Cargando…
Radiation quality effects alteration in COX-2 pathway to trigger radiation-induced bystander response in A549 lung carcinoma cells
This study aimed to determine whether the radiation-induced bystander effect (RIBE) is affected by radiation quality. To mimic the different radiation qualities of the direct action (D)/indirect action (ID) ratio, A549 cells were exposed to X-rays, with either 100 mM of the radical scavenger, thio-u...
Autores principales: | , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2018
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6251420/ https://www.ncbi.nlm.nih.gov/pubmed/30124879 http://dx.doi.org/10.1093/jrr/rry065 |
_version_ | 1783373118070325248 |
---|---|
author | Kobayashi, Alisa Konishi, Teruaki |
author_facet | Kobayashi, Alisa Konishi, Teruaki |
author_sort | Kobayashi, Alisa |
collection | PubMed |
description | This study aimed to determine whether the radiation-induced bystander effect (RIBE) is affected by radiation quality. To mimic the different radiation qualities of the direct action (D)/indirect action (ID) ratio, A549 cells were exposed to X-rays, with either 100 mM of the radical scavenger, thio-urea (TU(+)), or null (TU(–)). Biological responses in irradiated and bystander cells were compared at equal lethal effects of a 6% survival dose, which was estimated from the survival curves to be 8 Gy and 5 Gy for TU(+) and TU(–), respectively. Cyclooxygenase-2 (COX-2) expression in TU(–) irradiated cells increased up to 8 h post-irradiation, before decreasing towards 24 h. The concentration of prostaglandin E2 (PGE(2)), a primary product of COX-2 and known as a secreted inducible factor in RIBE, increased over 3-fold compared with that in the control at 8 h post-irradiation. Conversely, COX-2 expression and PGE(2) production of TU(+) irradiated cells were drastically suppressed. These results show that the larger D/ID suppressed COX-2 expression and PGE(2) production in irradiated cells. However, in contrast to the case in the irradiated cells, COX-2 expression was equally observed in the TU(–) and TU(+) co-cultured bystander cells, which showed the highest expression levels at 24 h post-irradiation. Taken together, these findings demonstrate that radiation quality, such as the D/ID ratio, may be an important factor in the alteration of signalling pathways involved in RIBE. |
format | Online Article Text |
id | pubmed-6251420 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-62514202018-11-28 Radiation quality effects alteration in COX-2 pathway to trigger radiation-induced bystander response in A549 lung carcinoma cells Kobayashi, Alisa Konishi, Teruaki J Radiat Res Short Communication This study aimed to determine whether the radiation-induced bystander effect (RIBE) is affected by radiation quality. To mimic the different radiation qualities of the direct action (D)/indirect action (ID) ratio, A549 cells were exposed to X-rays, with either 100 mM of the radical scavenger, thio-urea (TU(+)), or null (TU(–)). Biological responses in irradiated and bystander cells were compared at equal lethal effects of a 6% survival dose, which was estimated from the survival curves to be 8 Gy and 5 Gy for TU(+) and TU(–), respectively. Cyclooxygenase-2 (COX-2) expression in TU(–) irradiated cells increased up to 8 h post-irradiation, before decreasing towards 24 h. The concentration of prostaglandin E2 (PGE(2)), a primary product of COX-2 and known as a secreted inducible factor in RIBE, increased over 3-fold compared with that in the control at 8 h post-irradiation. Conversely, COX-2 expression and PGE(2) production of TU(+) irradiated cells were drastically suppressed. These results show that the larger D/ID suppressed COX-2 expression and PGE(2) production in irradiated cells. However, in contrast to the case in the irradiated cells, COX-2 expression was equally observed in the TU(–) and TU(+) co-cultured bystander cells, which showed the highest expression levels at 24 h post-irradiation. Taken together, these findings demonstrate that radiation quality, such as the D/ID ratio, may be an important factor in the alteration of signalling pathways involved in RIBE. Oxford University Press 2018-11 2018-08-14 /pmc/articles/PMC6251420/ /pubmed/30124879 http://dx.doi.org/10.1093/jrr/rry065 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 | Short Communication Kobayashi, Alisa Konishi, Teruaki Radiation quality effects alteration in COX-2 pathway to trigger radiation-induced bystander response in A549 lung carcinoma cells |
title | Radiation quality effects alteration in COX-2 pathway to trigger radiation-induced bystander response in A549 lung carcinoma cells |
title_full | Radiation quality effects alteration in COX-2 pathway to trigger radiation-induced bystander response in A549 lung carcinoma cells |
title_fullStr | Radiation quality effects alteration in COX-2 pathway to trigger radiation-induced bystander response in A549 lung carcinoma cells |
title_full_unstemmed | Radiation quality effects alteration in COX-2 pathway to trigger radiation-induced bystander response in A549 lung carcinoma cells |
title_short | Radiation quality effects alteration in COX-2 pathway to trigger radiation-induced bystander response in A549 lung carcinoma cells |
title_sort | radiation quality effects alteration in cox-2 pathway to trigger radiation-induced bystander response in a549 lung carcinoma cells |
topic | Short Communication |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6251420/ https://www.ncbi.nlm.nih.gov/pubmed/30124879 http://dx.doi.org/10.1093/jrr/rry065 |
work_keys_str_mv | AT kobayashialisa radiationqualityeffectsalterationincox2pathwaytotriggerradiationinducedbystanderresponseina549lungcarcinomacells AT konishiteruaki radiationqualityeffectsalterationincox2pathwaytotriggerradiationinducedbystanderresponseina549lungcarcinomacells |