author_facet Zhao, Weiling
Chuang, Eric Y.
Mishra, Mark
Awwad, Rania
Bisht, Kheem
Sun, Lunching
Nguyen, Phuongmai
Pennington, J. Daniel
Wang, Tony Jau Cheng
Bradbury, C. Matthew
Huang, Lei
Chen, Zhijun
Bar-Sela, Gil
Robbins, Michael E.C.
Gius, David
Zhao, Weiling
Chuang, Eric Y.
Mishra, Mark
Awwad, Rania
Bisht, Kheem
Sun, Lunching
Nguyen, Phuongmai
Pennington, J. Daniel
Wang, Tony Jau Cheng
Bradbury, C. Matthew
Huang, Lei
Chen, Zhijun
Bar-Sela, Gil
Robbins, Michael E.C.
Gius, David
author Zhao, Weiling
Chuang, Eric Y.
Mishra, Mark
Awwad, Rania
Bisht, Kheem
Sun, Lunching
Nguyen, Phuongmai
Pennington, J. Daniel
Wang, Tony Jau Cheng
Bradbury, C. Matthew
Huang, Lei
Chen, Zhijun
Bar-Sela, Gil
Robbins, Michael E.C.
Gius, David
spellingShingle Zhao, Weiling
Chuang, Eric Y.
Mishra, Mark
Awwad, Rania
Bisht, Kheem
Sun, Lunching
Nguyen, Phuongmai
Pennington, J. Daniel
Wang, Tony Jau Cheng
Bradbury, C. Matthew
Huang, Lei
Chen, Zhijun
Bar-Sela, Gil
Robbins, Michael E.C.
Gius, David
Clinical Cancer Research
Distinct Effects of Ionizing Radiation on In vivo Murine Kidney and Brain Normal Tissue Gene Expression
Cancer Research
Oncology
author_sort zhao, weiling
spelling Zhao, Weiling Chuang, Eric Y. Mishra, Mark Awwad, Rania Bisht, Kheem Sun, Lunching Nguyen, Phuongmai Pennington, J. Daniel Wang, Tony Jau Cheng Bradbury, C. Matthew Huang, Lei Chen, Zhijun Bar-Sela, Gil Robbins, Michael E.C. Gius, David 1078-0432 1557-3265 American Association for Cancer Research (AACR) Cancer Research Oncology http://dx.doi.org/10.1158/1078-0432.ccr-05-2418 <jats:title>Abstract</jats:title> <jats:p>Purpose: There is a growing awareness that radiation-induced normal tissue injury in late-responding organs, such as the brain, kidney, and lung, involves complex and dynamic responses between multiple cell types that not only lead to targeted cell death but also acute and chronic alterations in cell function. The specific genes involved in the acute and chronic responses of these late-responding normal tissues remain ill defined; understanding these changes is critical to understanding the mechanism of organ damage. As such, the aim of the present study was to identify candidate genes involved in the development of radiation injury in the murine kidney and brain using microarray analysis.</jats:p> <jats:p>Experimental Design: A multimodality experimental approach combined with a comprehensive expression analysis was done to determine changes in normal murine tissue gene expression at 8 and 24 hours after irradiation.</jats:p> <jats:p>Results: A comparison of the gene expression patterns in normal mouse kidney and brain was strikingly different. This observation was surprising because it has been long assumed that the changes in irradiation-induced gene expression in normal tissues are preprogrammed genetic changes that are not affected by tissue-specific origin.</jats:p> <jats:p>Conclusions: This study shows the potential of microarray analysis to identify gene expression changes in irradiated normal tissue cells and suggests how normal cells respond to the damaging effects of ionizing radiation is complex and markedly different in cells of differing origin.</jats:p> Distinct Effects of Ionizing Radiation on <i>In vivo</i> Murine Kidney and Brain Normal Tissue Gene Expression Clinical Cancer Research
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title Distinct Effects of Ionizing Radiation on In vivo Murine Kidney and Brain Normal Tissue Gene Expression
title_unstemmed Distinct Effects of Ionizing Radiation on In vivo Murine Kidney and Brain Normal Tissue Gene Expression
title_full Distinct Effects of Ionizing Radiation on In vivo Murine Kidney and Brain Normal Tissue Gene Expression
title_fullStr Distinct Effects of Ionizing Radiation on In vivo Murine Kidney and Brain Normal Tissue Gene Expression
title_full_unstemmed Distinct Effects of Ionizing Radiation on In vivo Murine Kidney and Brain Normal Tissue Gene Expression
title_short Distinct Effects of Ionizing Radiation on In vivo Murine Kidney and Brain Normal Tissue Gene Expression
