Dinucleotide polymorphism of p73 gene is associated with a reduced risk of lung cancer in a Chinese population
p73, a structural and functional homologue of p53, shares some p53‐like tumor suppressor activity but also possesses oncogenic activity. Therefore, p73 plays an important role in modulating cell‐cycle control and apoptosis. A potentially functional dinucleotide polymorphism, G4C14‐to‐A4T14, has been...
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Veröffentlicht in: | International journal of cancer 2005-04, Vol.114 (3), p.455-460 |
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description | p73, a structural and functional homologue of p53, shares some p53‐like tumor suppressor activity but also possesses oncogenic activity. Therefore, p73 plays an important role in modulating cell‐cycle control and apoptosis. A potentially functional dinucleotide polymorphism, G4C14‐to‐A4T14, has been identified in the 5′ untranslated region (UTR) of exon 2 of the p73 gene, which may theoretically form a stem‐loop structure and affect gene expression. To test the hypothesis that these 2 common variants play a role in lung cancer susceptibility, we conducted a case‐control study of 425 lung cancer patients and 588 cancer‐free controls frequency‐matched to the cases on age and sex in a Chinese population. The results showed that these 2 polymorphisms were in complete linkage disequilibrium and the frequencies of variant p73 AT haplotype (A4T14) were less common in the cases (0.225) than in the controls (0.287) (p = 0.0018), suggesting that this AT haplotype was protective against lung cancer. Compared to the p73 GC/GC homozygotes, both the AT/AT variant homozygotes and GC/AT heterozygotes were associated with a significantly decreased risk (adjusted OR: 0.45, 95% CI: 0.26–0.80 and OR: 0.70, 95% CI: 0.53–0.92, respectively). These results suggest that this p73 dinucleotide polymorphism may have a role in lung cancer susceptibility in our study population. Further studies are needed to elucidate potential functional relevance of the p73 AT variant allele. © 2004 Wiley‐Liss, Inc. |
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Therefore, p73 plays an important role in modulating cell‐cycle control and apoptosis. A potentially functional dinucleotide polymorphism, G4C14‐to‐A4T14, has been identified in the 5′ untranslated region (UTR) of exon 2 of the p73 gene, which may theoretically form a stem‐loop structure and affect gene expression. To test the hypothesis that these 2 common variants play a role in lung cancer susceptibility, we conducted a case‐control study of 425 lung cancer patients and 588 cancer‐free controls frequency‐matched to the cases on age and sex in a Chinese population. The results showed that these 2 polymorphisms were in complete linkage disequilibrium and the frequencies of variant p73 AT haplotype (A4T14) were less common in the cases (0.225) than in the controls (0.287) (p = 0.0018), suggesting that this AT haplotype was protective against lung cancer. Compared to the p73 GC/GC homozygotes, both the AT/AT variant homozygotes and GC/AT heterozygotes were associated with a significantly decreased risk (adjusted OR: 0.45, 95% CI: 0.26–0.80 and OR: 0.70, 95% CI: 0.53–0.92, respectively). These results suggest that this p73 dinucleotide polymorphism may have a role in lung cancer susceptibility in our study population. Further studies are needed to elucidate potential functional relevance of the p73 AT variant allele. © 2004 Wiley‐Liss, Inc.