Implications of Hyperoxia over the Tumor Microenvironment: An Overview Highlighting the Importance of the Immune System

Hyperoxia is used in order to counteract hypoxia effects in the TME (tumor microenvironment), which are described to boost the malignant tumor phenotype and poor prognosis. The reduction of tumor hypoxic state through the formation of a non-aberrant vasculature or an increase in the toxicity of the...
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Autor*in:	Ana Belén Herrera-Campos [verfasserIn] Esteban Zamudio-Martinez [verfasserIn] Daniel Delgado-Bellido [verfasserIn] Mónica Fernández-Cortés [verfasserIn] Luis M. Montuenga [verfasserIn] F. Javier Oliver [verfasserIn] Angel Garcia-Diaz [verfasserIn]

Format:	E-Artikel
Sprache:	Englisch

Erschienen:	2022

Schlagwörter:	tumor microenvironment hypoxia hyperoxia immunotherapy inflammation

Übergeordnetes Werk:	In: Cancers - MDPI AG, 2010, 14(2022), 11, p 2740
Übergeordnetes Werk:	volume:14 ; year:2022 ; number:11, p 2740

Links:	Link aufrufen Link aufrufen Link aufrufen Journal toc

DOI / URN:	10.3390/cancers14112740

Katalog-ID:	DOAJ022410759

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allfields	10.3390/cancers14112740 doi (DE-627)DOAJ022410759 (DE-599)DOAJ2698dba378ab4534840ad8411061bc53 DE-627 ger DE-627 rakwb eng RC254-282 Ana Belén Herrera-Campos verfasserin aut Implications of Hyperoxia over the Tumor Microenvironment: An Overview Highlighting the Importance of the Immune System 2022 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Hyperoxia is used in order to counteract hypoxia effects in the TME (tumor microenvironment), which are described to boost the malignant tumor phenotype and poor prognosis. The reduction of tumor hypoxic state through the formation of a non-aberrant vasculature or an increase in the toxicity of the therapeutic agent improves the efficacy of therapies such as chemotherapy. Radiotherapy efficacy has also improved, where apoptotic mechanisms seem to be implicated. Moreover, hyperoxia increases the antitumor immunity through diverse pathways, leading to an immunopermissive TME. Although hyperoxia is an approved treatment for preventing and treating hypoxemia, it has harmful side-effects. Prolonged exposure to high oxygen levels may cause acute lung injury, characterized by an exacerbated immune response, and the destruction of the alveolar–capillary barrier. Furthermore, under this situation, the high concentration of ROS may cause toxicity that will lead not only to cell death but also to an increase in chemoattractant and proinflammatory cytokine secretion. This would end in a lung leukocyte recruitment and, therefore, lung damage. Moreover, unregulated inflammation causes different consequences promoting tumor development and metastasis. This process is known as protumor inflammation, where different cell types and molecules are implicated; for instance, IL-1β has been described as a key cytokine. Although current results show benefits over cancer therapies using hyperoxia, further studies need to be conducted, not only to improve tumor regression, but also to prevent its collateral damage. tumor microenvironment hypoxia hyperoxia immunotherapy inflammation Neoplasms. Tumors. Oncology. Including cancer and carcinogens Esteban Zamudio-Martinez verfasserin aut Daniel Delgado-Bellido verfasserin aut Mónica Fernández-Cortés verfasserin aut Luis M. Montuenga verfasserin aut F. Javier Oliver verfasserin aut Angel Garcia-Diaz verfasserin aut In Cancers MDPI AG, 2010 14(2022), 11, p 2740 (DE-627)614095670 (DE-600)2527080-1 20726694 nnns volume:14 year:2022 number:11, p 2740 https://doi.org/10.3390/cancers14112740 kostenfrei https://doaj.org/article/2698dba378ab4534840ad8411061bc53 kostenfrei https://www.mdpi.com/2072-6694/14/11/2740 kostenfrei https://doaj.org/toc/2072-6694 Journal toc kostenfrei GBV_USEFLAG_A SYSFLAG_A GBV_DOAJ 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_2005 GBV_ILN_2009 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2055 GBV_ILN_2111 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 14 2022 11, p 2740
spelling	10.3390/cancers14112740 doi (DE-627)DOAJ022410759 (DE-599)DOAJ2698dba378ab4534840ad8411061bc53 DE-627 ger DE-627 rakwb eng RC254-282 Ana Belén Herrera-Campos verfasserin aut Implications of Hyperoxia over the Tumor Microenvironment: An Overview Highlighting the Importance of the Immune System 2022 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Hyperoxia is used in order to counteract hypoxia effects in the TME (tumor microenvironment), which are described to boost the malignant tumor phenotype and poor prognosis. The reduction of tumor hypoxic state through the formation of a non-aberrant vasculature or an increase in the toxicity of the therapeutic agent improves the efficacy of therapies such as chemotherapy. Radiotherapy efficacy has also improved, where apoptotic mechanisms seem to be