GATA3 expression in triple‐negative breast cancers
Aims GATA‐binding protein 3 (GATA3) is a well‐studied transcription factor found to be essential in the development of luminal breast epithelium and has been identified in a variety of tumour types, including breast and urothelial carcinomas, making it a useful immunohistochemistry marker in the dia...
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Veröffentlicht in: | Histopathology 2017-07, Vol.71 (1), p.63-71 |
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creator | Byrne, David J Deb, Siddhartha Takano, Elena A Fox, Stephen B |
description | Aims
GATA‐binding protein 3 (GATA3) is a well‐studied transcription factor found to be essential in the development of luminal breast epithelium and has been identified in a variety of tumour types, including breast and urothelial carcinomas, making it a useful immunohistochemistry marker in the diagnosis of both primary and metastatic disease.
Methods and results
We investigated GATA3 protein expression in a 106 primary triple‐negative breast carcinomas (100 basal‐like, six non‐basal‐like) using Cell Marque mouse monoclonal anti‐GATA3 (L50‐823). Reverse transcription–quantitative polymerase chain reaction (RT–qPCR) was used to quantify mRNA expression in 22 triple‐negative breast cancers (TNBCs) (20 primary and two cell lines), four luminal (three primary and one cell line) and five human epidermal growth factor receptor 2 (HER2) (four primary and one cell line) amplified tumours. In 98 TNBCs where IHC was assessable, 47 (48%) had a 1+ or greater staining with 20 (21%) having high GATA3 expression when using a weighted scoring.
Conclusion
Our study has demonstrated that GATA3 expression is common in primary triple‐negative breast carcinomas. It also suggests that although GATA3 is an oestrogen receptor (ER) regulated gene, it still proves useful in differentiating between primary and metastatic tumours in patients with a history of breast cancer regardless of its molecular subtype. |
doi_str_mv | 10.1111/his.13187 |
format | Article |
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GATA‐binding protein 3 (GATA3) is a well‐studied transcription factor found to be essential in the development of luminal breast epithelium and has been identified in a variety of tumour types, including breast and urothelial carcinomas, making it a useful immunohistochemistry marker in the diagnosis of both primary and metastatic disease.
Methods and results
We investigated GATA3 protein expression in a 106 primary triple‐negative breast carcinomas (100 basal‐like, six non‐basal‐like) using Cell Marque mouse monoclonal anti‐GATA3 (L50‐823). Reverse transcription–quantitative polymerase chain reaction (RT–qPCR) was used to quantify mRNA expression in 22 triple‐negative breast cancers (TNBCs) (20 primary and two cell lines), four luminal (three primary and one cell line) and five human epidermal growth factor receptor 2 (HER2) (four primary and one cell line) amplified tumours. In 98 TNBCs where IHC was assessable, 47 (48%) had a 1+ or greater staining with 20 (21%) having high GATA3 expression when using a weighted scoring.
Conclusion
Our study has demonstrated that GATA3 expression is common in primary triple‐negative breast carcinomas. It also suggests that although GATA3 is an oestrogen receptor (ER) regulated gene, it still proves useful in differentiating between primary and metastatic tumours in patients with a history of breast cancer regardless of its molecular subtype.</description><identifier>ISSN: 0309-0167</identifier><identifier>EISSN: 1365-2559</identifier><identifier>DOI: 10.1111/his.13187</identifier><identifier>PMID: 28211079</identifier><language>eng</language><publisher>England: Wiley Subscription Services, Inc</publisher><subject>Adult ; Aged ; Biomarkers, Tumor - analysis ; Breast cancer ; Breast carcinoma ; Epidermal growth factor ; Epithelium ; ErbB-2 protein ; Female ; GATA-3 protein ; GATA-binding protein ; GATA3 ; GATA3 Transcription Factor - analysis ; GATA3 Transcription Factor - biosynthesis ; Gene expression ; Humans ; Immunohistochemistry ; Metastases ; Metastasis ; Middle Aged ; Polymerase chain reaction ; Reverse transcription ; Rodents ; Staining ; TNBC ; Triple Negative Breast Neoplasms - metabolism ; Tumors ; Urothelial carcinoma</subject><ispartof>Histopathology, 2017-07, Vol.71 (1), p.63-71</ispartof><rights>2017 John Wiley & Sons Ltd</rights><rights>2017 John Wiley & Sons Ltd.</rights><rights>Copyright © 2017 John Wiley & Sons Ltd</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3887-3e089bc929498e962dff01cfa0bf4b830e8463de46e6f0b95fad60a6c6c2f87f3</citedby><cites>FETCH-LOGICAL-c3887-3e089bc929498e962dff01cfa0bf4b830e8463de46e6f0b95fad60a6c6c2f87f3</cites><orcidid>0000-0002-9258-3252</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1111%2Fhis.13187$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2Fhis.13187$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,776,780,1411,27901,27902,45550,45551</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/28211079$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Byrne, David J</creatorcontrib><creatorcontrib>Deb, Siddhartha</creatorcontrib><creatorcontrib>Takano, Elena A</creatorcontrib><creatorcontrib>Fox, Stephen B</creatorcontrib><title>GATA3 expression in triple‐negative breast cancers</title><title>Histopathology</title><addtitle>Histopathology</addtitle><description>Aims
GATA‐binding protein 3 (GATA3) is a well‐studied transcription factor found to be essential in the development of luminal breast epithelium and has been identified in a variety of tumour types, including breast and urothelial carcinomas, making it a useful immunohistochemistry marker in the diagnosis of both primary and metastatic disease.
