HER‐2 and cancer antigen 125 evaluation in ovarian borderline tumors by immunohistochemistry and fluorescence in situ hybridization

. The study determined the expression of cancer antigen (CA) 125 and HER‐2 in 45 borderline ovarian tumors (BOTs) and investigated the correlation of these biologic markers with histologic type, clinical stage, and outcome. The level of CA 125 protein was assessed using DAKO's M‐11 clone antibo...

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Veröffentlicht in:International journal of gynecological cancer 2004-11, Vol.14 (6), p.1078-1085
Hauptverfasser: Heinrich, J. K. R., Böttcher‐Luiz, F., Andrade, L. L. A., Davidson, S., Bonds, L., Stephens, J., Varella‐Garcia, M.
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container_end_page 1085
container_issue 6
container_start_page 1078
container_title International journal of gynecological cancer
container_volume 14
creator Heinrich, J. K. R.
Böttcher‐Luiz, F.
Andrade, L. L. A.
Davidson, S.
Bonds, L.
Stephens, J.
Varella‐Garcia, M.
description . The study determined the expression of cancer antigen (CA) 125 and HER‐2 in 45 borderline ovarian tumors (BOTs) and investigated the correlation of these biologic markers with histologic type, clinical stage, and outcome. The level of CA 125 protein was assessed using DAKO's M‐11 clone antibody in immunohistochemistry (IHC) assays (Carpinteria, CA). The HER‐2 protein expression was assessed in IHC assays using the HercepTest (DAKO), and the HER‐2 gene copy number per cell was investigated through fluorescence in situ hybridization (FISH) assays using VYSIS' PathVysion DNA Probe (Downers Grove, IL). Expression of the CA 125 protein was detected in 49% of the samples (22 out of 45 tumors) and significantly associated with the serous histologic type. However, CA 125 expression did not associate with clinical stage or outcome. Protein overexpression or gene amplification of HER‐2 was not found. However, abnormal FISH results were detected in 16% (seven out of 45 patients) of specimens comprising extranumerary copies of HER‐2 and/or chromosome 17 per cell. Abnormal FISH results were found to be independent of CA 125 expression and histologic type whereas they positively associate with advanced clinical stage. Our data show that HER‐2 is not altered in BOTs, and the presence of aneusomy for chromosome 17 and HER‐2 may predict tumor progression.
doi_str_mv 10.1111/j.1048-891X.2004.14605.x
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K. R. ; Böttcher‐Luiz, F. ; Andrade, L. L. A. ; Davidson, S. ; Bonds, L. ; Stephens, J. ; Varella‐Garcia, M.</creator><creatorcontrib>Heinrich, J. K. R. ; Böttcher‐Luiz, F. ; Andrade, L. L. A. ; Davidson, S. ; Bonds, L. ; Stephens, J. ; Varella‐Garcia, M.</creatorcontrib><description>. The study determined the expression of cancer antigen (CA) 125 and HER‐2 in 45 borderline ovarian tumors (BOTs) and investigated the correlation of these biologic markers with histologic type, clinical stage, and outcome. The level of CA 125 protein was assessed using DAKO's M‐11 clone antibody in immunohistochemistry (IHC) assays (Carpinteria, CA). The HER‐2 protein expression was assessed in IHC assays using the HercepTest (DAKO), and the HER‐2 gene copy number per cell was investigated through fluorescence in situ hybridization (FISH) assays using VYSIS' PathVysion DNA Probe (Downers Grove, IL). Expression of the CA 125 protein was detected in 49% of the samples (22 out of 45 tumors) and significantly associated with the serous histologic type. However, CA 125 expression did not associate with clinical stage or outcome. Protein overexpression or gene amplification of HER‐2 was not found. However, abnormal FISH results were detected in 16% (seven out of 45 patients) of specimens comprising extranumerary copies of HER‐2 and/or chromosome 17 per cell. Abnormal FISH results were found to be independent of CA 125 expression and histologic type whereas they positively associate with advanced clinical stage. Our data show that HER‐2 is not altered in BOTs, and the presence of aneusomy for chromosome 17 and HER‐2 may predict tumor progression.</description><identifier>ISSN: 1048-891X</identifier><identifier>EISSN: 1525-1438</identifier><identifier>DOI: 10.1111/j.1048-891X.2004.14605.x</identifier><identifier>PMID: 15571613</identifier><language>eng</language><publisher>Oxford, UK; Malden, USA: Blackwell Science Inc</publisher><subject>Adenocarcinoma, Mucinous - metabolism ; Biomarkers, Tumor - metabolism ; borderline ovarian tumors ; CA 125 ; CA-125 Antigen - metabolism ; Case-Control Studies ; Cystadenocarcinoma, Serous - metabolism ; Disease Progression ; Female ; FISH ; Gene Expression Regulation, Neoplastic ; HER‐2 ; Humans ; IHC ; Immunohistochemistry ; In Situ Hybridization, Fluorescence ; Ovarian Neoplasms - metabolism ; Paraffin Embedding ; Predictive Value of Tests ; Receptor, ErbB-2 - metabolism ; Retrospective Studies</subject><ispartof>International journal of gynecological cancer, 2004-11, Vol.14 (6), p.1078-1085</ispartof><rights>Copyright © 2004 Blackwell Publishing Ltd.