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GSTM1, GSTT1 and GSTP1 gene polymorphism in polymorphous light eruption
Background Polymorphous light eruption (PLE) is the most common chronic and idiopathic photodermatosis. PLE is assumed to represent an immunological hypersensitivity reaction to a radiation‐induced cutaneous antigen involving reactive oxygen species (ROS) on the basis of a genetic predisposition. A...
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Published in: | Journal of the European Academy of Dermatology and Venereology 2013-02, Vol.27 (2), p.157-162 |
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description | Background Polymorphous light eruption (PLE) is the most common chronic and idiopathic photodermatosis. PLE is assumed to represent an immunological hypersensitivity reaction to a radiation‐induced cutaneous antigen involving reactive oxygen species (ROS) on the basis of a genetic predisposition. Among others, cellular protection against ROS is provided by glutathione S‐transferases (GSTs). Different variants of the GST enzymes may influence the activity and efficiency of detoxification and biotransformation of unknown UV‐induced skin‐antigens and other factors that may play an important role in the pathogenesis of PLE.
Methods In this study the relationship between isoenzymes of the GST genes GSTM1, GSTT1 and GSTP1 and possible protective or predisposing effects on PLE was examined in 29 patients and 144 controls. Diagnosis of PLE was based on the presence of characteristic clinical features.
Results No association between the functional polymorphisms of the GST gene family and PLE was found. Prevalence of certain GST isoenzymes or polymorphisms in patients with PLE did not differ from healthy controls.
Conclusion Our data do not support prevalence of GST isoenzymes or polymorphisms as a protective effect against PLE. Especially a higher carrier frequency of GSTP1 Val105 as a protective factor against PLE which has been published before could not be proved. The GST genotypes GSTM1, GSTT1 and GSTP1 (including SNPs) seem to have no relevant association with PLE. |
doi_str_mv | 10.1111/j.1468-3083.2011.04431.x |
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Methods In this study the relationship between isoenzymes of the GST genes GSTM1, GSTT1 and GSTP1 and possible protective or predisposing effects on PLE was examined in 29 patients and 144 controls. Diagnosis of PLE was based on the presence of characteristic clinical features.
Results No association between the functional polymorphisms of the GST gene family and PLE was found. Prevalence of certain GST isoenzymes or polymorphisms in patients with PLE did not differ from healthy controls.
Conclusion Our data do not support prevalence of GST isoenzymes or polymorphisms as a protective effect against PLE. Especially a higher carrier frequency of GSTP1 Val105 as a protective factor against PLE which has been published before could not be proved. The GST genotypes GSTM1, GSTT1 and GSTP1 (including SNPs) seem to have no relevant association with PLE.</description><identifier>ISSN: 0926-9959</identifier><identifier>EISSN: 1468-3083</identifier><identifier>DOI: 10.1111/j.1468-3083.2011.04431.x</identifier><identifier>PMID: 22225519</identifier><language>eng</language><publisher>Oxford, UK: Blackwell Publishing Ltd</publisher><subject>Adult ; Aged ; Aged, 80 and over ; Base Sequence ; DNA Primers ; Female ; Glutathione S-Transferase pi - genetics ; Glutathione Transferase - genetics ; Humans ; Male ; Middle Aged ; Photosensitivity Disorders - enzymology ; Photosensitivity Disorders - genetics ; Young Adult</subject><ispartof>Journal of the European Academy of Dermatology and Venereology, 2013-02, Vol.27 (2), p.157-162</ispartof><rights>2012 The Authors. Journal of the European Academy of Dermatology and Venereology © 2012 European Academy of Dermatology and Venereology</rights><rights>2012 The Authors. Journal of the European Academy of Dermatology and Venereology © 2012 European Academy of Dermatology and Venereology.