Association of p53 mutations and a codon 72 single nucleotide polymorphism with lower overall survival and responsiveness to adjuvant radiotherapy in endometrioid endometrial carcinomas
. Saffari B, Bernstein L, Hong DC, Sullivan‐Halley J, Runnebaum IB, Grill H‐J, Jones LA, El‐Naggar A, Press MF. Association of p53 mutations and a codon 72 single nucleotide polymorphism with lower overall survival and responsiveness to adjuvant radiotherapy in endometrioid endometrial carcinomas....
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creator | SAFFARI, B. BERNSTEIN, L. HONG, D.C. SULLIVAN‐HALLEY, J. RUNNEBAUM, I.B. GRILL, H.‐J. JONES, L.A. EL‐NAGGAR, A. PRESS, M.F. |
description | . Saffari B, Bernstein L, Hong DC, Sullivan‐Halley J, Runnebaum IB, Grill H‐J, Jones LA, El‐Naggar A, Press MF. Association of p53 mutations and a codon 72 single nucleotide polymorphism with lower overall survival and responsiveness to adjuvant radiotherapy in endometrioid endometrial carcinomas. Int J Gynecol Cancer 2005;15:952–963.
p53 genetic alterations are associated with advanced stage and aggressive tumors in a variety of human malignancies. The aim of this study was to examine p53 for genetic alterations and to evaluate the association of these alterations with clinical outcome and response to adjuvant radiotherapy in endometrioid endometrial carcinomas. p53 mutations in exons 2–11 were assessed in 59 endometrioid carcinomas by polymerase chain reaction–single‐strand conformational polymorphism and sequence analysis. Twelve mutations (20.3%) and nine polymorphisms were identified. Seven of the nine polymorphisms were codon 72 single nucleotide polymorphisms (SNP) with an Arg/Pro allelotype. Women harboring either a mutation or an Arg/Pro allelotype at codon 72 had a lower overall survival rate than women whose tumors lacked alterations in the p53 gene (P= 0.0029). Women were stratified based on p53 genetic alterations (p53 mutation or p53 codon 72 SNP) and whether or not they received adjuvant radiation therapy. Women with p53 genetic alterations who did not receive adjuvant radiotherapy had the lowest survival rate (P= 0.0005). Treated women with p53 genetic alterations and untreated women with no p53 alteration had similar rates of survival. Among women with p53 alterations, adjuvant radiotherapy substantially increased survival (P= 0.035). In multivariate analyses, the group of women with p53 genetic alterations who did not receive adjuvant radiation therapy had a 5.9‐fold increased risk of death (95% confidence interval: 1.5–22.7) compared to women whose tumors lacked p53 alterations and did not receive adjuvant radiation therapy. |
doi_str_mv | 10.1111/j.1525-1438.2005.00159.x |
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p53 genetic alterations are associated with advanced stage and aggressive tumors in a variety of human malignancies. The aim of this study was to examine p53 for genetic alterations and to evaluate the association of these alterations with clinical outcome and response to adjuvant radiotherapy in endometrioid endometrial carcinomas. p53 mutations in exons 2–11 were assessed in 59 endometrioid carcinomas by polymerase chain reaction–single‐strand conformational polymorphism and sequence analysis. Twelve mutations (20.3%) and nine polymorphisms were identified. Seven of the nine polymorphisms were codon 72 single nucleotide polymorphisms (SNP) with an Arg/Pro allelotype. Women harboring either a mutation or an Arg/Pro allelotype at codon 72 had a lower overall survival rate than women whose tumors lacked alterations in the p53 gene (P= 0.0029). Women were stratified based on p53 genetic alterations (p53 mutation or p53 codon 72 SNP) and whether or not they received adjuvant radiation therapy. Women with p53 genetic alterations who did not receive adjuvant radiotherapy had the lowest survival rate (P= 0.0005). Treated women with p53 genetic alterations and untreated women with no p53 alteration had similar rates of survival. Among women with p53 alterations, adjuvant radiotherapy substantially increased survival (P= 0.035). In multivariate analyses, the group of women with p53 genetic alterations who did not receive adjuvant radiation therapy had a 5.9‐fold increased risk of death (95% confidence interval: 1.5–22.7) compared to women whose tumors lacked p53 alterations and did not receive adjuvant radiation therapy.