Aldehyde dehydrogenases in cellular responses to oxidative/electrophilic stress
Reactive oxygen species (ROS) are continuously generated within living systems and the inability to manage ROS load leads to elevated oxidative stress and cell damage. Oxidative stress is coupled to the oxidative degradation of lipid membranes, also known as lipid peroxidation. This process generate...
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Veröffentlicht in: | Free radical biology & medicine 2013-03, Vol.56, p.89-101 |
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description | Reactive oxygen species (ROS) are continuously generated within living systems and the inability to manage ROS load leads to elevated oxidative stress and cell damage. Oxidative stress is coupled to the oxidative degradation of lipid membranes, also known as lipid peroxidation. This process generates over 200 types of aldehydes, many of which are highly reactive and toxic. Aldehyde dehydrogenases (ALDHs) metabolize endogenous and exogenous aldehydes and thereby mitigate oxidative/electrophilic stress in prokaryotic and eukaryotic organisms. ALDHs are found throughout the evolutionary gamut, from single-celled organisms to complex multicellular species. Not surprisingly, many ALDHs in evolutionarily distant, and seemingly unrelated, species perform similar functions, including protection against a variety of environmental stressors such as dehydration and ultraviolet radiation. The ability to act as an "aldehyde scavenger" during lipid peroxidation is another ostensibly universal ALDH function found across species. Upregulation of ALDHs is a stress response in bacteria (environmental and chemical stress), plants (dehydration, salinity, and oxidative stress), yeast (ethanol exposure and oxidative stress), Caenorhabditis elegans (lipid peroxidation), and mammals (oxidative stress and lipid peroxidation). Recent studies have also identified ALDH activity as an important feature of cancer stem cells. In these cells, ALDH expression helps abrogate oxidative stress and imparts resistance against chemotherapeutic agents such as oxazaphosphorine, taxane, and platinum drugs. The ALDH superfamily represents a fundamentally important class of enzymes that contributes significantly to the management of electrophilic/oxidative stress within living systems. Mutations in various ALDHs are associated with a variety of pathological conditions in humans, highlighting the fundamental importance of these enzymes in physiological and pathological processes. |
doi_str_mv | 10.1016/j.freeradbiomed.2012.11.010 |
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Oxidative stress is coupled to the oxidative degradation of lipid membranes, also known as lipid peroxidation. This process generates over 200 types of aldehydes, many of which are highly reactive and toxic. Aldehyde dehydrogenases (ALDHs) metabolize endogenous and exogenous aldehydes and thereby mitigate oxidative/electrophilic stress in prokaryotic and eukaryotic organisms. ALDHs are found throughout the evolutionary gamut, from single-celled organisms to complex multicellular species. Not surprisingly, many ALDHs in evolutionarily distant, and seemingly unrelated, species perform similar functions, including protection against a variety of environmental stressors such as dehydration and ultraviolet radiation. The ability to act as an "aldehyde scavenger" during lipid peroxidation is another ostensibly universal ALDH function found across species. Upregulation of ALDHs is a stress response in bacteria (environmental and chemical stress), plants (dehydration, salinity, and oxidative stress), yeast (ethanol exposure and oxidative stress), Caenorhabditis elegans (lipid peroxidation), and mammals (oxidative stress and lipid peroxidation). Recent studies have also identified ALDH activity as an important feature of cancer stem cells. In these cells, ALDH expression helps abrogate oxidative stress and imparts resistance against chemotherapeutic agents such as oxazaphosphorine, taxane, and platinum drugs. The ALDH superfamily represents a fundamentally important class of enzymes that contributes significantly to the management of electrophilic/oxidative stress within living systems. Mutations in various ALDHs are associated with a variety of pathological conditions in humans, highlighting the fundamental importance of these enzymes in physiological and pathological processes.</description><identifier>ISSN: 0891-5849</identifier><identifier>EISSN: 1873-4596</identifier><identifier>DOI: 10.1016/j.freeradbiomed.2012.11.010</identifier><identifier>PMID: 23195683</identifier><language>eng</language><publisher>United States</publisher><subject>Aldehyde Dehydrogenase - genetics ; Aldehyde Dehydrogenase - metabolism ; Animals ; Bacteria - enzymology ; Bacteria - metabolism ; Caenorhabditis elegans - enzymology ; Caenorhabditis elegans - metabolism ; Humans ; Neoplastic Stem Cells - enzymology ; Neoplastic Stem Cells - metabolism ; Oxidative Stress ; Plants - enzymology ; Plants - metabolism ; Reactive Oxygen Species - metabolism ; Saccharomyces cerevisiae - enzymology ; Saccharomyces cerevisiae - metabolism</subject><ispartof>Free radical biology & medicine, 2013-03, Vol.56, p.89-101</ispartof><rights>Copyright © 2012 Elsevier Inc. All rights reserved.