Selenoprotein deficiency enhances radiation-induced micronuclei formation
The availability of selenium and the levels of specific selenoproteins might affect cancer risk by influencing the ability of DNA damaging agents to cause genomic instability and mutations. Transgenic mice that express reduced levels of selenoproteins and previously shown to be more susceptible to p...
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Veröffentlicht in: | Molecular nutrition & food research 2008-11, Vol.52 (11), p.1300-1304 |
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creator | Baliga, Manjeshwar S Diwadkar-Navsariwala, Veda Koh, Timothy Fayad, Raja Fantuzzi, Giamila Diamond, Alan M |
description | The availability of selenium and the levels of specific selenoproteins might affect cancer risk by influencing the ability of DNA damaging agents to cause genomic instability and mutations. Transgenic mice that express reduced levels of selenoproteins and previously shown to be more susceptible to pathology associated with cancer development were used to study this possibility. These mice were exposed to X-rays and DNA damage assessed in the erythrocytes, where micronuclei formation was higher compared to the same cells obtained from irradiated wild-type controls. To determine whether the selenoprotein glutathione peroxidase-1 (GPx-1) might be involved in this protection, its levels were reduced by siRNA targeting in LNCaP human prostate cells. UV-induced micronuclei frequency was higher in these cells compared to control-transfected cells. These results indicate a role for selenoproteins in protecting DNA from damage and support human data implicating GPx-1 as a possible target of the chemoprotective effect of selenium. |
doi_str_mv | 10.1002/mnfr.200800020 |
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Transgenic mice that express reduced levels of selenoproteins and previously shown to be more susceptible to pathology associated with cancer development were used to study this possibility. These mice were exposed to X-rays and DNA damage assessed in the erythrocytes, where micronuclei formation was higher compared to the same cells obtained from irradiated wild-type controls. To determine whether the selenoprotein glutathione peroxidase-1 (GPx-1) might be involved in this protection, its levels were reduced by siRNA targeting in LNCaP human prostate cells. UV-induced micronuclei frequency was higher in these cells compared to control-transfected cells. These results indicate a role for selenoproteins in protecting DNA from damage and support human data implicating GPx-1 as a possible target of the chemoprotective effect of selenium.</description><identifier>ISSN: 1613-4125</identifier><identifier>EISSN: 1613-4133</identifier><identifier>DOI: 10.1002/mnfr.200800020</identifier><identifier>PMID: 18720346</identifier><language>eng</language><publisher>Weinheim: Wiley-VCH Verlag</publisher><subject>animal disease models ; Animals ; Base Sequence ; chemoprevention ; DNA Damage ; erythrocytes ; glutathione ; Glutathione peroxidase ; Glutathione Peroxidase - metabolism ; Glutathione Peroxidase - radiation effects ; humans ; Mice ; Mice, Transgenic ; Micronucleus, Germline - drug effects ; Micronucleus, Germline - radiation effects ; neoplasms ; nutrient availability ; nutrient deficiencies ; prostate gland ; radiotherapy ; risk ; RNA, Messenger - genetics ; RNA, Small Interfering - genetics ; Selenium ; Selenoproteins ; Selenoproteins - deficiency ; Selenoproteins - metabolism ; Selenoproteins - radiation effects ; small interfering RNA ; transgenic animals ; Ultraviolet Rays ; X-radiation ; X-Rays</subject><ispartof>Molecular nutrition & food research, 2008-11, Vol.52 (11), p.1300-1304</ispartof><rights>Copyright © 2008 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4050-d8a64e1841762fcc524ef72ac2dcb7fa9597344b072db73b4fc30e03dc2b83553</citedby><cites>FETCH-LOGICAL-c4050-d8a64e1841762fcc524ef72ac2dcb7fa9597344b072db73b4fc30e03dc2b83553</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fmnfr.200800020$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fmnfr.200800020$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,780,784,1417,27924,27925,45574,45575</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/18720346$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Baliga, Manjeshwar