Isoform specificity of progesterone receptor antibodies

Progesterone receptors (PR) are prognostic and predictive biomarkers in hormone‐dependent cancers. Two main PR isoforms have been described, PRB and PRA, that differ only in that PRB has 164 extra N‐terminal amino acids. It has been reported that several antibodies empirically exclusively recognize...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:The journal of pathology. Clinical research 2017-10, Vol.3 (4), p.227-233
Hauptverfasser: Fabris, Victoria, Abascal, María F, Giulianelli, Sebastián, May, María, Sequeira, Gonzalo R, Jacobsen, Britta, Lombès, Marc, Han, Julie, Tran, Luan, Molinolo, Alfredo, Lanari, Claudia
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 233
container_issue 4
container_start_page 227
container_title The journal of pathology. Clinical research
container_volume 3
creator Fabris, Victoria
Abascal, María F
Giulianelli, Sebastián
May, María
Sequeira, Gonzalo R
Jacobsen, Britta
Lombès, Marc
Han, Julie
Tran, Luan
Molinolo, Alfredo
Lanari, Claudia
description Progesterone receptors (PR) are prognostic and predictive biomarkers in hormone‐dependent cancers. Two main PR isoforms have been described, PRB and PRA, that differ only in that PRB has 164 extra N‐terminal amino acids. It has been reported that several antibodies empirically exclusively recognize PRA in formalin‐fixed paraffin‐embedded (FFPE) tissues. To confirm these findings, we used human breast cancer xenograft models, T47D‐YA and ‐YB cells expressing PRA or PRB, respectively, MDA‐MB‐231 cells modified to synthesize PRB, and MDA‐MB‐231/iPRAB cells which can bi‐inducibly express either PRA or PRB. Cells were injected into immunocompromised mice to generate tumours exclusively expressing PRA or PRB. PR isoform expression was verified using immunoblots. FFPE samples from the same tumours were studied by immunohistochemistry using H‐190, clone 636, clone 16, and Ab‐6 anti‐PR antibodies, the latter exclusively recognizing PRB. Except for Ab‐6, all antibodies displayed a similar staining pattern. Our results indicate that clones 16, 636, and the H‐190 antibody recognize both PR isoforms. They point to the need for more stringency in evaluating the true specificity of purported PRA‐specific antibodies as the PRA/PRB ratio may have prognostic and predictive value in breast cancer.
doi_str_mv 10.1002/cjp2.83
format Article
fullrecord <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_5653926</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2289933391</sourcerecordid><originalsourceid>FETCH-LOGICAL-c4613-a956814e003dba73cb24d5b1cbedfd646cfcf33eb4b4cf17120f504c21c556c53</originalsourceid><addsrcrecordid>eNp1kU1Lw0AQhhdRbKnFfyABDwrSut9JLoIUPyoFPeh5STazdUuSjbup0n9vSmupgqcZmIeHd2YQOiV4TDCm13rR0HHCDlCfYiFHXLDkcK_voWEIC4wxEQTHlB-jHk1xIqRkfRRPgzPOV1FoQFtjtW1XkTNR490cQgve1RB50NC0zkdZ3drcFRbCCToyWRlguK0D9HZ_9zp5HM2eH6aT29lIc0nYKEuFTAgHjFmRZzHTOeWFyInOoTCF5FIbbRiDnOdcGxITio3AXFOihZBasAG62XibZV5BoaFufVaqxtsq8yvlMqt-T2r7rubuUwkpWEplJ7jcCrz7WHYrqcoGDWWZ1eCWQZFUJIJJLkiHnv9BF27p6249RWmSpoyxdE1dbCjtXQgezC4MwWr9D7X-h0pYR57tZ99xP9fvgKsN8GVLWP3nUZOnF9rpvgHGb5QG</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2289933391</pqid></control><display><type>article</type><title>Isoform specificity of progesterone receptor antibodies</title><source>Wiley Online Library Open Access</source><source>DOAJ Directory of Open Access Journals</source><source>Wiley Online Library Journals Frontfile Complete</source><source>EZB-FREE-00999 freely available EZB journals</source><source>PubMed Central</source><creator>Fabris, Victoria ; Abascal, María F ; Giulianelli, Sebastián ; May, María ; Sequeira, Gonzalo R ; Jacobsen, Britta ; Lombès, Marc ; Han, Julie ; Tran, Luan ; Molinolo, Alfredo ; Lanari, Claudia</creator><creatorcontrib>Fabris, Victoria ; Abascal, María F ; Giulianelli, Sebastián ; May, María ; Sequeira, Gonzalo R ; Jacobsen, Britta ; Lombès, Marc ; Han, Julie ; Tran, Luan ; Molinolo, Alfredo ; Lanari, Claudia</creatorcontrib><description>Progesterone receptors (PR) are prognostic and predictive biomarkers