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...
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Veröffentlicht in: | The journal of pathology. Clinical research 2017-10, Vol.3 (4), p.227-233 |
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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. |
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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 & 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 & 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 & 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 & 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 & Medical Complete (Alumni)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health & 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 & 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> |
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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 |
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