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Studies of the interactions between melatonin and 2 Hz, 0.3 mT PEMF on the proliferation and invasion of human breast cancer cells
Author(s) -
Leman Eddy S.,
Sisken Betty F.,
Zimmer Stephen,
Anderson Kimberly W.
Publication year - 2001
Publication title -
bioelectromagnetics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.435
H-Index - 81
eISSN - 1521-186X
pISSN - 0197-8462
DOI - 10.1002/bem.36
Subject(s) - melatonin , metastasis , human breast , cancer cell , breast cancer , cancer , in vitro , cancer research , cell growth , cell culture , medicine , biology , pathology , endocrinology , chemistry , biochemistry , genetics
Abstract Interactions between the hormone melatonin at pharmacological concentrations (10 −3 M) and 2 Hz, 0.3 mT pulsed electromagnetic fields (PEMF) on the proliferation and invasion of human breast cancer cells were studied in vitro. Three types of human breast cancer cells were used in this study: MDA‐MB‐435, MDA‐MB‐231, and MCF‐7. Results showed that cellular growth of MDA‐MB‐231 cells, which were reported to be lowly metastatic, and MCF‐7 cells, which were reported to be nonmetastatic, were both significantly reduced by melatonin regardless of the presence of the field. Results also showed that MDA‐MB‐435 and MDA‐MB‐231 cells were invasive, with MDA‐MB‐231 cells being more invasive than the MDA‐MB‐435 cells for both unexposed and experimental‐PEMF groups. In addition, invasion studies showed that MCF‐7 cells were not invasive and that melatonin did not have any effects on the invasion of these cells, with or without the PEMF. It is also suggested that since metastasis requires growth and invasion into tissue, anti‐invasion agents can be used in conjunction with melatonin to prevent formation of secondary metastases. The overall studies suggest that PEMF at 2 Hz, 0.3 mT does not influence cancer metastasis; while having clinical merit in the healing of soft tissue injury, this field has shown no influence on cancer cells as 60 Hz power line fields have. Bioelectromagnetics 22:178–184, 2001. © 2001 Wiley‐Liss, Inc.