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Efficacy of Juzentaihoto for Tumor Immunotherapy in B16 Melanoma Metastasis Model
Introduction. Medical care for Japanese cancer patients includes Western and Kampo medicines, and treatments with juzentaihoto (JTT) reportedly prevent cancer metastasis and recurrence. In this study, we examined the effects of JTT on natural killer (NK) cell activity and metastasis in combined trea...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi Publishing Corporation
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5329671/ https://www.ncbi.nlm.nih.gov/pubmed/28286532 http://dx.doi.org/10.1155/2017/6054706 |
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author | Ishikawa, Shintaro Ishikawa, Takako Tezuka, Chiaki Asano, Kazuhito Sunagawa, Masataka Hisamitsu, Tadashi |
author_facet | Ishikawa, Shintaro Ishikawa, Takako Tezuka, Chiaki Asano, Kazuhito Sunagawa, Masataka Hisamitsu, Tadashi |
author_sort | Ishikawa, Shintaro |
collection | PubMed |
description | Introduction. Medical care for Japanese cancer patients includes Western and Kampo medicines, and treatments with juzentaihoto (JTT) reportedly prevent cancer metastasis and recurrence. In this study, we examined the effects of JTT on natural killer (NK) cell activity and metastasis in combined treatments with anti-PD-1 antibody in a mouse model of melanoma metastasis. Methods. C57BL/6 male mice were intravenously injected with B16 melanoma cells (B16 cell) and were given chow containing 3% JTT. In subsequent in vivo experiments, we assessed serum cytokine levels and tumor colony formation in the lungs. Additionally, we assessed NK cell activity in ex vivo experiments. Results. JTT significantly suppressed B16 cell metastasis, whereas injection of anti-asialo-GM1 antibody into mice abrogated the inhibitory actions of JTT. JTT significantly increased interleukin- (IL-) 12 and interferon- (IFN-) γ levels in serum and induced NK cell activity. It increased the inhibitory actions of the anti-PD-1 antibody on B16 cell metastasis. Discussion. These data suggest that JTT inhibits B16 cell metastasis by inducing NK cell activity. Additionally, combination therapy with JTT and anti-PD-1 antibody increased treatment response rates for B16 melanoma. |
format | Online Article Text |
id | pubmed-5329671 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Hindawi Publishing Corporation |
record_format | MEDLINE/PubMed |
spelling | pubmed-53296712017-03-12 Efficacy of Juzentaihoto for Tumor Immunotherapy in B16 Melanoma Metastasis Model Ishikawa, Shintaro Ishikawa, Takako Tezuka, Chiaki Asano, Kazuhito Sunagawa, Masataka Hisamitsu, Tadashi Evid Based Complement Alternat Med Research Article Introduction. Medical care for Japanese cancer patients includes Western and Kampo medicines, and treatments with juzentaihoto (JTT) reportedly prevent cancer metastasis and recurrence. In this study, we examined the effects of JTT on natural killer (NK) cell activity and metastasis in combined treatments with anti-PD-1 antibody in a mouse model of melanoma metastasis. Methods. C57BL/6 male mice were intravenously injected with B16 melanoma cells (B16 cell) and were given chow containing 3% JTT. In subsequent in vivo experiments, we assessed serum cytokine levels and tumor colony formation in the lungs. Additionally, we assessed NK cell activity in ex vivo experiments. Results. JTT significantly suppressed B16 cell metastasis, whereas injection of anti-asialo-GM1 antibody into mice abrogated the inhibitory actions of JTT. JTT significantly increased interleukin- (IL-) 12 and interferon- (IFN-) γ levels in serum and induced NK cell activity. It increased the inhibitory actions of the anti-PD-1 antibody on B16 cell metastasis. Discussion. These data suggest that JTT inhibits B16 cell metastasis by inducing NK cell activity. Additionally, combination therapy with JTT and anti-PD-1 antibody increased treatment response rates for B16 melanoma. Hindawi Publishing Corporation 2017 2017-02-12 /pmc/articles/PMC5329671/ /pubmed/28286532 http://dx.doi.org/10.1155/2017/6054706 Text en Copyright © 2017 Shintaro Ishikawa et al. https://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Ishikawa, Shintaro Ishikawa, Takako Tezuka, Chiaki Asano, Kazuhito Sunagawa, Masataka Hisamitsu, Tadashi Efficacy of Juzentaihoto for Tumor Immunotherapy in B16 Melanoma Metastasis Model |
title | Efficacy of Juzentaihoto for Tumor Immunotherapy in B16 Melanoma Metastasis Model |
title_full | Efficacy of Juzentaihoto for Tumor Immunotherapy in B16 Melanoma Metastasis Model |
title_fullStr | Efficacy of Juzentaihoto for Tumor Immunotherapy in B16 Melanoma Metastasis Model |
title_full_unstemmed | Efficacy of Juzentaihoto for Tumor Immunotherapy in B16 Melanoma Metastasis Model |
title_short | Efficacy of Juzentaihoto for Tumor Immunotherapy in B16 Melanoma Metastasis Model |
title_sort | efficacy of juzentaihoto for tumor immunotherapy in b16 melanoma metastasis model |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5329671/ https://www.ncbi.nlm.nih.gov/pubmed/28286532 http://dx.doi.org/10.1155/2017/6054706 |
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