title_sort distinct effects of ionizing radiation on <i>in vivo</i> murine kidney and brain normal tissue gene expression
topic Cancer Research
Oncology
url http://dx.doi.org/10.1158/1078-0432.ccr-05-2418
publishDate 2006
physical 3823-3830
description <jats:title>Abstract</jats:title> <jats:p>Purpose: There is a growing awareness that radiation-induced normal tissue injury in late-responding organs, such as the brain, kidney, and lung, involves complex and dynamic responses between multiple cell types that not only lead to targeted cell death but also acute and chronic alterations in cell function. The specific genes involved in the acute and chronic responses of these late-responding normal tissues remain ill defined; understanding these changes is critical to understanding the mechanism of organ damage. As such, the aim of the present study was to identify candidate genes involved in the development of radiation injury in the murine kidney and brain using microarray analysis.</jats:p> <jats:p>Experimental Design: A multimodality experimental approach combined with a comprehensive expression analysis was done to determine changes in normal murine tissue gene expression at 8 and 24 hours after irradiation.</jats:p> <jats:p>Results: A comparison of the gene expression patterns in normal mouse kidney and brain was strikingly different. This observation was surprising because it has been long assumed that the changes in irradiation-induced gene expression in normal tissues are preprogrammed genetic changes that are not affected by tissue-specific origin.</jats:p> <jats:p>Conclusions: This study shows the potential of microarray analysis to identify gene expression changes in irradiated normal tissue cells and suggests how normal cells respond to the damaging effects of ionizing radiation is complex and markedly different in cells of differing origin.</jats:p>
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author Zhao, Weiling, Chuang, Eric Y., Mishra, Mark, Awwad, Rania, Bisht, Kheem, Sun, Lunching, Nguyen, Phuongmai, Pennington, J. Daniel, Wang, Tony Jau Cheng, Bradbury, C. Matthew, Huang, Lei, Chen, Zhijun, Bar-Sela, Gil, Robbins, Michael E.C., Gius, David
author_facet Zhao, Weiling, Chuang, Eric Y., Mishra, Mark, Awwad, Rania, Bisht, Kheem, Sun, Lunching, Nguyen, Phuongmai, Pennington, J. Daniel, Wang, Tony Jau Cheng, Bradbury, C. Matthew, Huang, Lei, Chen, Zhijun, Bar-Sela, Gil, Robbins, Michael E.C., Gius, David, Zhao, Weiling, Chuang, Eric Y., Mishra, Mark, Awwad, Rania, Bisht, Kheem, Sun, Lunching, Nguyen, Phuongmai, Pennington, J. Daniel, Wang, Tony Jau Cheng, Bradbury, C. Matthew, Huang, Lei, Chen, Zhijun, Bar-Sela, Gil, Robbins, Michael E.C., Gius, David
author_sort zhao, weiling
container_issue 12
container_start_page 3823
container_title Clinical Cancer Research
container_volume 12
description <jats:title>Abstract</jats:title> <jats:p>Purpose: There is a growing awareness that radiation-induced normal tissue injury in late-responding organs, such as the brain, kidney, and lung, involves complex and dynamic responses between multiple cell types that not only lead to targeted cell death but also acute and chronic alterations in cell function. The specific genes involved in the acute and chronic responses of these late-responding normal tissues remain ill defined; understanding these changes is critical to understanding the mechanism of organ damage. As such, the aim of the present study was to identify candidate genes involved in the development of radiation injury in the murine kidney and brain using microarray analysis.</jats:p> <jats:p>Experimental Design: A multimodality experimental approach combined with a comprehensive expression analysis was done to determine changes in normal murine tissue gene expression at 8 and 24 hours after irradiation.</jats:p> <jats:p>Results: A comparison of the gene expression patterns in normal mouse kidney and brain was strikingly different. This observation was surprising because it has been long assumed that the changes in irradiation-induced gene expression in normal tissues are preprogrammed genetic changes that are not affected by tissue-specific origin.</jats:p> <jats:p>Conclusions: This study shows the potential of microarray analysis to identify gene expression changes in irradiated normal tissue cells and suggests how normal cells respond to the damaging effects of ionizing radiation is complex and markedly different in cells of differing origin.</jats:p>