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4571-1991761c2a3b8ee11a1248cf9e310418c9d8a44fbf3a5cbbe8997c43de95a7d83</citedby><cites>FETCH-LOGICAL-c4571-1991761c2a3b8ee11a1248cf9e310418c9d8a44fbf3a5cbbe8997c43de95a7d83</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/22225519$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Zirbs, M.</creatorcontrib><creatorcontrib>Pürner, C.</creatorcontrib><creatorcontrib>Buters, J.T.M.</creatorcontrib><creatorcontrib>Effner, R.</creatorcontrib><creatorcontrib>Weidinger, S.</creatorcontrib><creatorcontrib>Ring, J.</creatorcontrib><creatorcontrib>Eberlein, B.</creatorcontrib><title>GSTM1, GSTT1 and GSTP1 gene polymorphism in polymorphous light eruption</title><title>Journal of the European Academy of Dermatology and Venereology</title><addtitle>J Eur Acad Dermatol Venereol</addtitle><description>Background Polymorphous light eruption (PLE) is the most common chronic and idiopathic photodermatosis. PLE is assumed to represent an immunological hypersensitivity reaction to a radiation‐induced cutaneous antigen involving reactive oxygen species (ROS) on the basis of a genetic predisposition. Among others, cellular protection against ROS is provided by glutathione S‐transferases (GSTs). Different variants of the GST enzymes may influence the activity and efficiency of detoxification and biotransformation of unknown UV‐induced skin‐antigens and other factors that may play an important role in the pathogenesis of PLE.
Methods In this study the relationship between isoenzymes of the GST genes GSTM1, GSTT1 and GSTP1 and possible protective or predisposing effects on PLE was examined in 29 patients and 144 controls. Diagnosis of PLE was based on the presence of characteristic clinical features.
Results No association between the functional polymorphisms of the GST gene family and PLE was found. Prevalence of certain GST isoenzymes or polymorphisms in patients with PLE did not differ from healthy controls.
Conclusion Our data do not support prevalence of GST isoenzymes or polymorphisms as a protective effect against PLE. Especially a higher carrier frequency of GSTP1 Val105 as a protective factor against PLE which has been published before could not be proved. The GST genotypes GSTM1, GSTT1 and GSTP1 (including SNPs) seem to have no relevant association with PLE.</description><subject>Adult</subject><subject>Aged</subject><subject>Aged, 80 and over</subject><subject>Base Sequence</subject><subject>DNA Primers</subject><subject>Female</subject><subject>Glutathione S-Transferase pi - genetics</subject><subject>Glutathione Transferase - genetics</subject><subject>Humans</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Photosensitivity Disorders - enzymology</subject><subject>Photosensitivity Disorders - genetics</subject><subject>Young Adult</subject><issn>0926-9959</issn><issn>1468-3083</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</creationdate><recordtype>article</recordtype><recordid>eNqNkE1PwzAMhiMEYmPwF1CPHGiJm6RNDhwQHwM0BhoDJC5R2qZbR79oNrH9e1I2xhVf7Mjva8cPQg5gD2yczTygAXcJ5sTzMYCHKSXgLXdQd9vYRV0s_MAVgokOOjBmhrGVMr6POr4NxkB0Ub__PH6AU8emMTiqTNrqCZyJLrVTV_mqqJp6mpnCycq_d7UwTp5NpnNHN4t6nlXlIdpLVW700Sb30MvN9fjy1h089u8uLwZuTFkILggBYQCxr0jEtQZQ4FMep0ITwBR4LBKuKE2jlCgWR5HmQoQxJYkWTIUJJz10sp5bN9XnQpu5LDIT6zxXpba_kuCHJAxDHggr5Wtp3FTGNDqVdZMVqllJwLLFKGeypSVbWrLFKH8wyqW1Hm-2LKJCJ1vjLzcrOF8LvrJcr_49WN5fvbaV9btrf2bmern1q-ZDBvYAJt-Gffk-8tmIwVAS8g0lyo4M</recordid><startdate>201302</startdate><enddate>201302</enddate><creator>Zirbs, M.</creator><creator>Pürner, C.</creator><creator>Buters, J.T.M.</creator><creator>Effner, R.</creator><creator>Weidinger, S.</creator><creator>Ring, J.</creator><creator>Eberlein, B.