Lack of Association between EBV and Breast Carcinoma
Multiple conflicting findings have been presented which indicate that EBV may be found in anywhere from 0% to 51% of breast carcinomas. When EBV has been found causally associated with other human cancers, its DNA and one or more of its viral products have been detected in most tumor cells of a give...
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Veröffentlicht in: | Cancer epidemiology, biomarkers & prevention biomarkers & prevention, 2005-04, Vol.14 (4), p.809-814 |
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creator | PERRIGOUE, Jacqueline G DEN BOON, Johan A FRIEDL, Andreas NEWTON, Michael A AHLQUIST, Paul SUGDEN, Bill |
description | Multiple conflicting findings have been presented which indicate that EBV may be found in anywhere from 0% to 51% of breast
carcinomas. When EBV has been found causally associated with other human cancers, its DNA and one or more of its viral products
have been detected in most tumor cells of a given biopsy. To test whether EBV has such an association with breast cancer,
we measured the number of viral DNA molecules per cell in matched normal and tumor biopsies from 45 patients using real-time
quantitative PCR. In no case could EBV DNA consistently be detected, with either of two different probes, at levels above
0.1 molecules per cell in two sections of the tumor samples. These levels of detection match those detected in EBV-negative
cell lines and therefore likely represent noise in the assays. Equally importantly, the distribution of these low signals
was the same between tumors and their matched normal controls. We conclude that EBV does not contribute to the development
of breast cancers as it does to epithelial cancers such as nasopharyngeal and gastric carcinomas or to Burkitt's and Hodgkin's
lymphomas. |
doi_str_mv | 10.1158/1055-9965.EPI-04-0763 |
format | Article |
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carcinomas. When EBV has been found causally associated with other human cancers, its DNA and one or more of its viral products
have been detected in most tumor cells of a given biopsy. To test whether EBV has such an association with breast cancer,
we measured the number of viral DNA molecules per cell in matched normal and tumor biopsies from 45 patients using real-time
quantitative PCR. In no case could EBV DNA consistently be detected, with either of two different probes, at levels above
0.1 molecules per cell in two sections of the tumor samples. These levels of detection match those detected in EBV-negative
cell lines and therefore likely represent noise in the assays. Equally importantly, the distribution of these low signals
was the same between tumors and their matched normal controls. We conclude that EBV does not contribute to the development
of breast cancers as it does to epithelial cancers such as nasopharyngeal and gastric carcinomas or to Burkitt's and Hodgkin's
lymphomas.</description><identifier>ISSN: 1055-9965</identifier><identifier>EISSN: 1538-7755</identifier><identifier>DOI: 10.1158/1055-9965.EPI-04-0763</identifier><identifier>PMID: 15824148</identifier><language>eng</language><publisher>Philadelphia, PA: American Association for Cancer Research</publisher><subject>Actins - genetics ; Adult ; Aged ; Aged, 80 and over ; Biological and medical sciences ; breast cancer ; Breast Neoplasms - classification ; Breast Neoplasms - pathology ; Breast Neoplasms - virology ; Case-Control Studies ; DNA, Viral - isolation & purification ; EBV ; etiology ; Female ; Gynecology. Andrology. Obstetrics ; Herpesvirus 4, Human - isolation & purification ; Humans ; In Situ Hybridization - methods ; Mammary gland diseases ; Medical sciences ; Middle Aged ; real-time PCR ; Reverse Transcriptase Polymerase Chain Reaction ; Tumors</subject><ispartof>Cancer epidemiology, biomarkers & prevention, 2005-04, Vol.14 (4), p.809-814</ispartof><rights>2005 