implicated. Moreover, hyperoxia increases the antitumor immunity through diverse pathways, leading to an immunopermissive TME. Although hyperoxia is an approved treatment for preventing and treating hypoxemia, it has harmful side-effects. Prolonged exposure to high oxygen levels may cause acute lung injury, characterized by an exacerbated immune response, and the destruction of the alveolar–capillary barrier. Furthermore, under this situation, the high concentration of ROS may cause toxicity that will lead not only to cell death but also to an increase in chemoattractant and proinflammatory cytokine secretion. This would end in a lung leukocyte recruitment and, therefore, lung damage. Moreover, unregulated inflammation causes different consequences promoting tumor development and metastasis. This process is known as protumor inflammation, where different cell types and molecules are implicated; for instance, IL-1β has been described as a key cytokine. Although current results show benefits over cancer therapies using hyperoxia, further studies need to be conducted, not only to improve tumor regression, but also to prevent its collateral damage. tumor microenvironment hypoxia hyperoxia immunotherapy inflammation Neoplasms. Tumors. Oncology. Including cancer and carcinogens Esteban Zamudio-Martinez verfasserin aut Daniel Delgado-Bellido verfasserin aut Mónica Fernández-Cortés verfasserin aut Luis M. Montuenga verfasserin aut F. Javier Oliver verfasserin aut Angel Garcia-Diaz verfasserin aut In Cancers MDPI AG, 2010 14(2022), 11, p 2740 (DE-627)614095670 (DE-600)2527080-1 20726694 nnns volume:14 year:2022 number:11, p 2740 https://doi.org/10.3390/cancers14112740 kostenfrei https://doaj.org/article/2698dba378ab4534840ad8411061bc53 kostenfrei https://www.mdpi.com/2072-6694/14/11/2740 kostenfrei https://doaj.org/toc/2072-6694 Journal toc kostenfrei GBV_USEFLAG_A SYSFLAG_A GBV_DOAJ 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_2005 GBV_ILN_2009 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2055 GBV_ILN_2111 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 14 2022 11, p 2740
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allfieldsGer	10.3390/cancers14112740 doi (DE-627)DOAJ022410759 (DE-599)DOAJ2698dba378ab4534840ad8411061bc53 DE-627 ger DE-627 rakwb eng RC254-282 Ana Belén Herrera-Campos verfasserin aut Implications of Hyperoxia over the Tumor Microenvironment: An Overview Highlighting the Importance of the Immune System 2022 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Hyperoxia is used in order to counteract hypoxia effects in the TME (tumor microenvironment), which are described to boost the malignant tumor phenotype and poor prognosis. The reduction of tumor hypoxic state through the formation of a non-aberrant vasculature or an increase in the toxicity of the therapeutic agent improves the efficacy of therapies such as chemotherapy. Radiotherapy efficacy has also improved, where apoptotic mechanisms seem to be implicated. Moreover, hyperoxia increases the antitumor immunity through diverse pathways, leading to an immunopermissive TME. Although hyperoxia is an approved treatment for preventing and treating hypoxemia, it has harmful side-effects. Prolonged exposure to high oxygen levels may cause acute lung injury, characterized by an exacerbated immune response, and the destruction of the alveolar–capillary barrier. Furthermore, under this situation, the high concentration of ROS may cause toxicity that will lead not only to cell death but also to an increase in chemoattractant and proinflammatory cytokine secretion. This would end in a lung leukocyte recruitment and, therefore, lung damage. Moreover, unregulated inflammation causes different consequences promoting tumor development and metastasis. This process is known as protumor inflammation, where different cell types and molecules are implicated; for instance, IL-1β has been described as a key cytokine. Although current results show benefits over cancer therapies using hyperoxia, further studies need to be conducted, not only to improve tumor regression, but also to prevent its collateral damage. tumor microenvironment hypoxia hyperoxia immunotherapy inflammation Neoplasms. Tumors. Oncology. Including cancer and carcinogens Esteban Zamudio-Martinez verfasserin aut Daniel Delgado-Bellido verfasserin aut Mónica Fernández-Cortés verfasserin aut Luis M. Montuenga verfasserin aut F. Javier Oliver verfasserin aut Angel Garcia-Diaz verfasserin aut In Cancers MDPI AG, 2010 14(2022), 11, p 2740 (DE-627)614095670 (DE-600)2527080-1 20726694 nnns volume:14 year:2022 number:11, p 2740 https://doi.org/10.3390/cancers14112740 kostenfrei https://doaj.org/article/2698dba378ab4534840ad8411061bc53 kostenfrei https://www.mdpi.com/2072-6694/14/11/2740 kostenfrei https://doaj.org/toc/2072-6694 Journal toc kostenfrei GBV_USEFLAG_A SYSFLAG_A GBV_DOAJ 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_2005 GBV_ILN_2009 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2055 GBV_ILN_2111 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 14 2022 11, p 2740
