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High linear energy transfer carbon-ion irradiation increases the release of the immune mediator high mobility group box 1 from human cancer cells

Anti-tumor immunity modulates the local effects of radiation therapy. High mobility group box 1 (HMGB1) plays a pivotal role in activating antigen-specific T-cell responses. Here, we examined the relationship between linear energy transfer (LET) and HMGB1 release. We assessed the proportions of KYSE...

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Autores principales: Onishi, Masahiro, Okonogi, Noriyuki, Oike, Takahiro, Yoshimoto, Yuya, Sato, Hiro, Suzuki, Yoshiyuki, Kamada, Tadashi, Nakano, Takashi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6151640/
https://www.ncbi.nlm.nih.gov/pubmed/29947767
http://dx.doi.org/10.1093/jrr/rry049
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author Onishi, Masahiro
Okonogi, Noriyuki
Oike, Takahiro
Yoshimoto, Yuya
Sato, Hiro
Suzuki, Yoshiyuki
Kamada, Tadashi
Nakano, Takashi
author_facet Onishi, Masahiro
Okonogi, Noriyuki
Oike, Takahiro
Yoshimoto, Yuya
Sato, Hiro
Suzuki, Yoshiyuki
Kamada, Tadashi
Nakano, Takashi
author_sort Onishi, Masahiro
collection PubMed
description Anti-tumor immunity modulates the local effects of radiation therapy. High mobility group box 1 (HMGB1) plays a pivotal role in activating antigen-specific T-cell responses. Here, we examined the relationship between linear energy transfer (LET) and HMGB1 release. We assessed the proportions of KYSE-70, HeLa and SiHa cells surviving after carbon-ion (C-ion) beam irradiation with different LET values, using a clonogenic assay. The D(10), the dose at which 10% of cells survived, was calculated using a linear–quadratic model. HMGB1 levels in the culture supernatants of C-ion beam–irradiated tumor cells were assessed by enzyme-linked immunosorbent assay. The D(10) doses for 13 keV/μm of C-ion irradiation in KYSE-70, HeLa and SiHa cells were 2.8, 3.9 and 4.1 Gy, respectively, whereas those for 70 keV/μm C-ion irradiation were 1.4, 1.9 and 2.3 Gy, respectively. We found that 70 keV/μm of C-ion irradiation significantly increased HMGB1 levels in the culture supernatants of all cell lines 72 h after irradiation compared with non-irradiated controls. Furthermore, 70 keV/μm of C-ion irradiation significantly increased HMGB1 levels in the culture supernatants of all cell lines 72 h after irradiation compared with 13 keV/μm. The results suggest that HMGB1 release from several cancer cell lines increases with increased LET.
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spelling pubmed-61516402018-09-27 High linear energy transfer carbon-ion irradiation increases the release of the immune mediator high mobility group box 1 from human cancer cells Onishi, Masahiro Okonogi, Noriyuki Oike, Takahiro Yoshimoto, Yuya Sato, Hiro Suzuki, Yoshiyuki Kamada, Tadashi Nakano, Takashi J Radiat Res Regular Paper Anti-tumor immunity modulates the local effects of radiation therapy. High mobility group box 1 (HMGB1) plays a pivotal role in activating antigen-specific T-cell responses. Here, we examined the relationship between linear energy transfer (LET) and HMGB1 release. We assessed the proportions of KYSE-70, HeLa and SiHa cells surviving after carbon-ion (C-ion) beam irradiation with different LET values, using a clonogenic assay. The D(10), the dose at which 10% of cells survived, was calculated using a linear–quadratic model. HMGB1 levels in the culture supernatants of C-ion beam–irradiated tumor cells were assessed by enzyme-linked immunosorbent assay. The D(10) doses for 13 keV/μm of C-ion irradiation in KYSE-70, HeLa and SiHa cells were 2.8, 3.9 and 4.1 Gy, respectively, whereas those for 70 keV/μm C-ion irradiation were 1.4, 1.9 and 2.3 Gy, respectively. We found that 70 keV/μm of C-ion irradiation significantly increased HMGB1 levels in the culture supernatants of all cell lines 72 h after irradiation compared with non-irradiated controls. Furthermore, 70 keV/μm of C-ion irradiation significantly increased HMGB1 levels in the culture supernatants of all cell lines 72 h after irradiation compared with 13 keV/μm. The results suggest that HMGB1 release from several cancer cell lines increases with increased LET. Oxford University Press 2018-09 2018-06-27 /pmc/articles/PMC6151640/ /pubmed/29947767 http://dx.doi.org/10.1093/jrr/rry049 Text en © The Author(s) 2018. Published by Oxford University Press on behalf of The Japan Radiation Research Society and Japanese Society for Radiation Oncology. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Regular Paper
Onishi, Masahiro
Okonogi, Noriyuki
Oike, Takahiro
Yoshimoto, Yuya
Sato, Hiro
Suzuki, Yoshiyuki
Kamada, Tadashi
Nakano, Takashi
High linear energy transfer carbon-ion irradiation increases the release of the immune mediator high mobility group box 1 from human cancer cells
title High linear energy transfer carbon-ion irradiation increases the release of the immune mediator high mobility group box 1 from human cancer cells
title_full High linear energy transfer carbon-ion irradiation increases the release of the immune mediator high mobility group box 1 from human cancer cells
title_fullStr High linear energy transfer carbon-ion irradiation increases the release of the immune mediator high mobility group box 1 from human cancer cells
title_full_unstemmed High linear energy transfer carbon-ion irradiation increases the release of the immune mediator high mobility group box 1 from human cancer cells
title_short High linear energy transfer carbon-ion irradiation increases the release of the immune mediator high mobility group box 1 from human cancer cells
title_sort high linear energy transfer carbon-ion irradiation increases the release of the immune mediator high mobility group box 1 from human cancer cells
topic Regular Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6151640/
https://www.ncbi.nlm.nih.gov/pubmed/29947767
http://dx.doi.org/10.1093/jrr/rry049
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