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
Hauptverfasser: Byrne, David J, Deb, Siddhartha, Takano, Elena A, Fox, Stephen B
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container_title Histopathology
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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
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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 &amp; Sons Ltd</rights><rights>2017 John Wiley &amp; Sons Ltd.</rights><rights>Copyright © 2017 John Wiley &amp; 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 ; 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source MEDLINE; Wiley Online Library Journals Frontfile Complete
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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