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4134-db2b92c438b85f72ff5a5cc013982d8b599dabfac3c65f1b59717824d968fa9e3</citedby><cites>FETCH-LOGICAL-c4134-db2b92c438b85f72ff5a5cc013982d8b599dabfac3c65f1b59717824d968fa9e3</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.1048-891X.2004.14605.x$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2Fj.1048-891X.2004.14605.x$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,780,784,1416,27922,27923,45572,45573</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/15571613$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Heinrich, J. K. R.</creatorcontrib><creatorcontrib>Böttcher‐Luiz, F.</creatorcontrib><creatorcontrib>Andrade, L. L. A.</creatorcontrib><creatorcontrib>Davidson, S.</creatorcontrib><creatorcontrib>Bonds, L.</creatorcontrib><creatorcontrib>Stephens, J.</creatorcontrib><creatorcontrib>Varella‐Garcia, M.</creatorcontrib><title>HER‐2 and cancer antigen 125 evaluation in ovarian borderline tumors by immunohistochemistry and fluorescence in situ hybridization</title><title>International journal of gynecological cancer</title><addtitle>Int J Gynecol Cancer</addtitle><description>. The study determined the expression of cancer antigen (CA) 125 and HER‐2 in 45 borderline ovarian tumors (BOTs) and investigated the correlation of these biologic markers with histologic type, clinical stage, and outcome. The level of CA 125 protein was assessed using DAKO's M‐11 clone antibody in immunohistochemistry (IHC) assays (Carpinteria, CA). The HER‐2 protein expression was assessed in IHC assays using the HercepTest (DAKO), and the HER‐2 gene copy number per cell was investigated through fluorescence in situ hybridization (FISH) assays using VYSIS' PathVysion DNA Probe (Downers Grove, IL). Expression of the CA 125 protein was detected in 49% of the samples (22 out of 45 tumors) and significantly associated with the serous histologic type. However, CA 125 expression did not associate with clinical stage or outcome. Protein overexpression or gene amplification of HER‐2 was not found. However, abnormal FISH results were detected in 16% (seven out of 45 patients) of specimens comprising extranumerary copies of HER‐2 and/or chromosome 17 per cell. Abnormal FISH results were found to be independent of CA 125 expression and histologic type whereas they positively associate with advanced clinical stage. Our data show that HER‐2 is not altered in BOTs, and the presence of aneusomy for chromosome 17 and HER‐2 may predict tumor progression.</description><subject>Adenocarcinoma, Mucinous - metabolism</subject><subject>Biomarkers, Tumor - metabolism</subject><subject>borderline ovarian tumors</subject><subject>CA 125</subject><subject>CA-125 Antigen - metabolism</subject><subject>Case-Control Studies</subject><subject>Cystadenocarcinoma, Serous - metabolism</subject><subject>Disease Progression</subject><subject>Female</subject><subject>FISH</subject><subject>Gene Expression Regulation, Neoplastic</subject><subject>HER‐2</subject><subject>Humans</subject><subject>IHC</subject><subject>Immunohistochemistry</subject><subject>In Situ Hybridization, Fluorescence</subject><subject>Ovarian Neoplasms - metabolism</subject><subject>Paraffin Embedding</subject><subject>Predictive Value of Tests</subject><subject>Receptor, ErbB-2 - metabolism</subject><subject>Retrospective Studies</subject><issn>1048-891X</issn><issn>1525-1438</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2004</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNUU1v1TAQjBCIlsJfQD5xy6vXsRPngoSqfqFKSAgkbpbjbIgfTlzspG04cemd38gvwXnvIa74srvWzHg9k2UE6AbSOd1ugHKZyxq-bBilfAO8pGLz8CQ7BsFEDryQT1P_F3SUvYhxSymtGa2fZ0cgRAUlFMfZ49X5x98_fzGix5YYPRoMqZ3sVxwJMEHwTrtZT9aPxI7E3-lg9UgaH1oMzo5IpnnwIZJmIXYY5tH3Nk7e9DikGpadbOdmHzAaTOqrSrTTTPqlCba1P3baL7NnnXYRXx3qSfb54vzT2VV-8-Hy-uzdTW44FDxvG9bUzKTPNVJ0Fes6oYUxFIpaslY2oq5b3XTaFKYUHaS5gkoy3tal7HSNxUn2Zq97G_z3GeOk0poGndMj-jmqsgIOXMgElHugCT7GgJ26DXbQYVFA1RqB2qrVXbW6q9YI1C4C9ZCorw9vzM2A7T_iwfME4HvAvXcThvjNzfcYVI_aTb2ia0qiqvJVFCBN-XrFE-3tgWYdLv-9j7p-f7lriz_16KjX</recordid><startdate>200411</startdate><enddate>200411</enddate><creator>Heinrich, J. K. R.</creator><creator>Böttcher‐Luiz, F.</creator><creator>Andrade, L. L. A.</creator><creator>Davidson, S.</creator><creator>Bonds, L.</creator><creator>Stephens, J.</creator><creator>Varella‐Garcia, M.