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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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Autores principales: Fabris, Victoria, Abascal, María F, Giulianelli, Sebastián, May, María, Sequeira, Gonzalo R, Jacobsen, Britta, Lombès, Marc, Han, Julie, Tran, Luan, Molinolo, Alfredo, Lanari, Claudia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2017
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Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5653926/
https://www.ncbi.nlm.nih.gov/pubmed/29085663
http://dx.doi.org/10.1002/cjp2.83
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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_facet 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 Fabris, Victoria
collection PubMed
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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spelling pubmed-56539262017-10-30 Isoform specificity of progesterone receptor antibodies Fabris, Victoria Abascal, María F Giulianelli, Sebastián May, María Sequeira, Gonzalo R Jacobsen, Britta Lombès, Marc Han, Julie Tran, Luan Molinolo, Alfredo Lanari, Claudia J Pathol Clin Res Brief Definitive Report 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. John Wiley and Sons Inc. 2017-10-10 /pmc/articles/PMC5653926/ /pubmed/29085663 http://dx.doi.org/10.1002/cjp2.83 Text en © 2017 The Authors The Journal of Pathology: Clinical Research published by The Pathological Society of Great Britain and Ireland and John Wiley & Sons Ltd This is an open access article under the terms of the Creative Commons Attribution‐NonCommercial (http://creativecommons.org/licenses/by-nc/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.
spellingShingle Brief Definitive Report
Fabris, Victoria
Abascal, María F
Giulianelli, Sebastián
May, María
Sequeira, Gonzalo R
Jacobsen, Britta
Lombès, Marc
Han, Julie
Tran, Luan
Molinolo, Alfredo
Lanari, Claudia
Isoform specificity of progesterone receptor antibodies
title Isoform specificity of progesterone receptor antibodies
title_full Isoform specificity of progesterone receptor antibodies
title_fullStr Isoform specificity of progesterone receptor antibodies
title_full_unstemmed Isoform specificity of progesterone receptor antibodies
title_short Isoform specificity of progesterone receptor antibodies
title_sort isoform specificity of progesterone receptor antibodies
topic Brief Definitive Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5653926/
https://www.ncbi.nlm.nih.gov/pubmed/29085663
http://dx.doi.org/10.1002/cjp2.83
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