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Reactive Oxygen Species: A Key Constituent in Cancer Survival
Background: Cancer is one of the major heterogeneous disease with high morbidity and mortality with poor prognosis. Elevated levels of reactive oxygen species (ROS), alteration in redox balance, and deregulated redox signaling are common hallmarks of cancer progression and resistance to treatment. M...
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Published in: | Biomarker Insights 2018, Vol.13, p.1177271918755391-1177271918755391 |
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description | Background:
Cancer is one of the major heterogeneous disease with high morbidity and mortality with poor prognosis. Elevated levels of reactive oxygen species (ROS), alteration in redox balance, and deregulated redox signaling are common hallmarks of cancer progression and resistance to treatment. Mitochondria contribute mainly in the generation of ROS during oxidative phosphorylation. Elevated levels of ROS have been detected in cancers cells due to high metabolic activity, cellular signaling, peroxisomal activity, mitochondrial dysfunction, activation of oncogene, and increased enzymatic activity of oxidases, cyclooxygenases, lipoxygenases, and thymidine phosphorylases. Cells maintain intracellular homeostasis by developing an immense antioxidant system including catalase, superoxide dismutase, and glutathione peroxidase. Besides these enzymes exist an important antioxidant glutathione and transcription factor Nrf2 which contribute in balancing oxidative stress. Reactive oxygen species–mediated signaling pathways activate pro-oncogenic signaling which eases in cancer progression, angiogenesis, and survival. Concomitantly, to maintain ROS homeostasis and evade cancer cell death, an increased level of antioxidant capacity is associated with cancer cells.
Conclusions:
This review focuses the role of ROS in cancer survival pathways and importance of targeting the ROS signal involved in cancer development, which is a new strategy in cancer treatment. |
doi_str_mv | 10.1177/1177271918755391 |
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Cancer is one of the major heterogeneous disease with high morbidity and mortality with poor prognosis. Elevated levels of reactive oxygen species (ROS), alteration in redox balance, and deregulated redox signaling are common hallmarks of cancer progression and resistance to treatment. Mitochondria contribute mainly in the generation of ROS during oxidative phosphorylation. Elevated levels of ROS have been detected in cancers cells due to high metabolic activity, cellular signaling, peroxisomal activity, mitochondrial dysfunction, activation of oncogene, and increased enzymatic activity of oxidases, cyclooxygenases, lipoxygenases, and thymidine phosphorylases. Cells maintain intracellular homeostasis by developing an immense antioxidant system including catalase, superoxide dismutase, and glutathione peroxidase. Besides these enzymes exist an important antioxidant glutathione and transcription factor Nrf2 which contribute in balancing oxidative stress. Reactive oxygen species–mediated signaling pathways activate pro-oncogenic signaling which eases in cancer progression, angiogenesis, and survival. Concomitantly, to maintain ROS homeostasis and evade cancer cell death, an increased level of antioxidant capacity is associated with cancer cells.
Conclusions:
This review focuses the role of ROS in cancer survival pathways and importance of targeting the ROS signal involved in cancer development, which is a new strategy in cancer treatment.</description><identifier>ISSN: 1177-2719</identifier><identifier>EISSN: 1177-2719</identifier><identifier>DOI: 10.1177/1177271918755391</identifier><identifier>PMID: 29449774</identifier><language>eng</language><publisher>London, England: SAGE Publications</publisher><subject>Angiogenesis ; Antioxidants ; Authorship ; Binding sites ; Cancer ; Catalase ; Cell adhesion & migration ; Cell death ; Cell division ; Enzymatic activity ; Enzymes ; Extracellular matrix ; Fatty acids ; Free radicals ; Glutathione peroxidase ; Homeostasis ; Hydrogen peroxide ; Medical prognosis ; Membranes ; Metabolism ; Metabolites ; Metastasis ; Mitochondria ; Morbidity ; Mortality ; Nitric oxide ; Nitrogen dioxide ; Oxidative phosphorylation ; Oxidative stress ; Permeability ; Phosphorylation ; Reactive oxygen species ; Review ; Signal transduction ; Species ; Superoxide dismutase ; Thymidine</subject><ispartof>Biomarker Insights, 2018, Vol.13, p.1177271918755391-1177271918755391</ispartof><rights>The Author(s) 2018</rights><rights>2018. This work is published under http://creativecommons.org/licenses/by-nc/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>The Author(s) 2018. This work is licensed under the Creative Commons Attribution – Non-Commercial License http://creativecommons.org/licenses/by-nc/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>The Author(s) 2018 2018 SAGE Publications Ltd unless otherwise noted. Manuscript content on this site is licensed under Creative Commons Licenses</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c622t-1838fa2f0d3d0dc8e7f97fcde128ebc476bbea7eda3533d7307faf54691826a03</citedby><cites>FETCH-LOGICAL-c622t-1838fa2f0d3d0dc8e7f97fcde128ebc476bbea7eda3533d7307faf54691826a03</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC5808965/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/2171101759?