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Effect of low frequency magnetic fields on melanoma: tumor inhibition and immune modulation

BACKGROUND: We previously found that the low frequency magnetic fields (LF-MF) inhibited gastric and lung cancer cell growth. We suppose that exposure to LF-MF may modulate immune function so as to inhibit tumor. We here investigated whether LF-MF can inhibit the proliferation and metastasis of mela...

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Autores principales: Nie, Yunzhong, Du, Leilei, Mou, Yongbin, Xu, Zhenjun, Weng, Leihua, Du, Youwei, Zhu, Yanan, Hou, Yayi, Wang, Tingting
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4029221/
https://www.ncbi.nlm.nih.gov/pubmed/24314291
http://dx.doi.org/10.1186/1471-2407-13-582
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author Nie, Yunzhong
Du, Leilei
Mou, Yongbin
Xu, Zhenjun
Weng, Leihua
Du, Youwei
Zhu, Yanan
Hou, Yayi
Wang, Tingting
author_facet Nie, Yunzhong
Du, Leilei
Mou, Yongbin
Xu, Zhenjun
Weng, Leihua
Du, Youwei
Zhu, Yanan
Hou, Yayi
Wang, Tingting
author_sort Nie, Yunzhong
collection PubMed
description BACKGROUND: We previously found that the low frequency magnetic fields (LF-MF) inhibited gastric and lung cancer cell growth. We suppose that exposure to LF-MF may modulate immune function so as to inhibit tumor. We here investigated whether LF-MF can inhibit the proliferation and metastasis of melanoma and influence immune function. METHODS: The effect of MF on the proliferation, cell cycle and ultrastracture of B16-F10 in vitro was detected by cell counting Kit-8 assay, flow cytometry, and transmission electron microscopy. Lung metastasis mice were prepared by injection of 2 × 10(5) B16-F10 melanoma cells into the tail vein in C57BL/6 mice. The mice were then exposed to an LF-MF (0.4 T, 7.5 Hz) for 43 days. Survival rate, tumor markers and the innate and adaptive immune parameters were measured. RESULTS: The growth of B16-F10 cells was inhibited after exposure to the LF-MF. The inhibition was related to induction of cell cycle arrest and decomposition of chromatins. Moreover, the LF-MF prolonged the mouse survival rate and inhibited the proliferation of B16-F10 in melanoma metastasis mice model. Furthermore, the LF-MF modulated the immune response via regulation of immune cells and cytokine production. In addition, the number of Treg cells was decreased in mice with the LF-MF exposure, while the numbers of T cells as well as dendritic cells were significantly increased. CONCLUSION: LF-MF inhibited the growth and metastasis of melanoma cancer cells and improved immune function of tumor-bearing mice. This suggests that the inhibition may be attributed to modulation of LF-MF on immune function and LF-MF may be a potential therapy for treatment of melanoma.
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spelling pubmed-40292212014-05-22 Effect of low frequency magnetic fields on melanoma: tumor inhibition and immune modulation Nie, Yunzhong Du, Leilei Mou, Yongbin Xu, Zhenjun Weng, Leihua Du, Youwei Zhu, Yanan Hou, Yayi Wang, Tingting BMC Cancer Research Article BACKGROUND: We previously found that the low frequency magnetic fields (LF-MF) inhibited gastric and lung cancer cell growth. We suppose that exposure to LF-MF may modulate immune function so as to inhibit tumor. We here investigated whether LF-MF can inhibit the proliferation and metastasis of melanoma and influence immune function. METHODS: The effect of MF on the proliferation, cell cycle and ultrastracture of B16-F10 in vitro was detected by cell counting Kit-8 assay, flow cytometry, and transmission electron microscopy. Lung metastasis mice were prepared by injection of 2 × 10(5) B16-F10 melanoma cells into the tail vein in C57BL/6 mice. The mice were then exposed to an LF-MF (0.4 T, 7.5 Hz) for 43 days. Survival rate, tumor markers and the innate and adaptive immune parameters were measured. RESULTS: The growth of B16-F10 cells was inhibited after exposure to the LF-MF. The inhibition was related to induction of cell cycle arrest and decomposition of chromatins. Moreover, the LF-MF prolonged the mouse survival rate and inhibited the proliferation of B16-F10 in melanoma metastasis mice model. Furthermore, the LF-MF modulated the immune response via regulation of immune cells and cytokine production. In addition, the number of Treg cells was decreased in mice with the LF-MF exposure, while the numbers of T cells as well as dendritic cells were significantly increased. CONCLUSION: LF-MF inhibited the growth and metastasis of melanoma cancer cells and improved immune function of tumor-bearing mice. This suggests that the inhibition may be attributed to modulation of LF-MF on immune function and LF-MF may be a potential therapy for treatment of melanoma. BioMed Central 2013-12-06 /pmc/articles/PMC4029221/ /pubmed/24314291 http://dx.doi.org/10.1186/1471-2407-13-582 Text en Copyright © 2013 Nie et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Nie, Yunzhong
Du, Leilei
Mou, Yongbin
Xu, Zhenjun
Weng, Leihua
Du, Youwei
Zhu, Yanan
Hou, Yayi
Wang, Tingting
Effect of low frequency magnetic fields on melanoma: tumor inhibition and immune modulation
title Effect of low frequency magnetic fields on melanoma: tumor inhibition and immune modulation
title_full Effect of low frequency magnetic fields on melanoma: tumor inhibition and immune modulation
title_fullStr Effect of low frequency magnetic fields on melanoma: tumor inhibition and immune modulation
title_full_unstemmed Effect of low frequency magnetic fields on melanoma: tumor inhibition and immune modulation
title_short Effect of low frequency magnetic fields on melanoma: tumor inhibition and immune modulation
title_sort effect of low frequency magnetic fields on melanoma: tumor inhibition and immune modulation
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4029221/
https://www.ncbi.nlm.nih.gov/pubmed/24314291
http://dx.doi.org/10.1186/1471-2407-13-582
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