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Mechanisms of Radiation Toxicity in Transformed and Non-Transformed Cells

Radiation damage to biological systems is determined by the type of radiation, the total dosage of exposure, the dose rate, and the region of the body exposed. Three modes of cell death—necrosis, apoptosis, and autophagy—as well as accelerated senescence have been demonstrated to occur in vitro and...

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Autores principales: Panganiban, Ronald-Allan M., Snow, Andrew L., Day, Regina M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Molecular Diversity Preservation International (MDPI) 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3759894/
https://www.ncbi.nlm.nih.gov/pubmed/23912235
http://dx.doi.org/10.3390/ijms140815931
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author Panganiban, Ronald-Allan M.
Snow, Andrew L.
Day, Regina M.
author_facet Panganiban, Ronald-Allan M.
Snow, Andrew L.
Day, Regina M.
author_sort Panganiban, Ronald-Allan M.
collection PubMed
description Radiation damage to biological systems is determined by the type of radiation, the total dosage of exposure, the dose rate, and the region of the body exposed. Three modes of cell death—necrosis, apoptosis, and autophagy—as well as accelerated senescence have been demonstrated to occur in vitro and in vivo in response to radiation in cancer cells as well as in normal cells. The basis for cellular selection for each mode depends on various factors including the specific cell type involved, the dose of radiation absorbed by the cell, and whether it is proliferating and/or transformed. Here we review the signaling mechanisms activated by radiation for the induction of toxicity in transformed and normal cells. Understanding the molecular mechanisms of radiation toxicity is critical for the development of radiation countermeasures as well as for the improvement of clinical radiation in cancer treatment.
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spelling pubmed-37598942013-09-03 Mechanisms of Radiation Toxicity in Transformed and Non-Transformed Cells Panganiban, Ronald-Allan M. Snow, Andrew L. Day, Regina M. Int J Mol Sci Review Radiation damage to biological systems is determined by the type of radiation, the total dosage of exposure, the dose rate, and the region of the body exposed. Three modes of cell death—necrosis, apoptosis, and autophagy—as well as accelerated senescence have been demonstrated to occur in vitro and in vivo in response to radiation in cancer cells as well as in normal cells. The basis for cellular selection for each mode depends on various factors including the specific cell type involved, the dose of radiation absorbed by the cell, and whether it is proliferating and/or transformed. Here we review the signaling mechanisms activated by radiation for the induction of toxicity in transformed and normal cells. Understanding the molecular mechanisms of radiation toxicity is critical for the development of radiation countermeasures as well as for the improvement of clinical radiation in cancer treatment. Molecular Diversity Preservation International (MDPI) 2013-07-31 /pmc/articles/PMC3759894/ /pubmed/23912235 http://dx.doi.org/10.3390/ijms140815931 Text en © 2013 by the authors; licensee MDPI, Basel, Switzerland http://creativecommons.org/licenses/by/3.0 This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/3.0/).
spellingShingle Review
Panganiban, Ronald-Allan M.
Snow, Andrew L.
Day, Regina M.
Mechanisms of Radiation Toxicity in Transformed and Non-Transformed Cells
title Mechanisms of Radiation Toxicity in Transformed and Non-Transformed Cells
title_full Mechanisms of Radiation Toxicity in Transformed and Non-Transformed Cells
title_fullStr Mechanisms of Radiation Toxicity in Transformed and Non-Transformed Cells
title_full_unstemmed Mechanisms of Radiation Toxicity in Transformed and Non-Transformed Cells
title_short Mechanisms of Radiation Toxicity in Transformed and Non-Transformed Cells
title_sort mechanisms of radiation toxicity in transformed and non-transformed cells
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3759894/
https://www.ncbi.nlm.nih.gov/pubmed/23912235
http://dx.doi.org/10.3390/ijms140815931
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