Effect of changing the alternating electric current frequency on the viability of human liver cancer cell line (HEPG2)

Moataz M. Fahmy , Sohier M. El-Kholey , Seham Elabd , Mamdouh M. Shawki

AIMS Biophysics ›› 2025, Vol. 12 ›› Issue (1) : 1 -13.

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AIMS Biophysics ›› 2025, Vol. 12 ›› Issue (1) :1 -13. DOI: 10.3934/biophy.2025001
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Effect of changing the alternating electric current frequency on the viability of human liver cancer cell line (HEPG2)
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Abstract

Different effects of alternating electric currents (AC) on biological materials have been observed depending on the frequency used. Extremely low frequencies (less than 1 KHz) produce electro-endocytosis at 500 Hz because of membrane depolarization. Intermediate frequencies coincide with tiny particle alignments and cell rotations (also known as the pearl chain effect), thus leading to the tumor-treating fields at 100–300 KHz. High frequencies (i.e., above several MHz) cause tissue heating to predominate due to the dielectric losses. This study investigates how exposure to a wide range of AC electric field frequencies affects the permeability and viability of hepatocellular carcinoma HEPG2 cells. With two silver/silver chloride electrodes, the cells were exposed to a square pulse with a magnitude of 0.4 V/cm at various frequencies between 1 Hz and 1 MHz. A dielectric properties measurement, flow cytometry analysis, fluorescent microscopy, and a polymerase chain reaction (PCR) gene expression analysis were performed. The results showed that all the exposed groups experienced a great reduction in the normal cells, with a clear increase in necrosis and apoptosis compared to the control group. It was noticed that the anti-tumoral effect of the examined frequency range was maximum at 10 KHz and 100 KHz. The permeability was increased in the groups exposed to frequencies above 1 kHz. The viability and permeability results were correlated to the electric relative permittivity, electric conductivity, and gene expression of cyclins A, B, and E.

Keywords

electric field frequency / hepatocellular carcinoma HEPG2 / dielectric properties / cell viability / cell permeability

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Moataz M. Fahmy, Sohier M. El-Kholey, Seham Elabd, Mamdouh M. Shawki. Effect of changing the alternating electric current frequency on the viability of human liver cancer cell line (HEPG2). AIMS Biophysics, 2025, 12 (1) : 1-13 DOI:10.3934/biophy.2025001

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References

[1]

Llovet JM, Kelley RK, Villanueva A, et al. (2021) Hepatocellular carcinoma. Nat Rev Dis Primers 7: 6. https://doi.org/10.1038/s41572-020-00240-3

[2]

Bray F, Ferlay J, Soerjomataram I, et al. (2018) Global cancer statistics 2018: GLOBOCAN estimates of incidence and mortality worldwide for 36 cancers in 185 countries. CA Cancer J Clin 68: 394-424. https://doi.org/10.3322/caac.21492

[3]

Marrero JA, Laura MK, Claude BS, et al. (2018) Diagnosis, staging, and management of hepatocellular carcinoma: 2018 practice guidance by the American Association for the Study of Liver Diseases. Hepatology 68: 723-750. https://doi.org/10.1002/hep.29913

[4]

Villemejane J, Mir LM (2009) Physical methods of nucleic acid transfer: general concepts and applications. Br J Pharmacol 157: 207-219. https://doi.org/10.1111/j.1476-5381.2009.00032.x

[5]

Kirson ED, Gurvich Z, Schneiderman R., et al. (2004) Disruption of cancer cell replication by alternating electric fields. Cancer Res 64: 3288-3295. https://doi.org/10.1158/0008-5472.CAN-04-0083

[6]

Zhang Y, Liang H, Tan H, et al. (2020) Development of microfluidic platform to high-throughput quantify single-cell intrinsic bioelectrical markers of tumor cell lines, subtypes and patient tumor cells. Sensor Actuat B-Chem 317: 128231. https://doi.org/10.1016/j.snb.2020.128231

[7]

Cone D (1971) Unified theory on the basic mechanism of normal mitotic control and oncogenesis. J Theor Biol 30: 151-181. https://doi.org/10.1016/0022-5193(71)90042-7

[8]

Al Ahmad M, Al Natour Z, Mustafa F, et al. (2018) Electrical characterization of normal and cancer cells. IEEE Access 6: 25979-25986. https://doi.org/10.1109/ACCESS.2018.2830883

[9]