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c466t-afb2a81187d1585f5db0185d76dc0b074cb027f2dfd5c354a1036f5b0c8f24c23</citedby><cites>FETCH-LOGICAL-c466t-afb2a81187d1585f5db0185d76dc0b074cb027f2dfd5c354a1036f5b0c8f24c23</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,3356,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=16697860$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/15824148$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>PERRIGOUE, Jacqueline G</creatorcontrib><creatorcontrib>DEN BOON, Johan A</creatorcontrib><creatorcontrib>FRIEDL, Andreas</creatorcontrib><creatorcontrib>NEWTON, Michael A</creatorcontrib><creatorcontrib>AHLQUIST, Paul</creatorcontrib><creatorcontrib>SUGDEN, Bill</creatorcontrib><title>Lack of Association between EBV and Breast Carcinoma</title><title>Cancer epidemiology, biomarkers & prevention</title><addtitle>Cancer Epidemiol Biomarkers Prev</addtitle><description>Multiple conflicting findings have been presented which indicate that EBV may be found in anywhere from 0% to 51% of breast
carcinomas. When EBV has been found causally associated with other human cancers, its DNA and one or more of its viral products
have been detected in most tumor cells of a given biopsy. To test whether EBV has such an association with breast cancer,
we measured the number of viral DNA molecules per cell in matched normal and tumor biopsies from 45 patients using real-time
quantitative PCR. In no case could EBV DNA consistently be detected, with either of two different probes, at levels above
0.1 molecules per cell in two sections of the tumor samples. These levels of detection match those detected in EBV-negative
cell lines and therefore likely represent noise in the assays. Equally importantly, the distribution of these low signals
was the same between tumors and their matched normal controls. We conclude that EBV does not contribute to the development
of breast cancers as it does to epithelial cancers such as nasopharyngeal and gastric carcinomas or to Burkitt's and Hodgkin's
lymphomas.</description><subject>Actins - genetics</subject><subject>Adult</subject><subject>Aged</subject><subject>Aged, 80 and over</subject><subject>Biological and medical sciences</subject><subject>breast cancer</subject><subject>Breast Neoplasms - classification</subject><subject>Breast Neoplasms - pathology</subject><subject>Breast Neoplasms - virology</subject><subject>Case-Control Studies</subject><subject>DNA, Viral - isolation & purification</subject><subject>EBV</subject><subject>etiology</subject><subject>Female</subject><subject>Gynecology. Andrology. Obstetrics</subject><subject>Herpesvirus 4, Human - isolation & purification</subject><subject>Humans</subject><subject>In Situ Hybridization - methods</subject><subject>Mammary gland diseases</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>real-time PCR</subject><subject>Reverse Transcriptase Polymerase Chain Reaction</subject><subject>Tumors</subject><issn>1055-9965</issn><issn>1538-7755</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2005</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqF0D1PwzAQgGELgfgo_ARQFmBKOSc-2xnbqnxIlWAAVstxbBpok2Knqvj3OGpRRyZ7eO5Oegm5pDCkFOUdBcS0KDgOpy9PKbAUBM8PyCnFXKZCIB7G_585IWchfAKAKBCPyUlckDHK5ClhM22-ktYloxBaU-uubpuktN3G2iaZjt8T3VTJ2FsdumSivambdqnPyZHTi2Avdu-AvN1PXyeP6ez54WkymqWGcd6l2pWZlpRKUcWD6LAqgUqsBK8MlCCYKSETLqtchSZHpink3GEJRrqMmSwfkJvt3pVvv9c2dGpZB2MXC93Ydh0UFyKTNPsfUpEzikUPcQuNb0Pw1qmVr5fa_ygKqu-q-maqb6ZiVwVM9V3j3NXuwLpc2mo_tQsZwfUO6GD0wnndmDrsHeeFkByiu926ef0x39TeKhOl9d4GG_POFWWKKQlF_gv81IxG</recordid><startdate>20050401</startdate><enddate>20050401</enddate><creator>PERRIGOUE, Jacqueline G</creator><creator>DEN BOON, Johan A</creator><creator>FRIEDL, Andreas</creator><creator>NEWTON, Michael A</creator><creator>AHLQUIST, Paul</creator><creator>SUGDEN, Bill</creator><general>American Association for Cancer Research</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>20050401</creationdate><title>Lack of Association between EBV and Breast Carcinoma</title><author>PERRIGOUE, Jacqueline G ; DEN BOON, Johan A ; FRIEDL, Andreas ; NEWTON, Michael A ; AHLQUIST, Paul ; SUGDEN, Bill</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c466t-afb2a81187d1585f5db0185d76dc0b074cb027f2dfd5c354a1036f5b0c8f24c23</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2005</creationdate><topic>Actins - genetics</topic><topic>Adult</topic><topic>Aged</topic><topic>Aged, 80 and over</topic><topic>Biological and medical sciences</topic><topic>breast cancer</topic><topic>Breast Neoplasms - classification</topic><topic>Breast Neoplasms - pathology</topic><topic>Breast Neoplasms - virology</topic><topic>Case-Control Studies</topic><topic>DNA, Viral - isolation & purification</topic><topic>EBV</topic><topic>etiology</topic><topic>Female</topic><topic>Gynecology. Andrology. Obstetrics</topic><topic>Herpesvirus 4, Human - isolation & purification</topic><topic>Humans</topic><topic>In Situ Hybridization - methods</topic><topic>Mammary gland diseases</topic><topic>Medical sciences</topic><topic>Middle Aged</topic><topic>real-time PCR</topic><topic>Reverse Transcriptase Polymerase Chain Reaction</topic><topic>Tumors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>PERRIGOUE, Jacqueline G</creatorcontrib><creatorcontrib>DEN BOON, Johan A</creatorcontrib><creatorcontrib>FRIEDL, Andreas</creatorcontrib><creatorcontrib>NEWTON, Michael A</creatorcontrib><creatorcontrib>AHLQUIST, Paul</creatorcontrib><creatorcontrib>SUGDEN, Bill</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>Cancer epidemiology, biomarkers & prevention</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>PERRIGOUE, Jacqueline G</au><au>DEN BOON, Johan A</au><au>FRIEDL, Andreas</au><au>NEWTON, Michael A</au><au>AHLQUIST, Paul</au><au>SUGDEN, Bill</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Lack of Association between EBV and Breast Carcinoma</atitle><jtitle>Cancer epidemiology, biomarkers & prevention</jtitle><addtitle>Cancer Epidemiol Biomarkers Prev</addtitle><date>2005-04-01</date><risdate>2005</risdate><volume>14</volume><issue>4</issue><spage>809</spage><epage>814</epage><pages>809-814</pages><issn>1055-9965</issn><eissn>1538-7755</eissn><abstract>Multiple conflicting findings have been presented which indicate that EBV may be found in anywhere from 0% to 51% of breast
carcinomas. When EBV has been found causally associated with other human cancers, its DNA and one or more of its viral products
have been detected in most tumor cells of a given biopsy. To test whether EBV has such an association with breast cancer,
we measured the number of viral DNA molecules per cell in matched normal and tumor biopsies from 45 patients using real-time
quantitative PCR. In no case could EBV DNA consistently be detected, with either of two different probes, at levels above
0.1 molecules per cell in two sections of the tumor samples. These levels of detection match those detected in EBV-negative
cell lines and therefore likely represent noise in the assays. Equally importantly, the distribution of these low signals
was the same between tumors and their matched normal controls. We conclude that EBV does not contribute to the development
of breast cancers as it does to epithelial cancers such as nasopharyngeal and gastric carcinomas or to Burkitt's and Hodgkin's
lymphomas.</abstract><cop>Philadelphia, PA</cop><pub>American Association for Cancer Research</pub><pmid>15824148</pmid><doi>10.1158/1055-9965.EPI-04-0763</doi><tpages>6</tpages></addata></record> |
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source | MEDLINE; American Association for Cancer Research; EZB-FREE-00999 freely available EZB journals |
subjects | Actins - genetics Adult Aged Aged, 80 and over Biological and medical sciences breast cancer Breast Neoplasms - classification Breast Neoplasms - pathology Breast Neoplasms - virology Case-Control Studies DNA, Viral - isolation & purification EBV etiology Female Gynecology. Andrology. Obstetrics Herpesvirus 4, Human - isolation & purification Humans In Situ Hybridization - methods Mammary gland diseases Medical sciences Middle Aged real-time PCR Reverse Transcriptase Polymerase Chain Reaction Tumors |
title | Lack of Association between EBV and Breast Carcinoma |
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