</description><identifier>ISSN: 0020-7136</identifier><identifier>EISSN: 1097-0215</identifier><identifier>DOI: 10.1002/ijc.20746</identifier><identifier>PMID: 15578704</identifier><identifier>CODEN: IJCNAW</identifier><language>eng</language><publisher>Hoboken: Wiley Subscription Services, Inc., A Wiley Company</publisher><subject>Aged ; Base Sequence ; Biological and medical sciences ; Case-Control Studies ; China - epidemiology ; DNA-Binding Proteins - genetics ; Female ; Genes, Tumor Suppressor ; genetic susceptibility ; Humans ; Linkage Disequilibrium ; lung cancer ; Lung Neoplasms - epidemiology ; Lung Neoplasms - genetics ; Lung Neoplasms - prevention & control ; Male ; Medical sciences ; Middle Aged ; molecular epidemiology ; Molecular Sequence Data ; Nuclear Proteins - genetics ; Odds Ratio ; p73 ; Pneumology ; Polymorphism, Genetic ; polymorphisms ; Risk Factors ; Tropical medicine ; Tumor Protein p73 ; Tumor Suppressor Proteins ; Tumors ; Tumors of the respiratory system and mediastinum</subject><ispartof>International journal of cancer, 2005-04, Vol.114 (3), p.455-460</ispartof><rights>Copyright © 2004 Wiley‐Liss, Inc.</rights><rights>2005 INIST-CNRS</rights><rights>(c) 2004 Wiley-Liss, Inc.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4196-dbb9fd19b72847576ea7583828fdce2dfe65e4e43ea823c5376d7cea3d9341063</citedby><cites>FETCH-LOGICAL-c4196-dbb9fd19b72847576ea7583828fdce2dfe65e4e43ea823c5376d7cea3d9341063</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%2Fijc.20746$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fijc.20746$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,780,784,1416,27923,27924,45573,45574</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=16565196$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/15578704$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Hu, Zhibin</creatorcontrib><creatorcontrib>Miao, Xiaoping</creatorcontrib><creatorcontrib>Ma, Hongxia</creatorcontrib><creatorcontrib>Tan, Wen</creatorcontrib><creatorcontrib>Wang, Xinru</creatorcontrib><creatorcontrib>Lu, Daru</creatorcontrib><creatorcontrib>Wei, Qingyi</creatorcontrib><creatorcontrib>Lin, Dongxin</creatorcontrib><creatorcontrib>Shen, Hongbing</creatorcontrib><title>Dinucleotide polymorphism of p73 gene is associated with a reduced risk of lung cancer in a Chinese population</title><title>International journal of cancer</title><addtitle>Int J Cancer</addtitle><description>p73, a structural and functional homologue of p53, shares some p53‐like tumor suppressor activity but also possesses oncogenic activity. Therefore, p73 plays an important role in modulating cell‐cycle control and apoptosis. A potentially functional dinucleotide polymorphism, G4C14‐to‐A4T14, has been identified in the 5′ untranslated region (UTR) of exon 2 of the p73 gene, which may theoretically form a stem‐loop structure and affect gene expression. To test the hypothesis that these 2 common variants play a role in lung cancer susceptibility, we conducted a case‐control study of 425 lung cancer patients and 588 cancer‐free controls frequency‐matched to the cases on age and sex in a Chinese population. The results showed that these 2 polymorphisms were in complete linkage disequilibrium and the frequencies of variant p73 AT haplotype (A4T14) were less common in the cases (0.225) than in the controls (0.287) (p = 0.0018), suggesting that this AT haplotype was protective against lung cancer. Compared to the p73 GC/GC homozygotes, both the AT/AT variant homozygotes and GC/AT heterozygotes were associated with a significantly decreased risk (adjusted OR: 0.45, 95% CI: 0.26–0.80 and OR: 0.70, 95% CI: 0.53–0.92, respectively). These results suggest that this p73 dinucleotide polymorphism may have a role in lung cancer susceptibility in our study population. Further studies are needed to elucidate potential functional relevance of the p73 AT variant allele. © 2004 Wiley‐Liss, Inc.