</creator><general>Blackwell Publishing Ltd</general><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>201302</creationdate><title>GSTM1, GSTT1 and GSTP1 gene polymorphism in polymorphous light eruption</title><author>Zirbs, M. ; Pürner, C. ; Buters, J.T.M. ; Effner, R. ; Weidinger, S. ; Ring, J. ; Eberlein, B.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4571-1991761c2a3b8ee11a1248cf9e310418c9d8a44fbf3a5cbbe8997c43de95a7d83</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2013</creationdate><topic>Adult</topic><topic>Aged</topic><topic>Aged, 80 and over</topic><topic>Base Sequence</topic><topic>DNA Primers</topic><topic>Female</topic><topic>Glutathione S-Transferase pi - genetics</topic><topic>Glutathione Transferase - genetics</topic><topic>Humans</topic><topic>Male</topic><topic>Middle Aged</topic><topic>Photosensitivity Disorders - enzymology</topic><topic>Photosensitivity Disorders - genetics</topic><topic>Young Adult</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Zirbs, M.</creatorcontrib><creatorcontrib>Pürner, C.</creatorcontrib><creatorcontrib>Buters, J.T.M.</creatorcontrib><creatorcontrib>Effner, R.</creatorcontrib><creatorcontrib>Weidinger, S.</creatorcontrib><creatorcontrib>Ring, J.</creatorcontrib><creatorcontrib>Eberlein, B.</creatorcontrib><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>Journal of the European Academy of Dermatology and Venereology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Zirbs, M.</au><au>Pürner, C.</au><au>Buters, J.T.M.</au><au>Effner, R.</au><au>Weidinger, S.</au><au>Ring, J.</au><au>Eberlein, B.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>GSTM1, GSTT1 and GSTP1 gene polymorphism in polymorphous light eruption</atitle><jtitle>Journal of the European Academy of Dermatology and Venereology</jtitle><addtitle>J Eur Acad Dermatol Venereol</addtitle><date>2013-02</date><risdate>2013</risdate><volume>27</volume><issue>2</issue><spage>157</spage><epage>162</epage><pages>157-162</pages><issn>0926-9959</issn><eissn>1468-3083</eissn><abstract>Background Polymorphous light eruption (PLE) is the most common chronic and idiopathic photodermatosis. PLE is assumed to represent an immunological hypersensitivity reaction to a radiation‐induced cutaneous antigen involving reactive oxygen species (ROS) on the basis of a genetic predisposition. Among others, cellular protection against ROS is provided by glutathione S‐transferases (GSTs). Different variants of the GST enzymes may influence the activity and efficiency of detoxification and biotransformation of unknown UV‐induced skin‐antigens and other factors that may play an important role in the pathogenesis of PLE.
Methods In this study the relationship between isoenzymes of the GST genes GSTM1, GSTT1 and GSTP1 and possible protective or predisposing effects on PLE was examined in 29 patients and 144 controls. Diagnosis of PLE was based on the presence of characteristic clinical features.
Results No association between the functional polymorphisms of the GST gene family and PLE was found. Prevalence of certain GST isoenzymes or polymorphisms in patients with PLE did not differ from healthy controls.
Conclusion Our data do not support prevalence of GST isoenzymes or polymorphisms as a protective effect against PLE. Especially a higher carrier frequency of GSTP1 Val105 as a protective factor against PLE which has been published before could not be proved. The GST genotypes GSTM1, GSTT1 and GSTP1 (including SNPs) seem to have no relevant association with PLE.</abstract><cop>Oxford, UK</cop><pub>Blackwell Publishing Ltd</pub><pmid>22225519</pmid><doi>10.1111/j.1468-3083.2011.04431.x</doi><tpages>6</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Adult Aged Aged, 80 and over Base Sequence DNA Primers Female Glutathione S-Transferase pi - genetics Glutathione Transferase - genetics Humans Male Middle Aged Photosensitivity Disorders - enzymology Photosensitivity Disorders - genetics Young Adult |
title | GSTM1, GSTT1 and GSTP1 gene polymorphism in polymorphous light eruption |
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