allfieldsSound	10.3390/cancers14112740 doi (DE-627)DOAJ022410759 (DE-599)DOAJ2698dba378ab4534840ad8411061bc53 DE-627 ger DE-627 rakwb eng RC254-282 Ana Belén Herrera-Campos verfasserin aut Implications of Hyperoxia over the Tumor Microenvironment: An Overview Highlighting the Importance of the Immune System 2022 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Hyperoxia is used in order to counteract hypoxia effects in the TME (tumor microenvironment), which are described to boost the malignant tumor phenotype and poor prognosis. The reduction of tumor hypoxic state through the formation of a non-aberrant vasculature or an increase in the toxicity of the therapeutic agent improves the efficacy of therapies such as chemotherapy. Radiotherapy efficacy has also improved, where apoptotic mechanisms seem to be implicated. Moreover, hyperoxia increases the antitumor immunity through diverse pathways, leading to an immunopermissive TME. Although hyperoxia is an approved treatment for preventing and treating hypoxemia, it has harmful side-effects. Prolonged exposure to high oxygen levels may cause acute lung injury, characterized by an exacerbated immune response, and the destruction of the alveolar–capillary barrier. Furthermore, under this situation, the high concentration of ROS may cause toxicity that will lead not only to cell death but also to an increase in chemoattractant and proinflammatory cytokine secretion. This would end in a lung leukocyte recruitment and, therefore, lung damage. Moreover, unregulated inflammation causes different consequences promoting tumor development and metastasis. This process is known as protumor inflammation, where different cell types and molecules are implicated; for instance, IL-1β has been described as a key cytokine. Although current results show benefits over cancer therapies using hyperoxia, further studies need to be conducted, not only to improve tumor regression, but also to prevent its collateral damage. tumor microenvironment hypoxia hyperoxia immunotherapy inflammation Neoplasms. Tumors. Oncology. Including cancer and carcinogens Esteban Zamudio-Martinez verfasserin aut Daniel Delgado-Bellido verfasserin aut Mónica Fernández-Cortés verfasserin aut Luis M. Montuenga verfasserin aut F. Javier Oliver verfasserin aut Angel Garcia-Diaz verfasserin aut In Cancers MDPI AG, 2010 14(2022), 11, p 2740 (DE-627)614095670 (DE-600)2527080-1 20726694 nnns volume:14 year:2022 number:11, p 2740 https://doi.org/10.3390/cancers14112740 kostenfrei https://doaj.org/article/2698dba378ab4534840ad8411061bc53 kostenfrei https://www.mdpi.com/2072-6694/14/11/2740 kostenfrei https://doaj.org/toc/2072-6694 Journal toc kostenfrei GBV_USEFLAG_A SYSFLAG_A GBV_DOAJ 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_2005 GBV_ILN_2009 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2055 GBV_ILN_2111 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 14 2022 11, p 2740
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topic_facet	tumor microenvironment hypoxia hyperoxia immunotherapy inflammation Neoplasms. Tumors. Oncology. Including cancer and carcinogens
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callnumber-first	R - Medicine
author	Ana Belén Herrera-Campos
spellingShingle	Ana Belén Herrera-Campos misc RC254-282 misc tumor microenvironment misc hypoxia misc hyperoxia misc immunotherapy misc inflammation misc Neoplasms. Tumors. Oncology. Including cancer and carcinogens Implications of Hyperoxia over the Tumor Microenvironment: An Overview Highlighting the Importance of the Immune System
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topic_title	RC254-282 Implications of Hyperoxia over the Tumor Microenvironment: An Overview Highlighting the Importance of the Immune System tumor microenvironment hypoxia hyperoxia immunotherapy inflammation
topic	misc RC254-282 misc tumor microenvironment misc hypoxia misc hyperoxia misc immunotherapy misc inflammation misc Neoplasms. Tumors. Oncology. Including cancer and carcinogens
topic_unstemmed	misc RC254-282 misc tumor microenvironment misc hypoxia misc hyperoxia misc immunotherapy misc inflammation misc Neoplasms. Tumors. Oncology. Including cancer and carcinogens
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title	Implications of Hyperoxia over the Tumor Microenvironment: An Overview Highlighting the Importance of the Immune System
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title_auth	Implications of Hyperoxia over the Tumor Microenvironment: An Overview Highlighting the Importance of the Immune System