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,313,314,727,780,784,792,885,4024,4054,21966,25753,27853,27922,27923,27924,27925,37012,37013,44590,44945,45333,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/29449774$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Kumari, Seema</creatorcontrib><creatorcontrib>Badana, Anil Kumar</creatorcontrib><creatorcontrib>G, Murali Mohan</creatorcontrib><creatorcontrib>G, Shailender</creatorcontrib><creatorcontrib>Malla, RamaRao</creatorcontrib><title>Reactive Oxygen Species: A Key Constituent in Cancer Survival</title><title>Biomarker Insights</title><addtitle>Biomark Insights</addtitle><description>Background:
Cancer is one of the major heterogeneous disease with high morbidity and mortality with poor prognosis. Elevated levels of reactive oxygen species (ROS), alteration in redox balance, and deregulated redox signaling are common hallmarks of cancer progression and resistance to treatment. Mitochondria contribute mainly in the generation of ROS during oxidative phosphorylation. Elevated levels of ROS have been detected in cancers cells due to high metabolic activity, cellular signaling, peroxisomal activity, mitochondrial dysfunction, activation of oncogene, and increased enzymatic activity of oxidases, cyclooxygenases, lipoxygenases, and thymidine phosphorylases. Cells maintain intracellular homeostasis by developing an immense antioxidant system including catalase, superoxide dismutase, and glutathione peroxidase. Besides these enzymes exist an important antioxidant glutathione and transcription factor Nrf2 which contribute in balancing oxidative stress. Reactive oxygen species–mediated signaling pathways activate pro-oncogenic signaling which eases in cancer progression, angiogenesis, and survival. Concomitantly, to maintain ROS homeostasis and evade cancer cell death, an increased level of antioxidant capacity is associated with cancer cells.
Conclusions:
This review focuses the role of ROS in cancer survival pathways and importance of targeting the ROS signal involved in cancer development, which is a new strategy in cancer treatment.</description><subject>Angiogenesis</subject><subject>Antioxidants</subject><subject>Authorship</subject><subject>Binding sites</subject><subject>Cancer</subject><subject>Catalase</subject><subject>Cell adhesion & migration</subject><subject>Cell death</subject><subject>Cell division</subject><subject>Enzymatic activity</subject><subject>Enzymes</subject><subject>Extracellular matrix</subject><subject>Fatty acids</subject><subject>Free radicals</subject><subject>Glutathione peroxidase</subject><subject>Homeostasis</subject><subject>Hydrogen peroxide</subject><subject>Medical prognosis</subject><subject>Membranes</subject><subject>Metabolism</subject><subject>Metabolites</subject><subject>Metastasis</subject><subject>Mitochondria</subject><subject>Morbidity</subject><subject>Mortality</subject><subject>Nitric oxide</subject><subject>Nitrogen dioxide</subject><subject>Oxidative phosphorylation</subject><subject>Oxidative stress</subject><subject>Permeability</subject><subject>Phosphorylation</subject><subject>Reactive oxygen species</subject><subject>Review</subject><subject>Signal transduction</subject><subject>Species</subject><subject>Superoxide dismutase</subject><subject>Thymidine</subject><issn>1177-2719</issn><issn>1177-2719</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><sourceid>AFRWT</sourceid><sourceid>PIMPY</sourceid><sourceid>DOA</sourceid><recordid>eNp9kttrFDEUxoNYbK2--yQDvvgymvtFsFAWL6WFgtXnkMmcrFlmJ2sys7j_vTNurW2hfUnCl-_8zjk5QegVwe8IUer9vFBFDNFKCGbIE3Q0S_WsPb11PkTPS1lhLKSm-Bk6pIZzoxQ_Qh-_gfND3EJ1-Xu3hL662oCPUD5Up9U57KpF6ssQhxH6oYp9tXC9h1xdjXkbt657gQ6C6wq8vN6P0Y_Pn74vvtYXl1_OFqcXtZeUDjXRTAdHA25Zi1uvQQWjgm-BUA2N50o2DTgFrWOCsVYxrIILgsupMSodZsfobM9tk1vZTY5rl3c2uWj_CikvrctD9B3YRgBljEmjJeaS6UZKAMeIICw0jeQT62TP2ozNGlo_dZZddwd696aPP-0yba3QWBspJsDba0BOv0Yog13H4qHrXA9pLJZizDAnCs-53tyzrtKY--mpLOWUGCaM1I-6iCIEEyXM5MJ7l8-plAzhpmSC7Txpe_83TCGvb7d6E_Bv_JOh3huKW8L_rA8C_wDN3roE</recordid><startdate>2018</startdate><enddate>2018</enddate><creator>Kumari, Seema</creator><creator>Badana, Anil Kumar</creator><creator>G, Murali Mohan</creator><creator>G, Shailender</creator><creator>Malla, RamaRao</creator><general>SAGE Publications</general><general>Sage Publications Ltd</general><general>SAGE Publishing</general><scope>AFRWT</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>8FE</scope><scope>8FH</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AYAGU</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>LK8</scope><scope>M7P</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope></search><sort><creationdate>2018</creationdate><title>Reactive