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spelling Zhao, Weiling Chuang, Eric Y. Mishra, Mark Awwad, Rania Bisht, Kheem Sun, Lunching Nguyen, Phuongmai Pennington, J. Daniel Wang, Tony Jau Cheng Bradbury, C. Matthew Huang, Lei Chen, Zhijun Bar-Sela, Gil Robbins, Michael E.C. Gius, David 1078-0432 1557-3265 American Association for Cancer Research (AACR) Cancer Research Oncology http://dx.doi.org/10.1158/1078-0432.ccr-05-2418 <jats:title>Abstract</jats:title> <jats:p>Purpose: There is a growing awareness that radiation-induced normal tissue injury in late-responding organs, such as the brain, kidney, and lung, involves complex and dynamic responses between multiple cell types that not only lead to targeted cell death but also acute and chronic alterations in cell function. The specific genes involved in the acute and chronic responses of these late-responding normal tissues remain ill defined; understanding these changes is critical to understanding the mechanism of organ damage. As such, the aim of the present study was to identify candidate genes involved in the development of radiation injury in the murine kidney and brain using microarray analysis.</jats:p> <jats:p>Experimental Design: A multimodality experimental approach combined with a comprehensive expression analysis was done to determine changes in normal murine tissue gene expression at 8 and 24 hours after irradiation.</jats:p> <jats:p>Results: A comparison of the gene expression patterns in normal mouse kidney and brain was strikingly different. This observation was surprising because it has been long assumed that the changes in irradiation-induced gene expression in normal tissues are preprogrammed genetic changes that are not affected by tissue-specific origin.</jats:p> <jats:p>Conclusions: This study shows the potential of microarray analysis to identify gene expression changes in irradiated normal tissue cells and suggests how normal cells respond to the damaging effects of ionizing radiation is complex and markedly different in cells of differing origin.</jats:p> Distinct Effects of Ionizing Radiation on <i>In vivo</i> Murine Kidney and Brain Normal Tissue Gene Expression Clinical Cancer Research
spellingShingle Zhao, Weiling, Chuang, Eric Y., Mishra, Mark, Awwad, Rania, Bisht, Kheem, Sun, Lunching, Nguyen, Phuongmai, Pennington, J. Daniel, Wang, Tony Jau Cheng, Bradbury, C. Matthew, Huang, Lei, Chen, Zhijun, Bar-Sela, Gil, Robbins, Michael E.C., Gius, David, Clinical Cancer Research, Distinct Effects of Ionizing Radiation on In vivo Murine Kidney and Brain Normal Tissue Gene Expression, Cancer Research, Oncology
title Distinct Effects of Ionizing Radiation on In vivo Murine Kidney and Brain Normal Tissue Gene Expression
title_full Distinct Effects of Ionizing Radiation on In vivo Murine Kidney and Brain Normal Tissue Gene Expression
title_fullStr Distinct Effects of Ionizing Radiation on In vivo Murine Kidney and Brain Normal Tissue Gene Expression
title_full_unstemmed Distinct Effects of Ionizing Radiation on In vivo Murine Kidney and Brain Normal Tissue Gene Expression
title_short Distinct Effects of Ionizing Radiation on In vivo Murine Kidney and Brain Normal Tissue Gene Expression
title_sort distinct effects of ionizing radiation on <i>in vivo</i> murine kidney and brain normal tissue gene expression
title_unstemmed Distinct Effects of Ionizing Radiation on In vivo Murine Kidney and Brain Normal Tissue Gene Expression
topic Cancer Research, Oncology
url http://dx.doi.org/10.1158/1078-0432.ccr-05-2418