Methods and results
We investigated GATA3 protein expression in a 106 primary triple‐negative breast carcinomas (100 basal‐like, six non‐basal‐like) using Cell Marque mouse monoclonal anti‐GATA3 (L50‐823). Reverse transcription–quantitative polymerase chain reaction (RT–qPCR) was used to quantify mRNA expression in 22 triple‐negative breast cancers (TNBCs) (20 primary and two cell lines), four luminal (three primary and one cell line) and five human epidermal growth factor receptor 2 (HER2) (four primary and one cell line) amplified tumours. In 98 TNBCs where IHC was assessable, 47 (48%) had a 1+ or greater staining with 20 (21%) having high GATA3 expression when using a weighted scoring.
Conclusion
Our study has demonstrated that GATA3 expression is common in primary triple‐negative breast carcinomas. It also suggests that although GATA3 is an oestrogen receptor (ER) regulated gene, it still proves useful in differentiating between primary and metastatic tumours in patients with a history of breast cancer regardless of its molecular subtype.</description><subject>Adult</subject><subject>Aged</subject><subject>Biomarkers, Tumor - analysis</subject><subject>Breast cancer</subject><subject>Breast carcinoma</subject><subject>Epidermal growth factor</subject><subject>Epithelium</subject><subject>ErbB-2 protein</subject><subject>Female</subject><subject>GATA-3 protein</subject><subject>GATA-binding protein</subject><subject>GATA3</subject><subject>GATA3 Transcription Factor - analysis</subject><subject>GATA3 Transcription Factor - biosynthesis</subject><subject>Gene expression</subject><subject>Humans</subject><subject>Immunohistochemistry</subject><subject>Metastases</subject><subject>Metastasis</subject><subject>Middle Aged</subject><subject>Polymerase chain reaction</subject><subject>Reverse transcription</subject><subject>Rodents</subject><subject>Staining</subject><subject>TNBC</subject><subject>Triple Negative Breast Neoplasms - metabolism</subject><subject>Tumors</subject><subject>Urothelial carcinoma</subject><issn>0309-0167</issn><issn>1365-2559</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp10L1OwzAUhmELgWgpDNwAisQCQ4p_EsceqwraSpUYKLPlOMeQKk2CnQDduASukSshkMKAhBcvj14dfQidEjwm3bt6zP2YMCKSPTQkjMchjWO5j4aYYRliwpMBOvJ-jTFJGKWHaEAFJQQncoii2WQ1YQG81g68z6syyMugcXldwMfbewkPusmfIUgdaN8ERpcGnD9GB1YXHk52_wjd31yvpvNweTtbTCfL0DAhkpABFjI1kspICpCcZtZiYqzGqY1SwTCIiLMMIg7c4lTGVmcca264oVYklo3QRd-tXfXUgm_UJvcGikKXULVeEcGl5ILGuKPnf-i6al3ZXaeIxAllcSSjTl32yrjKewdW1S7faLdVBKuvKVU3pfqesrNnu2KbbiD7lT_bdeCqBy95Adv_S2q-uOuTnx0GfJM</recordid><startdate>201707</startdate><enddate>201707</enddate><creator>Byrne, David J</creator><creator>Deb, Siddhartha</creator><creator>Takano, Elena A</creator><creator>Fox, Stephen B</creator><general>Wiley Subscription Services, Inc</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>7QP</scope><scope>7QR</scope><scope>7T5</scope><scope>7TK</scope><scope>7TM</scope><scope>8FD</scope><scope>FR3</scope><scope>H94</scope><scope>P64</scope><scope>RC3</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0002-9258-3252</orcidid></search><sort><creationdate>201707</creationdate><title>GATA3 expression in triple‐negative breast cancers</title><author>Byrne, David J ; Deb, Siddhartha ; Takano, Elena A ; Fox, Stephen B</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3887-3e089bc929498e962dff01cfa0bf4b830e8463de46e6f0b95fad60a6c6c2f87f3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>Adult</topic><topic>Aged</topic><topic>Biomarkers, Tumor - analysis</topic><topic>Breast cancer</topic><topic>Breast carcinoma</topic><topic>Epidermal growth factor</topic><topic>Epithelium</topic><topic>ErbB-2 protein</topic><topic>Female</topic><topic>GATA-3 protein</topic><topic>GATA-binding