</description><identifier>ISSN: 1048-891X</identifier><identifier>EISSN: 1525-1438</identifier><identifier>DOI: 10.1111/j.1525-1438.2005.00159.x</identifier><identifier>PMID: 16174251</identifier><language>eng</language><publisher>Oxford, UK; Malden, USA: Blackwell Science Inc</publisher><subject>adjuvant radiation therapy and prognosis ; Adult ; Aged ; Aged, 80 and over ; Base Sequence ; Biomarkers, Tumor ; Carcinoma, Endometrioid - genetics ; Carcinoma, Endometrioid - pathology ; Carcinoma, Endometrioid - radiotherapy ; Codon - genetics ; DNA sequence analysis ; Endometrial Neoplasms - genetics ; Endometrial Neoplasms - pathology ; Endometrial Neoplasms - radiotherapy ; endometrioid‐type endometrial carcinomas ; Exons - genetics ; Female ; Germ Cells - metabolism ; Humans ; Middle Aged ; p53 ; Polymorphism, Single Nucleotide - genetics ; Prognosis ; Radiotherapy, Adjuvant ; Retrospective Studies ; Survival Rate ; Tumor Suppressor Protein p53 - genetics</subject><ispartof>International journal of gynecological cancer, 2005-09, Vol.15 (5), p.952-963</ispartof><rights>Copyright © 2005 Blackwell Publishing Ltd.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4428-3c0a3d011a6badce0524d6692daeb39abaf9fa3da0964625ac7492fa0732560a3</citedby><cites>FETCH-LOGICAL-c4428-3c0a3d011a6badce0524d6692daeb39abaf9fa3da0964625ac7492fa0732560a3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1111%2Fj.1525-1438.2005.00159.x$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2Fj.1525-1438.2005.00159.x$$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/16174251$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>SAFFARI, B.</creatorcontrib><creatorcontrib>BERNSTEIN, L.</creatorcontrib><creatorcontrib>HONG, D.C.</creatorcontrib><creatorcontrib>SULLIVAN‐HALLEY, J.</creatorcontrib><creatorcontrib>RUNNEBAUM, I.B.</creatorcontrib><creatorcontrib>GRILL, H.‐J.</creatorcontrib><creatorcontrib>JONES, L.A.</creatorcontrib><creatorcontrib>EL‐NAGGAR, A.</creatorcontrib><creatorcontrib>PRESS, M.F.</creatorcontrib><title>Association of p53 mutations and a codon 72 single nucleotide polymorphism with lower overall survival and responsiveness to adjuvant radiotherapy in endometrioid endometrial carcinomas</title><title>International journal of gynecological cancer</title><addtitle>Int J Gynecol Cancer</addtitle><description>. Saffari B, Bernstein L, Hong DC, Sullivan‐Halley J, Runnebaum IB, Grill H‐J, Jones LA, El‐Naggar A, Press MF. Association of p53 mutations and a codon 72 single nucleotide polymorphism with lower overall survival and responsiveness to adjuvant radiotherapy in endometrioid endometrial carcinomas. Int J Gynecol Cancer 2005;15:952–963.
p53 genetic alterations are associated with advanced stage and aggressive tumors in a variety of human malignancies. The aim of this study was to examine p53 for genetic alterations and to evaluate the association of these alterations with clinical outcome and response to adjuvant radiotherapy in endometrioid endometrial carcinomas. p53 mutations in exons 2–11 were assessed in 59 endometrioid carcinomas by polymerase chain reaction–single‐strand conformational polymorphism and sequence analysis. Twelve mutations (20.3%) and nine polymorphisms were identified. Seven of the nine polymorphisms were codon 72 single nucleotide polymorphisms (SNP) with an Arg/Pro allelotype. Women harboring either a mutation or an Arg/Pro allelotype at codon 72 had a lower overall survival rate than women whose tumors lacked alterations in the p53 gene (P= 0.0029). Women were stratified based on p53 genetic alterations (p53 mutation or p53 codon 72 SNP) and whether or not they received adjuvant radiation therapy. Women with p53 genetic alterations who did not receive adjuvant radiotherapy had the lowest survival rate (P= 0.0005). Treated women with p53 genetic alterations and untreated women with no p53 alteration had similar rates of survival. Among women with p53 alterations, adjuvant radiotherapy substantially increased survival (P= 0.035). In multivariate analyses, the group of women with p53 genetic alterations who did not receive adjuvant radiation therapy had a 5.9‐fold increased risk of death (95% confidence interval: 1.5–22.7) compared to women whose tumors lacked p53 alterations and did not receive adjuvant radiation therapy.