S</creatorcontrib><creatorcontrib>Diwadkar-Navsariwala, Veda</creatorcontrib><creatorcontrib>Koh, Timothy</creatorcontrib><creatorcontrib>Fayad, Raja</creatorcontrib><creatorcontrib>Fantuzzi, Giamila</creatorcontrib><creatorcontrib>Diamond, Alan M</creatorcontrib><title>Selenoprotein deficiency enhances radiation-induced micronuclei formation</title><title>Molecular nutrition & food research</title><addtitle>Mol. Nutr. Food Res</addtitle><description>The availability of selenium and the levels of specific selenoproteins might affect cancer risk by influencing the ability of DNA damaging agents to cause genomic instability and mutations. Transgenic mice that express reduced levels of selenoproteins and previously shown to be more susceptible to pathology associated with cancer development were used to study this possibility. These mice were exposed to X-rays and DNA damage assessed in the erythrocytes, where micronuclei formation was higher compared to the same cells obtained from irradiated wild-type controls. To determine whether the selenoprotein glutathione peroxidase-1 (GPx-1) might be involved in this protection, its levels were reduced by siRNA targeting in LNCaP human prostate cells. UV-induced micronuclei frequency was higher in these cells compared to control-transfected cells. These results indicate a role for selenoproteins in protecting DNA from damage and support human data implicating GPx-1 as a possible target of the chemoprotective effect of selenium.</description><subject>animal disease models</subject><subject>Animals</subject><subject>Base Sequence</subject><subject>chemoprevention</subject><subject>DNA Damage</subject><subject>erythrocytes</subject><subject>glutathione</subject><subject>Glutathione peroxidase</subject><subject>Glutathione Peroxidase - metabolism</subject><subject>Glutathione Peroxidase - radiation effects</subject><subject>humans</subject><subject>Mice</subject><subject>Mice, Transgenic</subject><subject>Micronucleus, Germline - drug effects</subject><subject>Micronucleus, Germline - radiation effects</subject><subject>neoplasms</subject><subject>nutrient availability</subject><subject>nutrient deficiencies</subject><subject>prostate gland</subject><subject>radiotherapy</subject><subject>risk</subject><subject>RNA, Messenger - genetics</subject><subject>RNA, Small Interfering - genetics</subject><subject>Selenium</subject><subject>Selenoproteins</subject><subject>Selenoproteins - deficiency</subject><subject>Selenoproteins - metabolism</subject><subject>Selenoproteins - radiation effects</subject><subject>small interfering RNA</subject><subject>transgenic animals</subject><subject>Ultraviolet Rays</subject><subject>X-radiation</subject><subject>X-Rays</subject><issn>1613-4125</issn><issn>1613-4133</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2008</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkM1v1DAQxa2qiH7AtUfIiVuW8VecHKuKfkil0G4rerMce0xdEqfYG9H970nJauHGaWY0v_f09Ag5orCgAOxjH31aMIAapgt2yD6tKC8F5Xx3uzO5Rw5yfgTglAn-muzRWjHgotonF0vsMA5PaVhhiIVDH2zAaNcFxgcTLeYiGRfMKgyxDNGNFl3RB5uGONoOQ-GH1P_5viGvvOkyvt3MQ3J3-un25Ly8_HJ2cXJ8WVoBEkpXm0ogrQVVFfPWSibQK2Ysc7ZV3jSyUVyIFhRzreKt8JYDAneWtTWXkh-SD7PvlPnniHml-5Atdp2JOIxZV42qGwrNBC5mcAqbc0Kvn1LoTVprCvqlPP1Snt6WNwnebZzHtkf3F9-0NQHNDPwKHa7_Y6c_X53e_GteztqQV_i81Zr0Q1eKK6m_XZ3p6-X58v72XuqvE_9-5r0ZtPmeQtZ3SwaUA5WyaSrGfwMqWZU0</recordid><startdate>200811</startdate><enddate>200811</enddate><creator>Baliga, Manjeshwar S</creator><creator>Diwadkar-Navsariwala, Veda</creator><creator>Koh, Timothy</creator><creator>Fayad, Raja</creator><creator>Fantuzzi, Giamila</creator><creator>Diamond, Alan M</creator><general>Wiley-VCH Verlag</general><general>WILEY-VCH Verlag</general><general>WILEY‐VCH Verlag</general><scope>FBQ</scope><scope>BSCLL</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>200811</creationdate><title>Selenoprotein deficiency enhances radiation-induced micronuclei formation</title><author>Baliga, Manjeshwar S ; Diwadkar-Navsariwala, Veda ; Koh, Timothy ; Fayad, Raja ; Fantuzzi, Giamila ; Diamond, Alan M</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4050-d8a64e1841762fcc524ef72ac2dcb7fa9597344b072db73b4fc30e03dc2b83553</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2008</creationdate><topic>animal