in hormone‐dependent cancers. Two main PR isoforms have been described, PRB and PRA, that differ only in that PRB has 164 extra N‐terminal amino acids. It has been reported that several antibodies empirically exclusively recognize PRA in formalin‐fixed paraffin‐embedded (FFPE) tissues. To confirm these findings, we used human breast cancer xenograft models, T47D‐YA and ‐YB cells expressing PRA or PRB, respectively, MDA‐MB‐231 cells modified to synthesize PRB, and MDA‐MB‐231/iPRAB cells which can bi‐inducibly express either PRA or PRB. Cells were injected into immunocompromised mice to generate tumours exclusively expressing PRA or PRB. PR isoform expression was verified using immunoblots. FFPE samples from the same tumours were studied by immunohistochemistry using H‐190, clone 636, clone 16, and Ab‐6 anti‐PR antibodies, the latter exclusively recognizing PRB. Except for Ab‐6, all antibodies displayed a similar staining pattern. Our results indicate that clones 16, 636, and the H‐190 antibody recognize both PR isoforms. They point to the need for more stringency in evaluating the true specificity of purported PRA‐specific antibodies as the PRA/PRB ratio may have prognostic and predictive value in breast cancer.</description><identifier>ISSN: 2056-4538</identifier><identifier>EISSN: 2056-4538</identifier><identifier>DOI: 10.1002/cjp2.83</identifier><identifier>PMID: 29085663</identifier><language>eng</language><publisher>England: John Wiley &amp; Sons, Inc</publisher><subject>Antibodies ; Breast cancer ; breast cancer models ; Brief Definitive Report ; Cloning ; Immunoglobulins ; Immunohistochemistry ; Isoforms ; Laboratory animals ; Menopause ; Paraffin ; Progesterone ; progesterone receptor isoforms ; Progesterone receptors ; specific antibodies ; Studies ; Tumors ; Xenografts</subject><ispartof>The journal of pathology. Clinical research, 2017-10, Vol.3 (4), p.227-233</ispartof><rights>2017 The Authors The Journal of Pathology: Clinical Research published by The Pathological Society of Great Britain and Ireland and John Wiley &amp; Sons Ltd</rights><rights>2017. This work is published under http://creativecommons.org/licenses/by-nc/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4613-a956814e003dba73cb24d5b1cbedfd646cfcf33eb4b4cf17120f504c21c556c53</citedby><cites>FETCH-LOGICAL-c4613-a956814e003dba73cb24d5b1cbedfd646cfcf33eb4b4cf17120f504c21c556c53</cites><orcidid>0000-0003-0555-2309</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC5653926/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC5653926/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,860,881,1411,11541,27901,27902,45550,45551,46027,46451,53766,53768</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/29085663$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Fabris, Victoria</creatorcontrib><creatorcontrib>Abascal, María F</creatorcontrib><creatorcontrib>Giulianelli, Sebastián</creatorcontrib><creatorcontrib>May, María</creatorcontrib><creatorcontrib>Sequeira, Gonzalo R</creatorcontrib><creatorcontrib>Jacobsen, Britta</creatorcontrib><creatorcontrib>Lombès, Marc</creatorcontrib><creatorcontrib>Han, Julie</creatorcontrib><creatorcontrib>Tran, Luan</creatorcontrib><creatorcontrib>Molinolo, Alfredo</creatorcontrib><creatorcontrib>Lanari, Claudia</creatorcontrib><title>Isoform specificity of progesterone receptor antibodies</title><title>The journal of pathology. Clinical research</title><addtitle>J Pathol Clin Res</addtitle><description>Progesterone receptors (PR) are prognostic and predictive biomarkers in hormone‐dependent cancers. Two main PR isoforms have been described, PRB and PRA, that differ only in that PRB has 164 extra N‐terminal amino acids. It has been reported that several antibodies empirically exclusively recognize PRA in formalin‐fixed paraffin‐embedded (FFPE) tissues. To confirm these findings, we used human breast cancer xenograft models, T47D‐YA and ‐YB cells expressing PRA or PRB, respectively, MDA‐MB‐231 cells modified to synthesize PRB, and MDA‐MB‐231/iPRAB cells which can bi‐inducibly express either PRA or PRB. Cells were