</description><subject>Aged</subject><subject>Base Sequence</subject><subject>Biological and medical sciences</subject><subject>Case-Control Studies</subject><subject>China - epidemiology</subject><subject>DNA-Binding Proteins - genetics</subject><subject>Female</subject><subject>Genes, Tumor Suppressor</subject><subject>genetic susceptibility</subject><subject>Humans</subject><subject>Linkage Disequilibrium</subject><subject>lung cancer</subject><subject>Lung Neoplasms - epidemiology</subject><subject>Lung Neoplasms - genetics</subject><subject>Lung Neoplasms - prevention & control</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>molecular epidemiology</subject><subject>Molecular Sequence Data</subject><subject>Nuclear Proteins - genetics</subject><subject>Odds Ratio</subject><subject>p73</subject><subject>Pneumology</subject><subject>Polymorphism, Genetic</subject><subject>polymorphisms</subject><subject>Risk Factors</subject><subject>Tropical medicine</subject><subject>Tumor Protein p73</subject><subject>Tumor Suppressor Proteins</subject><subject>Tumors</subject><subject>Tumors of the respiratory system and mediastinum</subject><issn>0020-7136</issn><issn>1097-0215</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2005</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqF0U9rFDEYBvAgFru2HvwCkouCh2nzPzNHWVtbKfSi5yGbvNNNzSRjMkPZb2-2u9CT9BRe8uN54X0Q-kjJBSWEXfpHe8GIFuoNWlHS6YYwKt-iVf0jjaZcnaL3pTwSQqkk4h06pVLqVhOxQvG7j4sNkGbvAE8p7MaUp60vI04DnjTHDxAB-4JNKcl6M4PDT37eYoMzuMXWMfvyZ6_DEh-wNdFCxj5WsN76CGUfOy3BzD7Fc3QymFDgw_E9Q7-vr36tb5q7-x-36293jRW0U43bbLrB0W6jWSu01AqMli1vWTs4C8wNoCQIEBxMy7iVXCunLRjuOi4oUfwMfTnkTjn9XaDM_eiLhRBMhLSUXmmxT34dUs2Z7DSr8OsB2pxKyTD0U_ajybuekn7fQl9b6J9bqPbTMXTZjOBe5PHsFXw-AlOsCUOuR_PlxSmpZL1DdZcH9-QD7P6_sb_9uT6s_gcMVZ4r</recordid><startdate>20050410</startdate><enddate>20050410</enddate><creator>Hu, Zhibin</creator><creator>Miao, Xiaoping</creator><creator>Ma, Hongxia</creator><creator>Tan, Wen</creator><creator>Wang, Xinru</creator><creator>Lu, Daru</creator><creator>Wei, Qingyi</creator><creator>Lin, Dongxin</creator><creator>Shen, Hongbing</creator><general>Wiley Subscription Services, Inc., A Wiley Company</general><general>Wiley-Liss</general><scope>IQODW</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>7TO</scope><scope>H94</scope><scope>7X8</scope></search><sort><creationdate>20050410</creationdate><title>Dinucleotide polymorphism of p73 gene is associated with a reduced risk of lung cancer in a Chinese population</title><author>Hu, Zhibin ; Miao, Xiaoping ; Ma, Hongxia ; Tan, Wen ; Wang, Xinru ; Lu, Daru ; Wei, Qingyi ; Lin, Dongxin ; Shen, Hongbing</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4196-dbb9fd19b72847576ea7583828fdce2dfe65e4e43ea823c5376d7cea3d9341063</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2005</creationdate><topic>Aged</topic><topic>Base Sequence</topic><topic>Biological and medical sciences</topic><topic>Case-Control Studies</topic><topic>China - epidemiology</topic><topic>DNA-Binding Proteins - genetics</topic><topic>Female</topic><topic>Genes, Tumor Suppressor</topic><topic>genetic susceptibility</topic><topic>Humans</topic><topic>Linkage Disequilibrium</topic><topic>lung cancer</topic><topic>Lung Neoplasms - epidemiology</topic><topic>Lung Neoplasms - genetics</topic><topic>Lung Neoplasms - prevention & control</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Middle Aged</topic><topic>molecular epidemiology</topic><topic>Molecular Sequence Data</topic><topic>Nuclear Proteins - genetics</topic><topic>Odds Ratio</topic><topic>p73</topic><topic>Pneumology</topic><topic>Polymorphism, Genetic</topic><topic>polymorphisms</topic><topic>Risk Factors</topic><topic>Tropical medicine</topic><topic>Tumor Protein p73</topic><topic>Tumor Suppressor Proteins</topic><topic>Tumors</topic><topic>Tumors of the respiratory system and