disease models</topic><topic>Animals</topic><topic>Base Sequence</topic><topic>chemoprevention</topic><topic>DNA Damage</topic><topic>erythrocytes</topic><topic>glutathione</topic><topic>Glutathione peroxidase</topic><topic>Glutathione Peroxidase - metabolism</topic><topic>Glutathione Peroxidase - radiation effects</topic><topic>humans</topic><topic>Mice</topic><topic>Mice, Transgenic</topic><topic>Micronucleus, Germline - drug effects</topic><topic>Micronucleus, Germline - radiation effects</topic><topic>neoplasms</topic><topic>nutrient availability</topic><topic>nutrient deficiencies</topic><topic>prostate gland</topic><topic>radiotherapy</topic><topic>risk</topic><topic>RNA, Messenger - genetics</topic><topic>RNA, Small Interfering - genetics</topic><topic>Selenium</topic><topic>Selenoproteins</topic><topic>Selenoproteins - deficiency</topic><topic>Selenoproteins - metabolism</topic><topic>Selenoproteins - radiation effects</topic><topic>small interfering RNA</topic><topic>transgenic animals</topic><topic>Ultraviolet Rays</topic><topic>X-radiation</topic><topic>X-Rays</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Baliga, Manjeshwar S</creatorcontrib><creatorcontrib>Diwadkar-Navsariwala, Veda</creatorcontrib><creatorcontrib>Koh, Timothy</creatorcontrib><creatorcontrib>Fayad, Raja</creatorcontrib><creatorcontrib>Fantuzzi, Giamila</creatorcontrib><creatorcontrib>Diamond, Alan M</creatorcontrib><collection>AGRIS</collection><collection>Istex</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Molecular nutrition & food research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Baliga, Manjeshwar S</au><au>Diwadkar-Navsariwala, Veda</au><au>Koh, Timothy</au><au>Fayad, Raja</au><au>Fantuzzi, Giamila</au><au>Diamond, Alan M</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Selenoprotein deficiency enhances radiation-induced micronuclei formation</atitle><jtitle>Molecular nutrition & food research</jtitle><addtitle>Mol. Nutr. Food Res</addtitle><date>2008-11</date><risdate>2008</risdate><volume>52</volume><issue>11</issue><spage>1300</spage><epage>1304</epage><pages>1300-1304</pages><issn>1613-4125</issn><eissn>1613-4133</eissn><abstract>The availability of selenium and the levels of specific selenoproteins might affect cancer risk by influencing the ability of DNA damaging agents to cause genomic instability and mutations. Transgenic mice that express reduced levels of selenoproteins and previously shown to be more susceptible to pathology associated with cancer development were used to study this possibility. These mice were exposed to X-rays and DNA damage assessed in the erythrocytes, where micronuclei formation was higher compared to the same cells obtained from irradiated wild-type controls. To determine whether the selenoprotein glutathione peroxidase-1 (GPx-1) might be involved in this protection, its levels were reduced by siRNA targeting in LNCaP human prostate cells. UV-induced micronuclei frequency was higher in these cells compared to control-transfected cells. These results indicate a role for selenoproteins in protecting DNA from damage and support human data implicating GPx-1 as a possible target of the chemoprotective effect of selenium.</abstract><cop>Weinheim</cop><pub>Wiley-VCH Verlag</pub><pmid>18720346</pmid><doi>10.1002/mnfr.200800020</doi><tpages>5</tpages></addata></record> |
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subjects | animal disease models Animals Base Sequence chemoprevention DNA Damage erythrocytes glutathione Glutathione peroxidase Glutathione Peroxidase - metabolism Glutathione Peroxidase - radiation effects humans Mice Mice, Transgenic Micronucleus, Germline - drug effects Micronucleus, Germline - radiation effects neoplasms nutrient availability nutrient deficiencies prostate gland radiotherapy risk RNA, Messenger - genetics RNA, Small Interfering - genetics Selenium Selenoproteins Selenoproteins - deficiency Selenoproteins - metabolism Selenoproteins - radiation effects small interfering RNA transgenic animals Ultraviolet Rays X-radiation X-Rays |
title | Selenoprotein deficiency enhances radiation-induced micronuclei formation |
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