protein</topic><topic>GATA3</topic><topic>GATA3 Transcription Factor - analysis</topic><topic>GATA3 Transcription Factor - biosynthesis</topic><topic>Gene expression</topic><topic>Humans</topic><topic>Immunohistochemistry</topic><topic>Metastases</topic><topic>Metastasis</topic><topic>Middle Aged</topic><topic>Polymerase chain reaction</topic><topic>Reverse transcription</topic><topic>Rodents</topic><topic>Staining</topic><topic>TNBC</topic><topic>Triple Negative Breast Neoplasms - metabolism</topic><topic>Tumors</topic><topic>Urothelial carcinoma</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Byrne, David J</creatorcontrib><creatorcontrib>Deb, Siddhartha</creatorcontrib><creatorcontrib>Takano, Elena A</creatorcontrib><creatorcontrib>Fox, Stephen B</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Chemoreception Abstracts</collection><collection>Immunology Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>Nucleic Acids 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>Histopathology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Byrne, David J</au><au>Deb, Siddhartha</au><au>Takano, Elena A</au><au>Fox, Stephen B</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>GATA3 expression in triple‐negative breast cancers</atitle><jtitle>Histopathology</jtitle><addtitle>Histopathology</addtitle><date>2017-07</date><risdate>2017</risdate><volume>71</volume><issue>1</issue><spage>63</spage><epage>71</epage><pages>63-71</pages><issn>0309-0167</issn><eissn>1365-2559</eissn><abstract>Aims
GATA‐binding protein 3 (GATA3) is a well‐studied transcription factor found to be essential in the development of luminal breast epithelium and has been identified in a variety of tumour types, including breast and urothelial carcinomas, making it a useful immunohistochemistry marker in the diagnosis of both primary and metastatic disease.
Methods and results
We investigated GATA3 protein expression in a 106 primary triple‐negative breast carcinomas (100 basal‐like, six non‐basal‐like) using Cell Marque mouse monoclonal anti‐GATA3 (L50‐823). Reverse transcription–quantitative polymerase chain reaction (RT–qPCR) was used to quantify mRNA expression in 22 triple‐negative breast cancers (TNBCs) (20 primary and two cell lines), four luminal (three primary and one cell line) and five human epidermal growth factor receptor 2 (HER2) (four primary and one cell line) amplified tumours. In 98 TNBCs where IHC was assessable, 47 (48%) had a 1+ or greater staining with 20 (21%) having high GATA3 expression when using a weighted scoring.
Conclusion
Our study has demonstrated that GATA3 expression is common in primary triple‐negative breast carcinomas. It also suggests that although GATA3 is an oestrogen receptor (ER) regulated gene, it still proves useful in differentiating between primary and metastatic tumours in patients with a history of breast cancer regardless of its molecular subtype.</abstract><cop>England</cop><pub>Wiley Subscription Services, Inc</pub><pmid>28211079</pmid><doi>10.1111/his.13187</doi><tpages>9</tpages><orcidid>https://orcid.org/0000-0002-9258-3252</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Adult Aged Biomarkers, Tumor - analysis Breast cancer Breast carcinoma Epidermal growth factor Epithelium ErbB-2 protein Female GATA-3 protein GATA-binding protein GATA3 GATA3 Transcription Factor - analysis GATA3 Transcription Factor - biosynthesis Gene expression Humans Immunohistochemistry Metastases Metastasis Middle Aged Polymerase chain reaction Reverse transcription Rodents Staining TNBC Triple Negative Breast Neoplasms - metabolism Tumors Urothelial carcinoma |
title | GATA3 expression in triple‐negative breast cancers |
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