Insufficient antibody validation challenges oestrogen receptor beta research

Sandra Andersson(Uppsala University), Mårten Sundberg(Uppsala University), Nuša Pristovšek(Uppsala University), Ahmed Atef Ibrahim(Science for Life Laboratory), Philip Jonsson(University of Houston), Borbala Katona(Uppsala University), Carl-Magnus Clausson(Uppsala University), Agata Zieba(Uppsala University), Margareta Ramström(Uppsala University), Ola Söderberg(Uppsala University), Cecilia Williams(Science for Life Laboratory), Anna Asplund(Uppsala University)
Nature Communications
June 15, 2017
Cited by 252Open Access
Full Text

Abstract

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.


Related Papers

No related papers found

Powered by citation graph analysis