injected into immunocompromised mice to generate tumours exclusively expressing PRA or PRB. PR isoform expression was verified using immunoblots. FFPE samples from the same tumours were studied by immunohistochemistry using H‐190, clone 636, clone 16, and Ab‐6 anti‐PR antibodies, the latter exclusively recognizing PRB. Except for Ab‐6, all antibodies displayed a similar staining pattern. Our results indicate that clones 16, 636, and the H‐190 antibody recognize both PR isoforms. They point to the need for more stringency in evaluating the true specificity of purported PRA‐specific antibodies as the PRA/PRB ratio may have prognostic and predictive value in breast cancer.</description><subject>Antibodies</subject><subject>Breast cancer</subject><subject>breast cancer models</subject><subject>Brief Definitive Report</subject><subject>Cloning</subject><subject>Immunoglobulins</subject><subject>Immunohistochemistry</subject><subject>Isoforms</subject><subject>Laboratory animals</subject><subject>Menopause</subject><subject>Paraffin</subject><subject>Progesterone</subject><subject>progesterone receptor isoforms</subject><subject>Progesterone receptors</subject><subject>specific antibodies</subject><subject>Studies</subject><subject>Tumors</subject><subject>Xenografts</subject><issn>2056-4538</issn><issn>2056-4538</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><sourceid>24P</sourceid><sourceid>BENPR</sourceid><recordid>eNp1kU1Lw0AQhhdRbKnFfyABDwrSut9JLoIUPyoFPeh5STazdUuSjbup0n9vSmupgqcZmIeHd2YQOiV4TDCm13rR0HHCDlCfYiFHXLDkcK_voWEIC4wxEQTHlB-jHk1xIqRkfRRPgzPOV1FoQFtjtW1XkTNR490cQgve1RB50NC0zkdZ3drcFRbCCToyWRlguK0D9HZ_9zp5HM2eH6aT29lIc0nYKEuFTAgHjFmRZzHTOeWFyInOoTCF5FIbbRiDnOdcGxITio3AXFOihZBasAG62XibZV5BoaFufVaqxtsq8yvlMqt-T2r7rubuUwkpWEplJ7jcCrz7WHYrqcoGDWWZ1eCWQZFUJIJJLkiHnv9BF27p6249RWmSpoyxdE1dbCjtXQgezC4MwWr9D7X-h0pYR57tZ99xP9fvgKsN8GVLWP3nUZOnF9rpvgHGb5QG</recordid><startdate>201710</startdate><enddate>201710</enddate><creator>Fabris, Victoria</creator><creator>Abascal, María F</creator><creator>Giulianelli, Sebastián</creator><creator>May, María</creator><creator>Sequeira, Gonzalo R</creator><creator>Jacobsen, Britta</creator><creator>Lombès, Marc</creator><creator>Han, Julie</creator><creator>Tran, Luan</creator><creator>Molinolo, Alfredo</creator><creator>Lanari, Claudia</creator><general>John Wiley &amp; Sons, Inc</general><general>John Wiley and Sons Inc</general><scope>24P</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M7P</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0003-0555-2309</orcidid></search><sort><creationdate>201710</creationdate><title>Isoform specificity of progesterone receptor antibodies</title><author>Fabris, Victoria ; Abascal, María F ; Giulianelli, Sebastián ; May, María ; Sequeira, Gonzalo R ; Jacobsen, Britta ; Lombès, Marc ; Han, Julie ; Tran, Luan ; Molinolo, Alfredo ; Lanari, Claudia</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4613-a956814e003dba73cb24d5b1cbedfd646cfcf33eb4b4cf17120f504c21c556c53</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>Antibodies</topic><topic>Breast cancer</topic><topic>breast cancer models</topic><topic>Brief Definitive Report</topic><topic>Cloning</topic><topic>Immunoglobulins</topic><topic>Immunohistochemistry</topic><topic>Isoforms</topic><topic>Laboratory animals</topic><topic>Menopause</topic><topic>Paraffin</topic><topic>Progesterone</topic><topic>progesterone receptor isoforms</topic><topic>Progesterone receptors</topic><topic>specific antibodies</topic><topic>Studies</topic><topic>Tumors</topic><topic>Xenografts</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Fabris, Victoria</creatorcontrib><creatorcontrib>Abascal, María F</creatorcontrib><creatorcontrib>Giulianelli, Sebastián</creatorcontrib><creatorcontrib>May, María</creatorcontrib><creatorcontrib>Sequeira, Gonzalo R</creatorcontrib><creatorcontrib>Jacobsen, Britta</creatorcontrib><creatorcontrib>Lombès, Marc</creatorcontrib><creatorcontrib>Han, Julie</creatorcontrib><creatorcontrib>Tran, Luan</creatorcontrib><creatorcontrib>Molinolo, Alfredo</creatorcontrib><creatorcontrib>Lanari, Claudia</creatorcontrib><collection>Wiley