</description><subject>adjuvant radiation therapy and prognosis</subject><subject>Adult</subject><subject>Aged</subject><subject>Aged, 80 and over</subject><subject>Base Sequence</subject><subject>Biomarkers, Tumor</subject><subject>Carcinoma, Endometrioid - genetics</subject><subject>Carcinoma, Endometrioid - pathology</subject><subject>Carcinoma, Endometrioid - radiotherapy</subject><subject>Codon - genetics</subject><subject>DNA sequence analysis</subject><subject>Endometrial Neoplasms - genetics</subject><subject>Endometrial Neoplasms - pathology</subject><subject>Endometrial Neoplasms - radiotherapy</subject><subject>endometrioid‐type endometrial carcinomas</subject><subject>Exons - genetics</subject><subject>Female</subject><subject>Germ Cells - metabolism</subject><subject>Humans</subject><subject>Middle Aged</subject><subject>p53</subject><subject>Polymorphism, Single Nucleotide - genetics</subject><subject>Prognosis</subject><subject>Radiotherapy, Adjuvant</subject><subject>Retrospective Studies</subject><subject>Survival Rate</subject><subject>Tumor Suppressor Protein p53 - genetics</subject><issn>1048-891X</issn><issn>1525-1438</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2005</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNksFu1DAQhiMEoqXwCsgnbllsJ3FiiUtV0VJUiQtI3KxZe8J6ceJgO7vdR-PtcHZX9AiWLM9o_v-3pc9FQRhdsbzeb1es4U3J6qpbcUqbFaWskavHZ8Xl38HzXNO6KzvJvl8Ur2LcUkolp_JlccEEa2vesMvi93WMXltI1o_E92RqKjLM6dhHAqMhQLQ3edhyEu34wyEZZ-3QJ2uQTN4dBh-mjY0D2du0Ic7vMRC_wwDOkTiHnd2BOyYFjFNOtTscMUaSPAGznXcwJhLAWJ822TQdiB0JjsYPmIL11jw1OUdD0Hb0A8TXxYseXMQ35_Oq-Hb78evNp_Lhy939zfVDqeuad2WlKVSGMgZiDUYjbXhthJDcAK4rCWvoZZ8VQKWoBW9At7XkPdC24o3I3qvi3Sl3Cv7XjDGpwUaNzsGIfo5KdIIK1vF_CpmsOedCZGF3EurgYwzYqynYAcJBMaoWvmqrFoxqwagWvurIVz1m69vzHfN6QPNkPAPNgvok2HuXMMSfbs481AbBpU2OyV-gadtyCaUyd2XeVZdtH8426_Dw3-9R95_vclH9AWYMyRU</recordid><startdate>200509</startdate><enddate>200509</enddate><creator>SAFFARI, B.</creator><creator>BERNSTEIN, L.</creator><creator>HONG, D.C.</creator><creator>SULLIVAN‐HALLEY, J.</creator><creator>RUNNEBAUM, I.B.</creator><creator>GRILL, H.‐J.</creator><creator>JONES, L.A.</creator><creator>EL‐NAGGAR, A.</creator><creator>PRESS, M.F.</creator><general>Blackwell Science Inc</general><general>Copyright Blackwell Publishing Ltd</general><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>7TM</scope><scope>7TO</scope><scope>8FD</scope><scope>FR3</scope><scope>H94</scope><scope>P64</scope><scope>RC3</scope><scope>7X8</scope></search><sort><creationdate>200509</creationdate><title>Association of p53 mutations and a codon 72 single nucleotide polymorphism with lower overall survival and responsiveness to adjuvant radiotherapy in endometrioid endometrial carcinomas</title><author>SAFFARI, B. ; BERNSTEIN, L. ; HONG, D.C. ; SULLIVAN‐HALLEY, J. ; RUNNEBAUM, I.B. ; GRILL, H.‐J. ; JONES, L.A. ; EL‐NAGGAR, A. ; PRESS, M.F.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4428-3c0a3d011a6badce0524d6692daeb39abaf9fa3da0964625ac7492fa0732560a3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2005</creationdate><topic>adjuvant radiation therapy and prognosis</topic><topic>Adult</topic><topic>Aged</topic><topic>Aged, 80 and over</topic><topic>Base Sequence</topic><topic>Biomarkers, Tumor</topic><topic>Carcinoma, Endometrioid - genetics</topic><topic>Carcinoma, Endometrioid - pathology</topic><topic>Carcinoma, Endometrioid - radiotherapy</topic><topic>Codon - genetics</topic><topic>DNA sequence analysis</topic><topic>Endometrial Neoplasms - genetics</topic><topic>Endometrial Neoplasms - pathology</topic><topic>Endometrial Neoplasms - radiotherapy</topic><topic>endometrioid‐type endometrial carcinomas</topic><topic>Exons - genetics</topic><topic>Female</topic><topic>Germ Cells - metabolism</topic><topic>Humans</topic><topic>Middle Aged</topic><topic>p53</topic><topic>Polymorphism, Single Nucleotide - genetics</topic><topic>Prognosis</topic><topic>Radiotherapy, Adjuvant</topic><topic>Retrospective Studies</topic><topic>Survival Rate</topic><topic>Tumor Suppressor Protein p53 - genetics</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>SAFFARI, B.</creatorcontrib><creatorcontrib>BERNSTEIN, L.</creatorcontrib><creatorcontrib>HONG, D.C.</creatorcontrib><creatorcontrib>SULLIVAN‐HALLEY, J.