Portrait of inflammatory response to ionizing radiation treatment
Abstract Ionizing radiation (IR) activates both pro-and anti-proliferative signal pathways producing an imbalance in cell fate decision. IR is able to regulate several genes and factors involved in cell-cycle progression, survival and/or cell death, DNA repair and inflammation modulating an intracel...
Ausführliche Beschreibung
Autor*in: |
Di Maggio, Federica Maria [verfasserIn] |
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E-Artikel |
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Sprache: |
Englisch |
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2015 |
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Anmerkung: |
© Di Maggio et al.; licensee BioMed Central. 2015. This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( |
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Übergeordnetes Werk: |
Enthalten in: Journal of Inflammation - London : BioMed Central, 2004, 12(2015), 1 vom: 18. Feb. |
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Übergeordnetes Werk: |
volume:12 ; year:2015 ; number:1 ; day:18 ; month:02 |
Links: |
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DOI / URN: |
10.1186/s12950-015-0058-3 |
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520 | |a Abstract Ionizing radiation (IR) activates both pro-and anti-proliferative signal pathways producing an imbalance in cell fate decision. IR is able to regulate several genes and factors involved in cell-cycle progression, survival and/or cell death, DNA repair and inflammation modulating an intracellular radiation-dependent response. Radiation therapy can modulate anti-tumour immune responses, modifying tumour and its microenvironment. In this review, we report how IR could stimulate inflammatory factors to affect cell fate via multiple pathways, describing their roles on gene expression regulation, fibrosis and invasive processes. Understanding the complex relationship between IR, inflammation and immune responses in cancer, opens up new avenues for radiation research and therapy in order to optimize and personalize radiation therapy treatment for each patient. | ||
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700 | 1 | |a Messa, Cristina |4 aut | |
700 | 1 | |a Gilardi, Maria Carla |4 aut | |
700 | 1 | |a Bravatà, Valentina |4 aut | |
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10.1186/s12950-015-0058-3 doi (DE-627)SPR029451337 (SPR)s12950-015-0058-3-e DE-627 ger DE-627 rakwb eng Di Maggio, Federica Maria verfasserin aut Portrait of inflammatory response to ionizing radiation treatment 2015 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © Di Maggio et al.; licensee BioMed Central. 2015. This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( Abstract Ionizing radiation (IR) activates both pro-and anti-proliferative signal pathways producing an imbalance in cell fate decision. IR is able to regulate several genes and factors involved in cell-cycle progression, survival and/or cell death, DNA repair and inflammation modulating an intracellular radiation-dependent response. Radiation therapy can modulate anti-tumour immune responses, modifying tumour and its microenvironment. In this review, we report how IR could stimulate inflammatory factors to affect cell fate via multiple pathways, describing their roles on gene expression regulation, fibrosis and invasive processes. Understanding the complex relationship between IR, inflammation and immune responses in cancer, opens up new avenues for radiation research and therapy in order to optimize and personalize radiation therapy treatment for each patient. Ionizing radiation (dpeaa)DE-He213 Inflammation (dpeaa)DE-He213 Cytokine (dpeaa)DE-He213 Fibrosis (dpeaa)DE-He213 Invasiveness (dpeaa)DE-He213 Minafra, Luigi aut Forte, Giusi Irma aut Cammarata, Francesco Paolo aut Lio, Domenico aut Messa, Cristina aut Gilardi, Maria Carla aut Bravatà, Valentina aut Enthalten in Journal of Inflammation London : BioMed Central, 2004 12(2015), 1 vom: 18. Feb. (DE-627)461908018 (DE-600)2164385-4 1476-9255 nnns volume:12 year:2015 number:1 day:18 month:02 https://dx.doi.org/10.1186/s12950-015-0058-3 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_73 GBV_ILN_74 GBV_ILN_95 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_206 GBV_ILN_213 GBV_ILN_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_602 GBV_ILN_2003 GBV_ILN_2014 GBV_ILN_4012 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4249 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4700 AR 12 2015 1 18 02 |
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10.1186/s12950-015-0058-3 doi (DE-627)SPR029451337 (SPR)s12950-015-0058-3-e DE-627 ger DE-627 rakwb eng Di Maggio, Federica Maria verfasserin aut Portrait of inflammatory response to ionizing radiation treatment 2015 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © Di Maggio et al.; licensee BioMed Central. 