mediastinum</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Hu, Zhibin</creatorcontrib><creatorcontrib>Miao, Xiaoping</creatorcontrib><creatorcontrib>Ma, Hongxia</creatorcontrib><creatorcontrib>Tan, Wen</creatorcontrib><creatorcontrib>Wang, Xinru</creatorcontrib><creatorcontrib>Lu, Daru</creatorcontrib><creatorcontrib>Wei, Qingyi</creatorcontrib><creatorcontrib>Lin, Dongxin</creatorcontrib><creatorcontrib>Shen, Hongbing</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Oncogenes and Growth Factors Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>International journal of cancer</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Hu, Zhibin</au><au>Miao, Xiaoping</au><au>Ma, Hongxia</au><au>Tan, Wen</au><au>Wang, Xinru</au><au>Lu, Daru</au><au>Wei, Qingyi</au><au>Lin, Dongxin</au><au>Shen, Hongbing</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Dinucleotide polymorphism of p73 gene is associated with a reduced risk of lung cancer in a Chinese population</atitle><jtitle>International journal of cancer</jtitle><addtitle>Int J Cancer</addtitle><date>2005-04-10</date><risdate>2005</risdate><volume>114</volume><issue>3</issue><spage>455</spage><epage>460</epage><pages>455-460</pages><issn>0020-7136</issn><eissn>1097-0215</eissn><coden>IJCNAW</coden><abstract>p73, a structural and functional homologue of p53, shares some p53‐like tumor suppressor activity but also possesses oncogenic activity. Therefore, p73 plays an important role in modulating cell‐cycle control and apoptosis. A potentially functional dinucleotide polymorphism, G4C14‐to‐A4T14, has been identified in the 5′ untranslated region (UTR) of exon 2 of the p73 gene, which may theoretically form a stem‐loop structure and affect gene expression. To test the hypothesis that these 2 common variants play a role in lung cancer susceptibility, we conducted a case‐control study of 425 lung cancer patients and 588 cancer‐free controls frequency‐matched to the cases on age and sex in a Chinese population. The results showed that these 2 polymorphisms were in complete linkage disequilibrium and the frequencies of variant p73 AT haplotype (A4T14) were less common in the cases (0.225) than in the controls (0.287) (p = 0.0018), suggesting that this AT haplotype was protective against lung cancer. Compared to the p73 GC/GC homozygotes, both the AT/AT variant homozygotes and GC/AT heterozygotes were associated with a significantly decreased risk (adjusted OR: 0.45, 95% CI: 0.26–0.80 and OR: 0.70, 95% CI: 0.53–0.92, respectively). These results suggest that this p73 dinucleotide polymorphism may have a role in lung cancer susceptibility in our study population. Further studies are needed to elucidate potential functional relevance of the p73 AT variant allele. © 2004 Wiley‐Liss, Inc.</abstract><cop>Hoboken</cop><pub>Wiley Subscription Services, Inc., A Wiley Company</pub><pmid>15578704</pmid><doi>10.1002/ijc.20746</doi><tpages>6</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Aged Base Sequence Biological and medical sciences Case-Control Studies China - epidemiology DNA-Binding Proteins - genetics Female Genes, Tumor Suppressor genetic susceptibility Humans Linkage Disequilibrium lung cancer Lung Neoplasms - epidemiology Lung Neoplasms - genetics Lung Neoplasms - prevention & control Male Medical sciences Middle Aged molecular epidemiology Molecular Sequence Data Nuclear Proteins - genetics Odds Ratio p73 Pneumology Polymorphism, Genetic polymorphisms Risk Factors Tropical medicine Tumor Protein p73 Tumor Suppressor Proteins Tumors Tumors of the respiratory system and mediastinum |
title | Dinucleotide polymorphism of p73 gene is associated with a reduced risk of lung cancer in a Chinese population |
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