Oxygen Species: A Key Constituent in Cancer Survival</title><author>Kumari, Seema ; Badana, Anil Kumar ; G, Murali Mohan ; G, Shailender ; Malla, RamaRao</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c622t-1838fa2f0d3d0dc8e7f97fcde128ebc476bbea7eda3533d7307faf54691826a03</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2018</creationdate><topic>Angiogenesis</topic><topic>Antioxidants</topic><topic>Authorship</topic><topic>Binding sites</topic><topic>Cancer</topic><topic>Catalase</topic><topic>Cell adhesion & migration</topic><topic>Cell death</topic><topic>Cell division</topic><topic>Enzymatic activity</topic><topic>Enzymes</topic><topic>Extracellular matrix</topic><topic>Fatty acids</topic><topic>Free radicals</topic><topic>Glutathione peroxidase</topic><topic>Homeostasis</topic><topic>Hydrogen peroxide</topic><topic>Medical prognosis</topic><topic>Membranes</topic><topic>Metabolism</topic><topic>Metabolites</topic><topic>Metastasis</topic><topic>Mitochondria</topic><topic>Morbidity</topic><topic>Mortality</topic><topic>Nitric oxide</topic><topic>Nitrogen dioxide</topic><topic>Oxidative phosphorylation</topic><topic>Oxidative stress</topic><topic>Permeability</topic><topic>Phosphorylation</topic><topic>Reactive oxygen species</topic><topic>Review</topic><topic>Signal transduction</topic><topic>Species</topic><topic>Superoxide dismutase</topic><topic>Thymidine</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kumari, Seema</creatorcontrib><creatorcontrib>Badana, Anil Kumar</creatorcontrib><creatorcontrib>G, Murali Mohan</creatorcontrib><creatorcontrib>G, Shailender</creatorcontrib><creatorcontrib>Malla, RamaRao</creatorcontrib><collection>SAGE Journals</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>Australia & New Zealand Database</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Biological Science Collection</collection><collection>Biological Science Database</collection><collection>Publicly Available Content Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>Biomarker Insights</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kumari, Seema</au><au>Badana, Anil Kumar</au><au>G, Murali Mohan</au><au>G, Shailender</au><au>Malla, RamaRao</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Reactive Oxygen Species: A Key Constituent in Cancer Survival</atitle><jtitle>Biomarker Insights</jtitle><addtitle>Biomark Insights</addtitle><date>2018</date><risdate>2018</risdate><volume>13</volume><spage>1177271918755391</spage><epage>1177271918755391</epage><pages>1177271918755391-1177271918755391</pages><issn>1177-2719</issn><eissn>1177-2719</eissn><abstract>Background:
Cancer is one of the major heterogeneous disease with high morbidity and mortality with poor prognosis. Elevated levels of reactive oxygen species (ROS), alteration in redox balance, and deregulated redox signaling are common hallmarks of cancer progression and resistance to treatment. Mitochondria contribute mainly in the generation of ROS during oxidative phosphorylation. Elevated levels of ROS have been detected in cancers cells due to high metabolic activity, cellular signaling, peroxisomal activity, mitochondrial dysfunction, activation of oncogene, and increased enzymatic activity of oxidases, cyclooxygenases, lipoxygenases, and thymidine phosphorylases. Cells maintain intracellular homeostasis by developing an immense antioxidant system including catalase, superoxide dismutase, and glutathione peroxidase. Besides these enzymes exist an important antioxidant glutathione and transcription factor Nrf2 which contribute in balancing oxidative stress. Reactive oxygen species–mediated signaling pathways activate pro-oncogenic signaling which eases in cancer progression, angiogenesis, and survival. Concomitantly, to maintain ROS homeostasis and evade cancer cell death, an increased level of antioxidant capacity is associated with cancer cells.
Conclusions:
This review focuses the role of ROS in cancer survival pathways and importance of targeting the ROS signal involved in cancer development, which is a new strategy in cancer treatment.</abstract><cop>London, England</cop><pub>SAGE Publications</pub><pmid>29449774</pmid><doi>10.1177/1177271918755391</doi><oa>free_for_read</oa></addata></record> |
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subjects | Angiogenesis Antioxidants Authorship Binding sites Cancer Catalase Cell adhesion & migration Cell death Cell division Enzymatic activity Enzymes Extracellular matrix Fatty acids Free radicals Glutathione peroxidase Homeostasis Hydrogen peroxide Medical prognosis Membranes Metabolism Metabolites Metastasis Mitochondria Morbidity Mortality Nitric oxide Nitrogen dioxide Oxidative phosphorylation Oxidative stress Permeability Phosphorylation Reactive oxygen species Review Signal transduction Species Superoxide dismutase Thymidine |
title | Reactive Oxygen Species: A Key Constituent in Cancer Survival |
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