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Effect of radiation on brain tissue endothelin-1 level and tumor development
BACKGROUND: Radiotherapy causes injury in the endothelial cells of blood vessels and the production of vasoactive amines such as endothelin-1 (ET-1). ET-1 is an important peptide in cancer development. In this study, the effects of radiation on brain tissue ET-1 level were evaluated. Is it possible...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Medknow Publications & Media Pvt Ltd
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5409363/ https://www.ncbi.nlm.nih.gov/pubmed/28484527 http://dx.doi.org/10.4103/1793-5482.145575 |
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author | Kaplan, Metin Kılınç, Ahmet Ozturk, Sait Ilhan, Nevin Gurocak, Simay Gonen, Murat |
author_facet | Kaplan, Metin Kılınç, Ahmet Ozturk, Sait Ilhan, Nevin Gurocak, Simay Gonen, Murat |
author_sort | Kaplan, Metin |
collection | PubMed |
description | BACKGROUND: Radiotherapy causes injury in the endothelial cells of blood vessels and the production of vasoactive amines such as endothelin-1 (ET-1). ET-1 is an important peptide in cancer development. In this study, the effects of radiation on brain tissue ET-1 level were evaluated. Is it possible to suggest a mechanism using ET-1 level in the production of this adverse effect? In this paper, the relationship between the development of brain tumors and the ET-1 level has been discussed. MATERIALS AND METHODS: Twenty-eight adult Sprague Dawley rats were used in the experiments. The rats were divided into four groups (n = 7) as follows: control group: radiation was not applied during the experiment; Group 1: Decapitated on the 1(st) day following radiation; Group 2: Decapitated on the 7(th) day following radiation; and Group 3: Decapitated on the 30(th) day following radiation. ET-1 levels were measured with enzyme-linked immunosorbent assay (ELISA) method. The t-test, variance analysis, and Tukey honestly significant difference (HSD) tests were used in the statistical analysis. A value of P < 0.05 was accepted as significant. RESULTS: No statistical differences were observed in the tissue ET-1 levels between the control group and other groups. According to the variance analysis and Tukey test, the differences between the groups were not significant. CONCLUSION: We observed in this study that the effects of radiation on brain tumor development or malignant transformation are not mediated by ET-1 levels. In addition, these results support the hypothesis of the fact that medical treatment with ET-1 antagonists in clinical cases receiving radiotheraphy is unnecessary. |
format | Online Article Text |
id | pubmed-5409363 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Medknow Publications & Media Pvt Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-54093632017-05-08 Effect of radiation on brain tissue endothelin-1 level and tumor development Kaplan, Metin Kılınç, Ahmet Ozturk, Sait Ilhan, Nevin Gurocak, Simay Gonen, Murat Asian J Neurosurg Original Article BACKGROUND: Radiotherapy causes injury in the endothelial cells of blood vessels and the production of vasoactive amines such as endothelin-1 (ET-1). ET-1 is an important peptide in cancer development. In this study, the effects of radiation on brain tissue ET-1 level were evaluated. Is it possible to suggest a mechanism using ET-1 level in the production of this adverse effect? In this paper, the relationship between the development of brain tumors and the ET-1 level has been discussed. MATERIALS AND METHODS: Twenty-eight adult Sprague Dawley rats were used in the experiments. The rats were divided into four groups (n = 7) as follows: control group: radiation was not applied during the experiment; Group 1: Decapitated on the 1(st) day following radiation; Group 2: Decapitated on the 7(th) day following radiation; and Group 3: Decapitated on the 30(th) day following radiation. ET-1 levels were measured with enzyme-linked immunosorbent assay (ELISA) method. The t-test, variance analysis, and Tukey honestly significant difference (HSD) tests were used in the statistical analysis. A value of P < 0.05 was accepted as significant. RESULTS: No statistical differences were observed in the tissue ET-1 levels between the control group and other groups. According to the variance analysis and Tukey test, the differences between the groups were not significant. CONCLUSION: We observed in this study that the effects of radiation on brain tumor development or malignant transformation are not mediated by ET-1 levels. In addition, these results support the hypothesis of the fact that medical treatment with ET-1 antagonists in clinical cases receiving radiotheraphy is unnecessary. Medknow Publications & Media Pvt Ltd 2017 /pmc/articles/PMC5409363/ /pubmed/28484527 http://dx.doi.org/10.4103/1793-5482.145575 Text en Copyright: © 2014 Asian Journal of Neurosurgery http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 3.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as the author is credited and the new creations are licensed under the identical terms. |
spellingShingle | Original Article Kaplan, Metin Kılınç, Ahmet Ozturk, Sait Ilhan, Nevin Gurocak, Simay Gonen, Murat Effect of radiation on brain tissue endothelin-1 level and tumor development |
title | Effect of radiation on brain tissue endothelin-1 level and tumor development |
title_full | Effect of radiation on brain tissue endothelin-1 level and tumor development |
title_fullStr | Effect of radiation on brain tissue endothelin-1 level and tumor development |
title_full_unstemmed | Effect of radiation on brain tissue endothelin-1 level and tumor development |
title_short | Effect of radiation on brain tissue endothelin-1 level and tumor development |
title_sort | effect of radiation on brain tissue endothelin-1 level and tumor development |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5409363/ https://www.ncbi.nlm.nih.gov/pubmed/28484527 http://dx.doi.org/10.4103/1793-5482.145575 |
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