</creatorcontrib><creatorcontrib>RUNNEBAUM, I.B.</creatorcontrib><creatorcontrib>GRILL, H.‐J.</creatorcontrib><creatorcontrib>JONES, L.A.</creatorcontrib><creatorcontrib>EL‐NAGGAR, A.</creatorcontrib><creatorcontrib>PRESS, M.F.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Nucleic Acids Abstracts</collection><collection>Oncogenes and Growth Factors Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>International journal of gynecological cancer</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>SAFFARI, B.</au><au>BERNSTEIN, L.</au><au>HONG, D.C.</au><au>SULLIVAN‐HALLEY, J.</au><au>RUNNEBAUM, I.B.</au><au>GRILL, H.‐J.</au><au>JONES, L.A.</au><au>EL‐NAGGAR, A.</au><au>PRESS, M.F.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Association of p53 mutations and a codon 72 single nucleotide polymorphism with lower overall survival and responsiveness to adjuvant radiotherapy in endometrioid endometrial carcinomas</atitle><jtitle>International journal of gynecological cancer</jtitle><addtitle>Int J Gynecol Cancer</addtitle><date>2005-09</date><risdate>2005</risdate><volume>15</volume><issue>5</issue><spage>952</spage><epage>963</epage><pages>952-963</pages><issn>1048-891X</issn><eissn>1525-1438</eissn><abstract>. Saffari B, Bernstein L, Hong DC, Sullivan‐Halley J, Runnebaum IB, Grill H‐J, Jones LA, El‐Naggar A, Press MF. Association of p53 mutations and a codon 72 single nucleotide polymorphism with lower overall survival and responsiveness to adjuvant radiotherapy in endometrioid endometrial carcinomas. Int J Gynecol Cancer 2005;15:952–963.
p53 genetic alterations are associated with advanced stage and aggressive tumors in a variety of human malignancies. The aim of this study was to examine p53 for genetic alterations and to evaluate the association of these alterations with clinical outcome and response to adjuvant radiotherapy in endometrioid endometrial carcinomas. p53 mutations in exons 2–11 were assessed in 59 endometrioid carcinomas by polymerase chain reaction–single‐strand conformational polymorphism and sequence analysis. Twelve mutations (20.3%) and nine polymorphisms were identified. Seven of the nine polymorphisms were codon 72 single nucleotide polymorphisms (SNP) with an Arg/Pro allelotype. Women harboring either a mutation or an Arg/Pro allelotype at codon 72 had a lower overall survival rate than women whose tumors lacked alterations in the p53 gene (P= 0.0029). Women were stratified based on p53 genetic alterations (p53 mutation or p53 codon 72 SNP) and whether or not they received adjuvant radiation therapy. Women with p53 genetic alterations who did not receive adjuvant radiotherapy had the lowest survival rate (P= 0.0005). Treated women with p53 genetic alterations and untreated women with no p53 alteration had similar rates of survival. Among women with p53 alterations, adjuvant radiotherapy substantially increased survival (P= 0.035). In multivariate analyses, the group of women with p53 genetic alterations who did not receive adjuvant radiation therapy had a 5.9‐fold increased risk of death (95% confidence interval: 1.5–22.7) compared to women whose tumors lacked p53 alterations and did not receive adjuvant radiation therapy.</abstract><cop>Oxford, UK; Malden, USA</cop><pub>Blackwell Science Inc</pub><pmid>16174251</pmid><doi>10.1111/j.1525-1438.2005.00159.x</doi><tpages>12</tpages></addata></record> |
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subjects | adjuvant radiation therapy and prognosis Adult Aged Aged, 80 and over Base Sequence Biomarkers, Tumor Carcinoma, Endometrioid - genetics Carcinoma, Endometrioid - pathology Carcinoma, Endometrioid - radiotherapy Codon - genetics DNA sequence analysis Endometrial Neoplasms - genetics Endometrial Neoplasms - pathology Endometrial Neoplasms - radiotherapy endometrioid‐type endometrial carcinomas Exons - genetics Female Germ Cells - metabolism Humans Middle Aged p53 Polymorphism, Single Nucleotide - genetics Prognosis Radiotherapy, Adjuvant Retrospective Studies Survival Rate Tumor Suppressor Protein p53 - genetics |
title | Association of p53 mutations and a codon 72 single nucleotide polymorphism with lower overall survival and responsiveness to adjuvant radiotherapy in endometrioid endometrial carcinomas |
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