Manatunga DC, De Silva RM, Nalin KM, et al. (2018) Effective delivery of hydrophobic drugs to breast (MCF-7) and Liver (HepG2) cancer cells: a detailed investigation using cytotoxicity assays, fluorescence imaging and flow cytometry. Eur J Pharm Biopharm 128: 18-26. https://doi.org/10.1016/j.ejpb.2018.04.001

[10]

Tummala V, Jaiswal J, Singh AK, et al. (2022) Biosynthesized silver nanoparticles having high redox current enhance anticancer response for HepG2 cells. Iran J Sci Technol Trans Sci 46: 1531-1539. https://doi.org/10.1007/s40995-022-01374-7

[11]

Kadri K (2019) Polymerase chain reaction (PCR): principle and applications in: perspectives on polymerase chain reaction, Synthetic Biology, New Interdisciplinary Science. https://doi.org/10.5772/intechopen.86491

[12]

Bustin SA, Benes V, Nolan T, et al. (2005) Quantitative real-time RT-PCR-a perspective, J Mol Endocrinol. 34: 597-601. https://doi.org/10.1677/jme.1.01755

[13]

Ambujakshi NP, Raveesha HR, Manohara SR, et al. (2019) Chonemorpha grandiflora extract mediated synthesis of Ag-ZnO nanoparticles for its anticancer, electrical and dielectric applications. Mater Res Express 6: 095068. https://doi.org/10.1088/2053-1591/ab3022

[14]

Camué Ciria HM, González MM, Zamora Lo, et al. (2013) Antitumor effects of electrochemical treatment. Chin J Cancer Res 25: 223-234. do https://10.3978/j.issn.1000-9604.2013.03.03

[15]

Morozas A, Malyško-Ptašinskė V, Kulbacka J, et al. (2024) Electrochemotherapy for head and neck cancers: possibilities and limitations. Front Oncol 14: 1353800. https://doi.org/10.3389/fonc.2024.1353800

[16]

Abd-Elghany AA (2022) Incorporation of electroendocytosis and nanosecond pulsed electric field in electrochemotherapy of breast cancer cells. Electromagn Biol Med 41: 25-34. https://doi.org/10.1080/15368378.2021.1978479

[17]

Prabhakar P, Avudaiappan AP, Sandman M, et al. (2024) Irreversible electroporation as a focal therapy for localized prostate cancer: a systematic review. Indian J Urol 40: 6-16. https://doi.org/10.4103/iju.iju_370_23

[18]

Mun EJ, Babiker HM, Weinberg U, et al. (2018) Tumor-treating fields: a fourth modality in cancer treatment. Clin Cancer Res 24: 266-275. https://doi.org/10.1158/1078-0432.CCR-17-1117

[19]

Giladi M, Weinberg U, Schneiderman RS, et al. (2014) Alternating electric fields (tumor-treating fields therapy) can improve chemotherapy treatment efficacy in non-small cell lung cancer both in vitro and in vivo. Semin Oncol 41: S35-S41. https://doi.org/10.1053/j.seminoncol.2014.09.006

[20]

Xiao D, Yao C, Liu H, et al. (2013) Irreversible electroporation and apoptosis in human liver cancer cells induced by nanosecond electric pulses. Bioelectromagnetics 34: 512-520. https://doi.org/10.1002/bem.21796

[21]

Jing BW, Wen Q, Zhuo Y, et al. (2022) Optimization of three-dimensional culture conditions of HepG2 cells with response surface methodology based on the VitroGel system. Biomed Env Sci 35: 688-698. https://doi.org/10.3967/bes2022.091

[22]

El-Aouar RA, Nicolas A, De Paula TL, et al. (2017) Heterogeneous family of cyclomodulins: smart weapons that allow bacteria to hijack the eukaryotic cell cycle and promote infections. Front Cell Infect Microbiol 7: 208. https://doi.org/10.3389/fcimb.2017.00208

[23]

Xu J, Huang F, Yao Z, et al. (2019) Inhibition of cyclin E1 sensitizes hepatocellular carcinoma cells to regorafenib by mcl-1 suppression. Cell Commun Signal 17: 85. https://doi.org/10.1186/s12964-019-0398-3

[24]

Sonntag R, Penners C, Kohlhepp M, et al. (2021) Cyclin E1 in murine and human liver cancer: a promising target for therapeutic intervention during tumour progression. Cancers (Basel) 13: 5680. https://doi.org/10.3390/cancers13225680

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