</rights><rights>2012 Elsevier Inc. All rights reserved. 2012</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c254t-a329c51ad28fb9bc1a83accc9642c26edc19957b0f3893d327669d85734371013</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,780,784,885,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/23195683$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Singh, Surendra</creatorcontrib><creatorcontrib>Brocker, Chad</creatorcontrib><creatorcontrib>Koppaka, Vindhya</creatorcontrib><creatorcontrib>Chen, Ying</creatorcontrib><creatorcontrib>Jackson, Brian C</creatorcontrib><creatorcontrib>Matsumoto, Akiko</creatorcontrib><creatorcontrib>Thompson, David C</creatorcontrib><creatorcontrib>Vasiliou, Vasilis</creatorcontrib><title>Aldehyde dehydrogenases in cellular responses to oxidative/electrophilic stress</title><title>Free radical biology & medicine</title><addtitle>Free Radic Biol Med</addtitle><description>Reactive oxygen species (ROS) are continuously generated within living systems and the inability to manage ROS load leads to elevated oxidative stress and cell damage. Oxidative stress is coupled to the oxidative degradation of lipid membranes, also known as lipid peroxidation. This process generates over 200 types of aldehydes, many of which are highly reactive and toxic. Aldehyde dehydrogenases (ALDHs) metabolize endogenous and exogenous aldehydes and thereby mitigate oxidative/electrophilic stress in prokaryotic and eukaryotic organisms. ALDHs are found throughout the evolutionary gamut, from single-celled organisms to complex multicellular species. Not surprisingly, many ALDHs in evolutionarily distant, and seemingly unrelated, species perform similar functions, including protection against a variety of environmental stressors such as dehydration and ultraviolet radiation. The ability to act as an "aldehyde scavenger" during lipid peroxidation is another ostensibly universal ALDH function found across species. Upregulation of ALDHs is a stress response in bacteria (environmental and chemical stress), plants (dehydration, salinity, and oxidative stress), yeast (ethanol exposure and oxidative stress), Caenorhabditis elegans (lipid peroxidation), and mammals (oxidative stress and lipid peroxidation). Recent studies have also identified ALDH activity as an important feature of cancer stem cells. In these cells, ALDH expression helps abrogate oxidative stress and imparts resistance against chemotherapeutic agents such as oxazaphosphorine, taxane, and platinum drugs. The ALDH superfamily represents a fundamentally important class of enzymes that contributes significantly to the management of electrophilic/oxidative stress within living systems. Mutations in various ALDHs are associated with a variety of pathological conditions in humans, highlighting the fundamental importance of these enzymes in physiological and pathological processes.</description><subject>Aldehyde Dehydrogenase - genetics</subject><subject>Aldehyde Dehydrogenase - metabolism</subject><subject>Animals</subject><subject>Bacteria - enzymology</subject><subject>Bacteria - metabolism</subject><subject>Caenorhabditis elegans - enzymology</subject><subject>Caenorhabditis elegans - metabolism</subject><subject>Humans</subject><subject>Neoplastic Stem Cells - enzymology</subject><subject>Neoplastic Stem Cells - metabolism</subject><subject>Oxidative Stress</subject><subject>Plants - enzymology</subject><subject>Plants - metabolism</subject><subject>Reactive Oxygen Species - metabolism</subject><subject>Saccharomyces cerevisiae - enzymology</subject><subject>Saccharomyces cerevisiae - metabolism</subject><issn>0891-5849</issn><issn>1873-4596</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpVkF1LwzAUhoMobk7_ghS8bpfkNGlyI4zhFwx2o9clTdItI2tKUof799ZP9OqF9z3nuXgQuiG4IJjw-a5oo7VRmcaFvTUFxYQWhBSY4BM0JaKCvGSSn6IpFpLkTJRygi5S2mGMSwbiHE0oEMm4gClaL7yx26Ox2WfEsLGdSjZlrsu09f7Vq5hFm_rQfbRDyMKbM2pwBzu33uohhn7rvNNZGsazdInOWuWTvfrOGXq5v3tePuar9cPTcrHKNWXlkCugUjOiDBVtIxtNlACltZa8pJpyazSRklUNbkFIMEArzqURrIISqtECzNDtF7d_bUYJ2nZDVL7uo9ureKyDcvX_pXPbehMONXAgwPAIuP4L-P38UQPvcvpteQ</recordid><startdate>20130301</startdate><enddate>20130301</enddate><creator>Singh, Surendra</creator><creator>Brocker, Chad</creator><creator>Koppaka, Vindhya</creator><creator>Chen, Ying</creator><creator>Jackson, Brian C</creator><creator>Matsumoto, Akiko</creator><creator>Thompson, David C</creator><creator>Vasiliou, Vasilis</creator><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>5PM</scope></search><sort><creationdate>20130301</creationdate><title>Aldehyde