2015. This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( Abstract Ionizing radiation (IR) activates both pro-and anti-proliferative signal pathways producing an imbalance in cell fate decision. IR is able to regulate several genes and factors involved in cell-cycle progression, survival and/or cell death, DNA repair and inflammation modulating an intracellular radiation-dependent response. Radiation therapy can modulate anti-tumour immune responses, modifying tumour and its microenvironment. In this review, we report how IR could stimulate inflammatory factors to affect cell fate via multiple pathways, describing their roles on gene expression regulation, fibrosis and invasive processes. Understanding the complex relationship between IR, inflammation and immune responses in cancer, opens up new avenues for radiation research and therapy in order to optimize and personalize radiation therapy treatment for each patient. Ionizing radiation (dpeaa)DE-He213 Inflammation (dpeaa)DE-He213 Cytokine (dpeaa)DE-He213 Fibrosis (dpeaa)DE-He213 Invasiveness (dpeaa)DE-He213 Minafra, Luigi aut Forte, Giusi Irma aut Cammarata, Francesco Paolo aut Lio, Domenico aut Messa, Cristina aut Gilardi, Maria Carla aut Bravatà, Valentina aut Enthalten in Journal of Inflammation London : BioMed Central, 2004 12(2015), 1 vom: 18. Feb. (DE-627)461908018 (DE-600)2164385-4 1476-9255 nnns volume:12 year:2015 number:1 day:18 month:02 https://dx.doi.org/10.1186/s12950-015-0058-3 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_73 GBV_ILN_74 GBV_ILN_95 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_206 GBV_ILN_213 GBV_ILN_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_602 GBV_ILN_2003 GBV_ILN_2014 GBV_ILN_4012 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4249 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4700 AR 12 2015 1 18 02 |
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10.1186/s12950-015-0058-3 doi (DE-627)SPR029451337 (SPR)s12950-015-0058-3-e DE-627 ger DE-627 rakwb eng Di Maggio, Federica Maria verfasserin aut Portrait of inflammatory response to ionizing radiation treatment 2015 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © Di Maggio et al.; licensee BioMed Central. 2015. This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( Abstract Ionizing radiation (IR) activates both pro-and anti-proliferative signal pathways producing an imbalance in cell fate decision. IR is able to regulate several genes and factors involved in cell-cycle progression, survival and/or cell death, DNA repair and inflammation modulating an intracellular radiation-dependent response. Radiation therapy can modulate anti-tumour immune responses, modifying tumour and its microenvironment. In this review, we report how IR could stimulate inflammatory factors to affect cell fate via multiple pathways, describing their roles on gene expression regulation, fibrosis and invasive processes. Understanding the complex relationship between IR, inflammation and immune responses in cancer, opens up new avenues for radiation research and therapy in order to optimize and personalize radiation therapy treatment for each patient. Ionizing radiation (dpeaa)DE-He213 Inflammation (dpeaa)DE-He213 Cytokine (dpeaa)DE-He213 Fibrosis (dpeaa)DE-He213 Invasiveness (dpeaa)DE-He213 Minafra, Luigi aut Forte, Giusi Irma aut Cammarata, Francesco Paolo aut Lio, Domenico aut Messa, Cristina aut Gilardi, Maria Carla aut Bravatà, Valentina aut Enthalten in Journal of Inflammation London : BioMed Central, 2004 12(2015), 1 vom: 18. Feb. (DE-627)461908018 (DE-600)2164385-4 1476-9255 nnns volume:12 year:2015 number:1 day:18 month:02 https://dx.doi.org/10.1186/s12950-015-0058-3 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_73 GBV_ILN_74 GBV_ILN_95 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_206 GBV_ILN_213 GBV_ILN_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_602 GBV_ILN_2003 GBV_ILN_2014 GBV_ILN_4012 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4249 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4700 AR 12 2015 1 18 02 |
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10.1186/s12950-015-0058-3 doi (DE-627)SPR029451337 (SPR)s12950-015-0058-3-e DE-627 ger DE-627 rakwb eng Di Maggio, Federica Maria verfasserin aut Portrait of inflammatory response to ionizing radiation treatment 2015 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © Di Maggio et al.; licensee BioMed Central. 2015. This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( Abstract Ionizing radiation (IR) activates both pro-and anti-proliferative signal pathways producing an imbalance in cell fate decision. IR is able to regulate several genes and factors involved in cell-cycle progression, survival and/or cell death, DNA repair and inflammation modulating an intracellular radiation-dependent response. Radiation therapy can modulate anti-tumour immune responses, modifying tumour and its microenvironment. In this review, we report how IR could stimulate inflammatory factors to affect cell fate via multiple pathways, describing their roles on gene expression regulation, fibrosis and invasive processes. Understanding the complex relationship between IR, inflammation and immune responses in cancer, opens up new avenues for radiation research and therapy in order to optimize and personalize radiation therapy treatment for each patient. Ionizing radiation (dpeaa)DE-He213 Inflammation (dpeaa)DE-He213 Cytokine (dpeaa)DE-He213 Fibrosis (dpeaa)DE-He213 Invasiveness (dpeaa)DE-He213 Minafra, Luigi aut Forte, Giusi Irma aut Cammarata, Francesco Paolo aut Lio, Domenico aut Messa, Cristina aut Gilardi, Maria Carla aut Bravatà, Valentina aut Enthalten in Journal of Inflammation London : BioMed Central, 2004 12(2015), 1 vom: 18. Feb. (DE-627)461908018 (DE-600)2164385-4 1476-9255 nnns volume:12 year:2015 number:1 day:18 month:02 https://dx.doi.org/10.1186/s12950-015-0058-3 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_73 GBV_ILN_74 GBV_ILN_95 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_206 GBV_ILN_213 GBV_ILN_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_602 GBV_ILN_2003 GBV_ILN_2014 GBV_ILN_4012 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4249 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4700 AR 12 2015 1 18 02 |