Online Library Open Access</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Health &amp; Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health &amp; Medical Collection (Alumni Edition)</collection><collection>Biological Science Database</collection><collection>Publicly Available Content Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>The journal of pathology. Clinical research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Fabris, Victoria</au><au>Abascal, María F</au><au>Giulianelli, Sebastián</au><au>May, María</au><au>Sequeira, Gonzalo R</au><au>Jacobsen, Britta</au><au>Lombès, Marc</au><au>Han, Julie</au><au>Tran, Luan</au><au>Molinolo, Alfredo</au><au>Lanari, Claudia</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Isoform specificity of progesterone receptor antibodies</atitle><jtitle>The journal of pathology. Clinical research</jtitle><addtitle>J Pathol Clin Res</addtitle><date>2017-10</date><risdate>2017</risdate><volume>3</volume><issue>4</issue><spage>227</spage><epage>233</epage><pages>227-233</pages><issn>2056-4538</issn><eissn>2056-4538</eissn><abstract>Progesterone receptors (PR) are prognostic and predictive biomarkers in hormone‐dependent cancers. Two main PR isoforms have been described, PRB and PRA, that differ only in that PRB has 164 extra N‐terminal amino acids. It has been reported that several antibodies empirically exclusively recognize PRA in formalin‐fixed paraffin‐embedded (FFPE) tissues. To confirm these findings, we used human breast cancer xenograft models, T47D‐YA and ‐YB cells expressing PRA or PRB, respectively, MDA‐MB‐231 cells modified to synthesize PRB, and MDA‐MB‐231/iPRAB cells which can bi‐inducibly express either PRA or PRB. Cells were injected into immunocompromised mice to generate tumours exclusively expressing PRA or PRB. PR isoform expression was verified using immunoblots. FFPE samples from the same tumours were studied by immunohistochemistry using H‐190, clone 636, clone 16, and Ab‐6 anti‐PR antibodies, the latter exclusively recognizing PRB. Except for Ab‐6, all antibodies displayed a similar staining pattern. Our results indicate that clones 16, 636, and the H‐190 antibody recognize both PR isoforms. They point to the need for more stringency in evaluating the true specificity of purported PRA‐specific antibodies as the PRA/PRB ratio may have prognostic and predictive value in breast cancer.</abstract><cop>England</cop><pub>John Wiley &amp; Sons, Inc</pub><pmid>29085663</pmid><doi>10.1002/cjp2.83</doi><tpages>7</tpages><orcidid>https://orcid.org/0000-0003-0555-2309</orcidid><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 2056-4538
ispartof The journal of pathology. Clinical research, 2017-10, Vol.3 (4), p.227-233
issn 2056-4538
2056-4538
language eng
recordid cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_5653926
source Wiley Online Library Open Access; DOAJ Directory of Open Access Journals; Wiley Online Library Journals Frontfile Complete; EZB-FREE-00999 freely available EZB journals; PubMed Central
subjects Antibodies
Breast cancer
breast cancer models
Brief Definitive Report
Cloning
Immunoglobulins
Immunohistochemistry
Isoforms
Laboratory animals
Menopause
Paraffin
Progesterone
progesterone receptor isoforms
Progesterone receptors
specific antibodies
Studies
Tumors
Xenografts
title Isoform specificity of progesterone receptor antibodies
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-08T12%3A34%3A35IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_pubme&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Isoform%20specificity%20of%20progesterone%20receptor%20antibodies&rft.jtitle=The%20journal%20of%20pathology.%20Clinical%20research&rft.au=Fabris,%20Victoria&rft.date=2017-10&rft.volume=3&rft.issue=4&rft.spage=227&rft.epage=233&rft.pages=227-233&rft.issn=2056-4538&rft.eissn=2056-4538&rft_id=info:doi/10.1002/cjp2.83&rft_dat=%3Cproquest_pubme%3E2289933391%3C/proquest_pubme%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=2289933391&rft_id=info:pmid/29085663&rfr_iscdi=true