abstract	Hyperoxia is used in order to counteract hypoxia effects in the TME (tumor microenvironment), which are described to boost the malignant tumor phenotype and poor prognosis. The reduction of tumor hypoxic state through the formation of a non-aberrant vasculature or an increase in the toxicity of the therapeutic agent improves the efficacy of therapies such as chemotherapy. Radiotherapy efficacy has also improved, where apoptotic mechanisms seem to be implicated. Moreover, hyperoxia increases the antitumor immunity through diverse pathways, leading to an immunopermissive TME. Although hyperoxia is an approved treatment for preventing and treating hypoxemia, it has harmful side-effects. Prolonged exposure to high oxygen levels may cause acute lung injury, characterized by an exacerbated immune response, and the destruction of the alveolar–capillary barrier. Furthermore, under this situation, the high concentration of ROS may cause toxicity that will lead not only to cell death but also to an increase in chemoattractant and proinflammatory cytokine secretion. This would end in a lung leukocyte recruitment and, therefore, lung damage. Moreover, unregulated inflammation causes different consequences promoting tumor development and metastasis. This process is known as protumor inflammation, where different cell types and molecules are implicated; for instance, IL-1β has been described as a key cytokine. Although current results show benefits over cancer therapies using hyperoxia, further studies need to be conducted, not only to improve tumor regression, but also to prevent its collateral damage.
abstractGer	Hyperoxia is used in order to counteract hypoxia effects in the TME (tumor microenvironment), which are described to boost the malignant tumor phenotype and poor prognosis. The reduction of tumor hypoxic state through the formation of a non-aberrant vasculature or an increase in the toxicity of the therapeutic agent improves the efficacy of therapies such as chemotherapy. Radiotherapy efficacy has also improved, where apoptotic mechanisms seem to be implicated. Moreover, hyperoxia increases the antitumor immunity through diverse pathways, leading to an immunopermissive TME. Although hyperoxia is an approved treatment for preventing and treating hypoxemia, it has harmful side-effects. Prolonged exposure to high oxygen levels may cause acute lung injury, characterized by an exacerbated immune response, and the destruction of the alveolar–capillary barrier. Furthermore, under this situation, the high concentration of ROS may cause toxicity that will lead not only to cell death but also to an increase in chemoattractant and proinflammatory cytokine secretion. This would end in a lung leukocyte recruitment and, therefore, lung damage. Moreover, unregulated inflammation causes different consequences promoting tumor development and metastasis. This process is known as protumor inflammation, where different cell types and molecules are implicated; for instance, IL-1β has been described as a key cytokine. Although current results show benefits over cancer therapies using hyperoxia, further studies need to be conducted, not only to improve tumor regression, but also to prevent its collateral damage.
abstract_unstemmed	Hyperoxia is used in order to counteract hypoxia effects in the TME (tumor microenvironment), which are described to boost the malignant tumor phenotype and poor prognosis. The reduction of tumor hypoxic state through the formation of a non-aberrant vasculature or an increase in the toxicity of the therapeutic agent improves the efficacy of therapies such as chemotherapy. Radiotherapy efficacy has also improved, where apoptotic mechanisms seem to be implicated. Moreover, hyperoxia increases the antitumor immunity through diverse pathways, leading to an immunopermissive TME. Although hyperoxia is an approved treatment for preventing and treating hypoxemia, it has harmful side-effects. Prolonged exposure to high oxygen levels may cause acute lung injury, characterized by an exacerbated immune response, and the destruction of the alveolar–capillary barrier. Furthermore, under this situation, the high concentration of ROS may cause toxicity that will lead not only to cell death but also to an increase in chemoattractant and proinflammatory cytokine secretion. This would end in a lung leukocyte recruitment and, therefore, lung damage. Moreover, unregulated inflammation causes different consequences promoting tumor development and metastasis. This process is known as protumor inflammation, where different cell types and molecules are implicated; for instance, IL-1β has been described as a key cytokine. Although current results show benefits over cancer therapies using hyperoxia, further studies need to be conducted, not only to improve tumor regression, but also to prevent its collateral damage.
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Implications of Hyperoxia over the Tumor Microenvironment: An Overview Highlighting the Importance of the Immune System

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