</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>7X8</scope></search><sort><creationdate>200411</creationdate><title>HER‐2 and cancer antigen 125 evaluation in ovarian borderline tumors by immunohistochemistry and fluorescence in situ hybridization</title><author>Heinrich, J. K. R. ; Böttcher‐Luiz, F. ; Andrade, L. L. A. ; Davidson, S. ; Bonds, L. ; Stephens, J. ; Varella‐Garcia, M.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4134-db2b92c438b85f72ff5a5cc013982d8b599dabfac3c65f1b59717824d968fa9e3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2004</creationdate><topic>Adenocarcinoma, Mucinous - metabolism</topic><topic>Biomarkers, Tumor - metabolism</topic><topic>borderline ovarian tumors</topic><topic>CA 125</topic><topic>CA-125 Antigen - metabolism</topic><topic>Case-Control Studies</topic><topic>Cystadenocarcinoma, Serous - metabolism</topic><topic>Disease Progression</topic><topic>Female</topic><topic>FISH</topic><topic>Gene Expression Regulation, Neoplastic</topic><topic>HER‐2</topic><topic>Humans</topic><topic>IHC</topic><topic>Immunohistochemistry</topic><topic>In Situ Hybridization, Fluorescence</topic><topic>Ovarian Neoplasms - metabolism</topic><topic>Paraffin Embedding</topic><topic>Predictive Value of Tests</topic><topic>Receptor, ErbB-2 - metabolism</topic><topic>Retrospective Studies</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Heinrich, J. K. R.</creatorcontrib><creatorcontrib>Böttcher‐Luiz, F.</creatorcontrib><creatorcontrib>Andrade, L. L. A.</creatorcontrib><creatorcontrib>Davidson, S.</creatorcontrib><creatorcontrib>Bonds, L.</creatorcontrib><creatorcontrib>Stephens, J.</creatorcontrib><creatorcontrib>Varella‐Garcia, M.</creatorcontrib><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>International journal of gynecological cancer</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Heinrich, J. K. R.</au><au>Böttcher‐Luiz, F.</au><au>Andrade, L. L. A.</au><au>Davidson, S.</au><au>Bonds, L.</au><au>Stephens, J.</au><au>Varella‐Garcia, M.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>HER‐2 and cancer antigen 125 evaluation in ovarian borderline tumors by immunohistochemistry and fluorescence in situ hybridization</atitle><jtitle>International journal of gynecological cancer</jtitle><addtitle>Int J Gynecol Cancer</addtitle><date>2004-11</date><risdate>2004</risdate><volume>14</volume><issue>6</issue><spage>1078</spage><epage>1085</epage><pages>1078-1085</pages><issn>1048-891X</issn><eissn>1525-1438</eissn><abstract>. The study determined the expression of cancer antigen (CA) 125 and HER‐2 in 45 borderline ovarian tumors (BOTs) and investigated the correlation of these biologic markers with histologic type, clinical stage, and outcome. The level of CA 125 protein was assessed using DAKO's M‐11 clone antibody in immunohistochemistry (IHC) assays (Carpinteria, CA). The HER‐2 protein expression was assessed in IHC assays using the HercepTest (DAKO), and the HER‐2 gene copy number per cell was investigated through fluorescence in situ hybridization (FISH) assays using VYSIS' PathVysion DNA Probe (Downers Grove, IL). Expression of the CA 125 protein was detected in 49% of the samples (22 out of 45 tumors) and significantly associated with the serous histologic type. However, CA 125 expression did not associate with clinical stage or outcome. Protein overexpression or gene amplification of HER‐2 was not found. However, abnormal FISH results were detected in 16% (seven out of 45 patients) of specimens comprising extranumerary copies of HER‐2 and/or chromosome 17 per cell. Abnormal FISH results were found to be independent of CA 125 expression and histologic type whereas they positively associate with advanced clinical stage. Our data show that HER‐2 is not altered in BOTs, and the presence of aneusomy for chromosome 17 and HER‐2 may predict tumor progression.</abstract><cop>Oxford, UK; Malden, USA</cop><pub>Blackwell Science Inc</pub><pmid>15571613</pmid><doi>10.1111/j.1048-891X.2004.14605.x</doi><tpages>8</tpages></addata></record>
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subjects Adenocarcinoma, Mucinous - metabolism
Biomarkers, Tumor - metabolism
borderline ovarian tumors
CA 125
CA-125 Antigen - metabolism
Case-Control Studies
Cystadenocarcinoma, Serous - metabolism
Disease Progression
Female
FISH
Gene Expression Regulation, Neoplastic
HER‐2
Humans
IHC
Immunohistochemistry
In Situ Hybridization, Fluorescence
Ovarian Neoplasms - metabolism
Paraffin Embedding
Predictive Value of Tests
Receptor, ErbB-2 - metabolism
Retrospective Studies
title HER‐2 and cancer antigen 125 evaluation in ovarian borderline tumors by immunohistochemistry and fluorescence in situ hybridization
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