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10.1186/s12950-015-0058-3 doi (DE-627)SPR029451337 (SPR)s12950-015-0058-3-e DE-627 ger DE-627 rakwb eng Di Maggio, Federica Maria verfasserin aut Portrait of inflammatory response to ionizing radiation treatment 2015 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © Di Maggio et al.; licensee BioMed Central. 2015. This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( Abstract Ionizing radiation (IR) activates both pro-and anti-proliferative signal pathways producing an imbalance in cell fate decision. IR is able to regulate several genes and factors involved in cell-cycle progression, survival and/or cell death, DNA repair and inflammation modulating an intracellular radiation-dependent response. Radiation therapy can modulate anti-tumour immune responses, modifying tumour and its microenvironment. In this review, we report how IR could stimulate inflammatory factors to affect cell fate via multiple pathways, describing their roles on gene expression regulation, fibrosis and invasive processes. Understanding the complex relationship between IR, inflammation and immune responses in cancer, opens up new avenues for radiation research and therapy in order to optimize and personalize radiation therapy treatment for each patient. Ionizing radiation (dpeaa)DE-He213 Inflammation (dpeaa)DE-He213 Cytokine (dpeaa)DE-He213 Fibrosis (dpeaa)DE-He213 Invasiveness (dpeaa)DE-He213 Minafra, Luigi aut Forte, Giusi Irma aut Cammarata, Francesco Paolo aut Lio, Domenico aut Messa, Cristina aut Gilardi, Maria Carla aut Bravatà, Valentina aut Enthalten in Journal of Inflammation London : BioMed Central, 2004 12(2015), 1 vom: 18. Feb. (DE-627)461908018 (DE-600)2164385-4 1476-9255 nnns volume:12 year:2015 number:1 day:18 month:02 https://dx.doi.org/10.1186/s12950-015-0058-3 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_73 GBV_ILN_74 GBV_ILN_95 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_206 GBV_ILN_213 GBV_ILN_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_602 GBV_ILN_2003 GBV_ILN_2014 GBV_ILN_4012 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4249 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4700 AR 12 2015 1 18 02 |
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Abstract Ionizing radiation (IR) activates both pro-and anti-proliferative signal pathways producing an imbalance in cell fate decision. IR is able to regulate several genes and factors involved in cell-cycle progression, survival and/or cell death, DNA repair and inflammation modulating an intracellular radiation-dependent response. Radiation therapy can modulate anti-tumour immune responses, modifying tumour and its microenvironment. In this review, we report how IR could stimulate inflammatory factors to affect cell fate via multiple pathways, describing their roles on gene expression regulation, fibrosis and invasive processes. Understanding the complex relationship between IR, inflammation and immune responses in cancer, opens up new avenues for radiation research and therapy in order to optimize and personalize radiation therapy treatment for each patient. © Di Maggio et al.; licensee BioMed Central. 2015. This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( |
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Abstract Ionizing radiation (IR) activates both pro-and anti-proliferative signal pathways producing an imbalance in cell fate decision. IR is able to regulate several genes and factors involved in cell-cycle progression, survival and/or cell death, DNA repair and inflammation modulating an intracellular radiation-dependent response. Radiation therapy can modulate anti-tumour immune responses, modifying tumour and its microenvironment. In this review, we report how IR could stimulate inflammatory factors to affect cell fate via multiple pathways, describing their roles on gene expression regulation, fibrosis and invasive processes. Understanding the complex relationship between IR, inflammation and immune responses in cancer, opens up new avenues for radiation research and therapy in order to optimize and personalize radiation therapy treatment for each patient. © Di Maggio et al.; licensee BioMed Central. 2015. This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( |
abstract_unstemmed |
Abstract Ionizing radiation (IR) activates both pro-and anti-proliferative signal pathways producing an imbalance in cell fate decision. IR is able to regulate several genes and factors involved in cell-cycle progression, survival and/or cell death, DNA repair and inflammation modulating an intracellular radiation-dependent response. Radiation therapy can modulate anti-tumour immune responses, modifying tumour and its microenvironment. In this review, we report how IR could stimulate inflammatory factors to affect cell fate via multiple pathways, describing their roles on gene expression regulation, fibrosis and invasive processes. Understanding the complex relationship between IR, inflammation and immune responses in cancer, opens up new avenues for radiation research and therapy in order to optimize and personalize radiation therapy treatment for each patient. © Di Maggio et al.; licensee BioMed Central. 2015. This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( |
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score |
7.402793 |