Cargando…

Radiation-induced bystander effect in non-irradiated glioblastoma spheroid cells

Radiation-induced bystander effects (RIBEs) are detected in cells that are not irradiated but receive signals from treated cells. The present study explored these bystander effects in a U87MG multicellular tumour spheroid model. A medium transfer technique was employed to induce the bystander effect...

Descripción completa

Detalles Bibliográficos
Autores principales: Faqihi, Fahime, Neshastehriz, Ali, Soleymanifard, Shokouhozaman, Shabani, Robabeh, Eivazzadeh, Nazila
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4577008/
https://www.ncbi.nlm.nih.gov/pubmed/26160180
http://dx.doi.org/10.1093/jrr/rrv039
_version_ 1782390932867383296
author Faqihi, Fahime
Neshastehriz, Ali
Soleymanifard, Shokouhozaman
Shabani, Robabeh
Eivazzadeh, Nazila
author_facet Faqihi, Fahime
Neshastehriz, Ali
Soleymanifard, Shokouhozaman
Shabani, Robabeh
Eivazzadeh, Nazila
author_sort Faqihi, Fahime
collection PubMed
description Radiation-induced bystander effects (RIBEs) are detected in cells that are not irradiated but receive signals from treated cells. The present study explored these bystander effects in a U87MG multicellular tumour spheroid model. A medium transfer technique was employed to induce the bystander effect, and colony formation assay was used to evaluate the effect. Relative changes in expression of BAX, BCL2, JNK and ERK genes were analysed using RT-PCR to investigate the RIBE mechanism. A significant decrease in plating efficiency was observed for both bystander and irradiated cells. The survival fraction was calculated for bystander cells to be 69.48% and for irradiated cells to be 34.68%. There was no change in pro-apoptotic BAX relative expression, but anti-apoptotic BCL2 showed downregulation in both irradiated and bystander cells. Pro-apoptotic JNK in bystander samples and ERK in irradiated samples were upregulated. The clonogenic survival data suggests that there was a classic RIBE in U87MG spheroids exposed to 4 Gy of X-rays, using a medium transfer technique. Changes in the expression of pro- and anti-apoptotic genes indicate involvement of both intrinsic apoptotic and MAPK pathways in inducing these effects.
format Online
Article
Text
id pubmed-4577008
institution National Center for Biotechnology Information
language English
publishDate 2015
publisher Oxford University Press
record_format MEDLINE/PubMed
spelling pubmed-45770082015-09-25 Radiation-induced bystander effect in non-irradiated glioblastoma spheroid cells Faqihi, Fahime Neshastehriz, Ali Soleymanifard, Shokouhozaman Shabani, Robabeh Eivazzadeh, Nazila J Radiat Res Biology Radiation-induced bystander effects (RIBEs) are detected in cells that are not irradiated but receive signals from treated cells. The present study explored these bystander effects in a U87MG multicellular tumour spheroid model. A medium transfer technique was employed to induce the bystander effect, and colony formation assay was used to evaluate the effect. Relative changes in expression of BAX, BCL2, JNK and ERK genes were analysed using RT-PCR to investigate the RIBE mechanism. A significant decrease in plating efficiency was observed for both bystander and irradiated cells. The survival fraction was calculated for bystander cells to be 69.48% and for irradiated cells to be 34.68%. There was no change in pro-apoptotic BAX relative expression, but anti-apoptotic BCL2 showed downregulation in both irradiated and bystander cells. Pro-apoptotic JNK in bystander samples and ERK in irradiated samples were upregulated. The clonogenic survival data suggests that there was a classic RIBE in U87MG spheroids exposed to 4 Gy of X-rays, using a medium transfer technique. Changes in the expression of pro- and anti-apoptotic genes indicate involvement of both intrinsic apoptotic and MAPK pathways in inducing these effects. Oxford University Press 2015-09 2015-07-09 /pmc/articles/PMC4577008/ /pubmed/26160180 http://dx.doi.org/10.1093/jrr/rrv039 Text en © The Author 2015. 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 Biology
Faqihi, Fahime
Neshastehriz, Ali
Soleymanifard, Shokouhozaman
Shabani, Robabeh
Eivazzadeh, Nazila
Radiation-induced bystander effect in non-irradiated glioblastoma spheroid cells
title Radiation-induced bystander effect in non-irradiated glioblastoma spheroid cells
title_full Radiation-induced bystander effect in non-irradiated glioblastoma spheroid cells
title_fullStr Radiation-induced bystander effect in non-irradiated glioblastoma spheroid cells
title_full_unstemmed Radiation-induced bystander effect in non-irradiated glioblastoma spheroid cells
title_short Radiation-induced bystander effect in non-irradiated glioblastoma spheroid cells
title_sort radiation-induced bystander effect in non-irradiated glioblastoma spheroid cells
topic Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4577008/
https://www.ncbi.nlm.nih.gov/pubmed/26160180
http://dx.doi.org/10.1093/jrr/rrv039
work_keys_str_mv AT faqihifahime radiationinducedbystandereffectinnonirradiatedglioblastomaspheroidcells
AT neshastehrizali radiationinducedbystandereffectinnonirradiatedglioblastomaspheroidcells
AT soleymanifardshokouhozaman radiationinducedbystandereffectinnonirradiatedglioblastomaspheroidcells
AT shabanirobabeh radiationinducedbystandereffectinnonirradiatedglioblastomaspheroidcells
AT eivazzadehnazila radiationinducedbystandereffectinnonirradiatedglioblastomaspheroidcells