research Centre
Packer, N. (Primary Chief Investigator), Paulsen, I. (Chief Investigator), Nevalainen, H. (Chief Investigator), Haynes, P. (Chief Investigator), Molloy, M. (Chief Investigator), Atwell, B. (Chief Investigator), Barron, A. (Chief Investigator), Beggs, P. (Chief Investigator), Bergquist, P. L. (Chief Investigator), Brown, L. (Chief Investigator), Cornish, J. (Chief Investigator), Chung, R. (Chief Investigator), De Deene, Y. (Chief Investigator), Garcia-Bennett, A. (Chief Investigator), Gillings, M. (Chief Investigator), Goodchild, A. (Chief Investigator), Guillemin, G. (Chief Investigator), Hallinan, J. (Chief Investigator), Hose, G. (Chief Investigator), Jaschke, P. (Chief Investigator), Mabbutt, B. (Chief Investigator), Raftos, D. (Chief Investigator), Ranganathan, S. (Chief Investigator), Sofronov, G. (Chief Investigator), Sunna, A. (Chief Investigator), Tetu, S. (Chief Investigator), Andersen, M. (Chief Investigator), Willows, R. (Chief Investigator), Ahn, C. (Associate Investigator), Breen, E. (Associate Investigator), Campbell, M. (Associate Investigator), Care, A. (Associate Investigator), Cordina, N. (Associate Investigator), Curach, N. (Associate Investigator), Everest Dass, A. (Associate Investigator), Elbourne, L. (Associate Investigator), Goold, H. (Associate Investigator), Hassan, K. (Associate Investigator), Kautto, L. (Associate Investigator), Krisp, C. (Associate Investigator), Kroukamp, H. (Associate Investigator), Lee, A. (Associate Investigator), Lin, C.-H. (Associate Investigator), Mackie, A. (Associate Investigator), McKay, M. (Associate Investigator), McQuade, L. (Associate Investigator), Mirzaei, M. (Associate Investigator), Mohamedali, A. (Associate Investigator), Ostrowski, M. (Associate Investigator), Parker, L. (Associate Investigator), Pascovici, D. (Associate Investigator), Penesyan, A. (Associate Investigator), Shah, B. (Associate Investigator), Sun, A. (Associate Investigator), Thompson, E. (Associate Investigator) & Williams, T. (Associate Investigator)
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Deciphering the kidney matrisome: identification and quantification of renal extracellular matrix proteins in healthy mice
Rende, U., Ahn, S. B., Adhikari, S., Moh, E. S. X., Pollock, C. A., Saad, S. & Guller, A., 1 Feb 2023, In: International Journal of Molecular Sciences. 24, 3, p. 1-31 31 p., 2827.Research output: Contribution to journal › Article › peer-review
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Cells-in-touch: 3D printing in reconstruction and modelling of microscopic biological geometries for research and education
Fitzpatrick, X., Fayzullin, A., Dokos, S. & Guller, A., 10 May 2022, (Submitted) 23 p. (Preprints).Research output: Working paper › Preprint
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Potential anticancer and immunomodulatory effects of TMS magnetic fields
Guller, A., Clement, S., Heng, B., Sowman, P., Guillemin, G. & Goldys, E., Sept 2021, In: Asia-Pacific Journal of Clinical Oncology. 17, (S5), p. 44-45 2 p., 77.Research output: Contribution to journal › Meeting abstract › peer-review
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