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Insufficient antibody validation challenges oestrogen receptor beta research
The discovery of oestrogen receptor β (ERβ/ESR2) was a landmark discovery. Its reported expression and homology with breast cancer pharmacological target ERα (ESR1) raised hopes for improved endocrine therapies. After 20 years of intense research, this has not materialized. We here perform a rigorou...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5501969/ https://www.ncbi.nlm.nih.gov/pubmed/28643774 http://dx.doi.org/10.1038/ncomms15840 |
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author | Andersson, Sandra Sundberg, Mårten Pristovsek, Nusa Ibrahim, Ahmed Jonsson, Philip Katona, Borbala Clausson, Carl-Magnus Zieba, Agata Ramström, Margareta Söderberg, Ola Williams, Cecilia Asplund, Anna |
author_facet | Andersson, Sandra Sundberg, Mårten Pristovsek, Nusa Ibrahim, Ahmed Jonsson, Philip Katona, Borbala Clausson, Carl-Magnus Zieba, Agata Ramström, Margareta Söderberg, Ola Williams, Cecilia Asplund, Anna |
author_sort | Andersson, Sandra |
collection | PubMed |
description | The discovery of oestrogen receptor β (ERβ/ESR2) was a landmark discovery. Its reported expression and homology with breast cancer pharmacological target ERα (ESR1) raised hopes for improved endocrine therapies. After 20 years of intense research, this has not materialized. We here perform a rigorous validation of 13 anti-ERβ antibodies, using well-characterized controls and a panel of validation methods. We conclude that only one antibody, the rarely used monoclonal PPZ0506, specifically targets ERβ in immunohistochemistry. Applying this antibody for protein expression profiling in 44 normal and 21 malignant human tissues, we detect ERβ protein in testis, ovary, lymphoid cells, granulosa cell tumours, and a subset of malignant melanoma and thyroid cancers. We do not find evidence of expression in normal or cancerous human breast. This expression pattern aligns well with RNA-seq data, but contradicts a multitude of studies. Our study highlights how inadequately validated antibodies can lead an exciting field astray. |
format | Online Article Text |
id | pubmed-5501969 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-55019692017-07-11 Insufficient antibody validation challenges oestrogen receptor beta research Andersson, Sandra Sundberg, Mårten Pristovsek, Nusa Ibrahim, Ahmed Jonsson, Philip Katona, Borbala Clausson, Carl-Magnus Zieba, Agata Ramström, Margareta Söderberg, Ola Williams, Cecilia Asplund, Anna Nat Commun Article The discovery of oestrogen receptor β (ERβ/ESR2) was a landmark discovery. Its reported expression and homology with breast cancer pharmacological target ERα (ESR1) raised hopes for improved endocrine therapies. After 20 years of intense research, this has not materialized. We here perform a rigorous validation of 13 anti-ERβ antibodies, using well-characterized controls and a panel of validation methods. We conclude that only one antibody, the rarely used monoclonal PPZ0506, specifically targets ERβ in immunohistochemistry. Applying this antibody for protein expression profiling in 44 normal and 21 malignant human tissues, we detect ERβ protein in testis, ovary, lymphoid cells, granulosa cell tumours, and a subset of malignant melanoma and thyroid cancers. We do not find evidence of expression in normal or cancerous human breast. This expression pattern aligns well with RNA-seq data, but contradicts a multitude of studies. Our study highlights how inadequately validated antibodies can lead an exciting field astray. Nature Publishing Group 2017-06-15 /pmc/articles/PMC5501969/ /pubmed/28643774 http://dx.doi.org/10.1038/ncomms15840 Text en Copyright © 2017, The Author(s) http://creativecommons.org/licenses/by/4.0/ Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Andersson, Sandra Sundberg, Mårten Pristovsek, Nusa Ibrahim, Ahmed Jonsson, Philip Katona, Borbala Clausson, Carl-Magnus Zieba, Agata Ramström, Margareta Söderberg, Ola Williams, Cecilia Asplund, Anna Insufficient antibody validation challenges oestrogen receptor beta research |
title | Insufficient antibody validation challenges oestrogen receptor beta research |
title_full | Insufficient antibody validation challenges oestrogen receptor beta research |
title_fullStr | Insufficient antibody validation challenges oestrogen receptor beta research |
title_full_unstemmed | Insufficient antibody validation challenges oestrogen receptor beta research |
title_short | Insufficient antibody validation challenges oestrogen receptor beta research |
title_sort | insufficient antibody validation challenges oestrogen receptor beta research |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5501969/ https://www.ncbi.nlm.nih.gov/pubmed/28643774 http://dx.doi.org/10.1038/ncomms15840 |
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