dehydrogenases in cellular responses to oxidative/electrophilic stress</title><author>Singh, Surendra ; Brocker, Chad ; Koppaka, Vindhya ; Chen, Ying ; Jackson, Brian C ; Matsumoto, Akiko ; Thompson, David C ; Vasiliou, Vasilis</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c254t-a329c51ad28fb9bc1a83accc9642c26edc19957b0f3893d327669d85734371013</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2013</creationdate><topic>Aldehyde Dehydrogenase - genetics</topic><topic>Aldehyde Dehydrogenase - metabolism</topic><topic>Animals</topic><topic>Bacteria - enzymology</topic><topic>Bacteria - metabolism</topic><topic>Caenorhabditis elegans - enzymology</topic><topic>Caenorhabditis elegans - metabolism</topic><topic>Humans</topic><topic>Neoplastic Stem Cells - enzymology</topic><topic>Neoplastic Stem Cells - metabolism</topic><topic>Oxidative Stress</topic><topic>Plants - enzymology</topic><topic>Plants - metabolism</topic><topic>Reactive Oxygen Species - metabolism</topic><topic>Saccharomyces cerevisiae - enzymology</topic><topic>Saccharomyces cerevisiae - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Singh, Surendra</creatorcontrib><creatorcontrib>Brocker, Chad</creatorcontrib><creatorcontrib>Koppaka, Vindhya</creatorcontrib><creatorcontrib>Chen, Ying</creatorcontrib><creatorcontrib>Jackson, Brian C</creatorcontrib><creatorcontrib>Matsumoto, Akiko</creatorcontrib><creatorcontrib>Thompson, David C</creatorcontrib><creatorcontrib>Vasiliou, Vasilis</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Free radical biology & medicine</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Singh, Surendra</au><au>Brocker, Chad</au><au>Koppaka, Vindhya</au><au>Chen, Ying</au><au>Jackson, Brian C</au><au>Matsumoto, Akiko</au><au>Thompson, David C</au><au>Vasiliou, Vasilis</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Aldehyde dehydrogenases in cellular responses to oxidative/electrophilic stress</atitle><jtitle>Free radical biology & medicine</jtitle><addtitle>Free Radic Biol Med</addtitle><date>2013-03-01</date><risdate>2013</risdate><volume>56</volume><spage>89</spage><epage>101</epage><pages>89-101</pages><issn>0891-5849</issn><eissn>1873-4596</eissn><abstract>Reactive oxygen species (ROS) are continuously generated within living systems and the inability to manage ROS load leads to elevated oxidative stress and cell damage. Oxidative stress is coupled to the oxidative degradation of lipid membranes, also known as lipid peroxidation. This process generates over 200 types of aldehydes, many of which are highly reactive and toxic. Aldehyde dehydrogenases (ALDHs) metabolize endogenous and exogenous aldehydes and thereby mitigate oxidative/electrophilic stress in prokaryotic and eukaryotic organisms. ALDHs are found throughout the evolutionary gamut, from single-celled organisms to complex multicellular species. Not surprisingly, many ALDHs in evolutionarily distant, and seemingly unrelated, species perform similar functions, including protection against a variety of environmental stressors such as dehydration and ultraviolet radiation. The ability to act as an "aldehyde scavenger" during lipid peroxidation is another ostensibly universal ALDH function found across species. Upregulation of ALDHs is a stress response in bacteria (environmental and chemical stress), plants (dehydration, salinity, and oxidative stress), yeast (ethanol exposure and oxidative stress), Caenorhabditis elegans (lipid peroxidation), and mammals (oxidative stress and lipid peroxidation). Recent studies have also identified ALDH activity as an important feature of cancer stem cells. In these cells, ALDH expression helps abrogate oxidative stress and imparts resistance against chemotherapeutic agents such as oxazaphosphorine, taxane, and platinum drugs. The ALDH superfamily represents a fundamentally important class of enzymes that contributes significantly to the management of electrophilic/oxidative stress within living systems. Mutations in various ALDHs are associated with a variety of pathological conditions in humans, highlighting the fundamental importance of these enzymes in physiological and pathological processes.</abstract><cop>United States</cop><pmid>23195683</pmid><doi>10.1016/j.freeradbiomed.2012.11.010</doi><tpages>13</tpages></addata></record> |
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subjects | Aldehyde Dehydrogenase - genetics Aldehyde Dehydrogenase - metabolism Animals Bacteria - enzymology Bacteria - metabolism Caenorhabditis elegans - enzymology Caenorhabditis elegans - metabolism Humans Neoplastic Stem Cells - enzymology Neoplastic Stem Cells - metabolism Oxidative Stress Plants - enzymology Plants - metabolism Reactive Oxygen Species - metabolism Saccharomyces cerevisiae - enzymology Saccharomyces cerevisiae - metabolism |
title | Aldehyde dehydrogenases in cellular responses to oxidative/electrophilic stress |
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