Disruption of Cancer Cell Replication by Alternating Electric Fields

Нарушение репликации раковых клеток переменными электрическими полями
Eilon D. Kirson, Zoya Gurvich, Rosa S. Schneiderman, E. Dekel, Aviran Itzhaki, Yoram Wasserman, Rachel Schatzberger, Yoram Palti
2004-05-01

alternating electric fieldsmitotic spindle disruptionnonthermal cancer therapysyngeneic tumor modelstumor cell proliferation
Low-intensity, intermediate-frequency (100-300 kHz), alternating electric fields, delivered by means of insulated electrodes, were found to have a profound inhibitory effect on the growth rate of a variety of human and rodent tumor cell lines (Patricia C, U-118, U-87, H-1299, MDA231, PC3, B16F1, F-98, C-6, RG2, and CT-26) and malignant tumors in animals. This effect, shown to be nonthermal, selectively affects dividing cells while quiescent cells are left intact. These fields act in two modes: arrest of cell proliferation and destruction of cells while undergoing division. Both effects are demonstrated when such fields are applied for 24 h to cells undergoing mitosis that is oriented roughly along the field direction. The first mode of action is manifested by interference with the proper formation of the mitotic spindle, whereas the second results in rapid disintegration of the dividing cells. Both effects, which are frequency dependent, are consistent with the computed directional forces exerted by these specific fields on charges and dipoles within the dividing cells. In vivo treatment of tumors in C57BL/6 and BALB/c mice (B16F1 and CT-26 syngeneic tumor models, respectively), resulted in significant slowing of tumor growth and extensive destruction of tumor cells within 3-6 days. These findings demonstrate the potential applicability of the described electric fields as a novel therapeutic modality for malignant tumors.
1
Electric fields both arrest proliferation by disrupting mitotic-spindle formation and rapidly destroy cells during division.
2
Low-intensity, 100–300 kHz alternating electric fields profoundly inhibit growth across multiple human and rodent tumor cell lines.
3
The nonthermal effect selectively targets dividing cells, while quiescent cells remain intact.
4
These effects are frequency dependent and consistent with directional forces acting on charges and dipoles within dividing cells.
5
Treatment slowed B16F1 and CT-26 tumor growth significantly and caused extensive tumor-cell destruction in mice within 3–6 days.

Human and rodent tumor cells and malignant tumors exposed to low-intensity intermediate-frequency alternating electric fields

The nonthermal, frequency-dependent inhibition and destruction of dividing cancer cells, including mitotic-spindle disruption and tumor-growth suppression

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2004-05-01
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Authors
Eilon D. Kirson
Zoya Gurvich
Rosa S. Schneiderman
E. Dekel
Aviran Itzhaki
Yoram Wasserman
Rachel Schatzberger
Yoram Palti
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