Downregulation of 15-hydroxyprostaglandin dehydrogenase during acquired tamoxifen resistance and association with poor prognosis in ERα-positive breast cancer

Author:

Volpato Milene1ORCID,Cummings Michele1ORCID,Shaaban Abeer M.2ORCID,Abderrahman Balkees3ORCID,Hull Mark A.1ORCID,Maximov Philipp Y.4,Broom Bradley M.5,Hoppe Reiner6,Fan Ping4,Brauch Hiltrud7ORCID,Jordan V. Craig5ORCID,Speirs Valerie8ORCID

Affiliation:

1. Leeds Institute of Medical Research, University of Leeds, St James’s University Hospital, LS9 7TF Leeds, UK

2. Institute of Cancer and Genomic Sciences, University of Birmingham, B15 2TT Birmingham, UK

3. Leeds Institute of Medical Research, University of Leeds, St James’s University Hospital, LS9 7TF Leeds, UK; Department of Breast Medical Oncology, UT MD Anderson Cancer Center, Houston, TX 77030, USA

4. Department of Breast Medical Oncology, UT MD Anderson Cancer Center, Houston, TX 77030, USA

5. Department of Bioinformatics and Computational Biology, UT MD Anderson Cancer Center, Houston, TX 77030, USA

6. Dr. Margarete Fischer-Bosch Institute of Clinical Pharmacology and University of Tübingen, Auerbachstr. 112, D-70376 Stuttgart, Germany; Germany iFIT Cluster of Excellence, University of Tübingen, Auerbachstr. 112, D-70376 Stuttgart, Germany

7. Dr. Margarete Fischer-Bosch Institute of Clinical Pharmacology and University of Tübingen, Auerbachstr. 112, D-70376 Stuttgart, Germany; Germany iFIT Cluster of Excellence, University of Tübingen, Auerbachstr. 112, D-70376 Stuttgart, Germany; German Cancer Consortium (DKTK) and German Cancer Research Center (DKFZ), Im Neuenheimer Feld 280, 69120 Heidelberg, Germany

8. Leeds Institute of Medical Research, University of Leeds, St James’s University Hospital, LS9 7TF Leeds, UK; Institute of Medical Sciences, University of Aberdeen, Foresterhill, AB25 2ZD Aberdeen, UK

Abstract

Aim: Tamoxifen (TAM) resistance remains a clinical issue in breast cancer. The authors previously reported that 15-hydroxyprostaglandin dehydrogenase (HPGD) was significantly downregulated in tamoxifen-resistant (TAMr) breast cancer cell lines. Here, the authors investigated the relationship between HPGD expression, TAM resistance and prediction of outcome in breast cancer. Methods: HPGD overexpression and silencing studies were performed in isogenic TAMr and parental human breast cancer cell lines to establish the impact of HPGD expression on TAM resistance. HPGD expression and clinical outcome relationships were explored using immunohistochemistry and in silico analysis. Results: Restoration of HPGD expression and activity sensitised TAMr MCF-7 cells to TAM and 17β-oestradiol, whilst HPGD silencing in parental MCF-7 cells reduced TAM sensitivity. TAMr cells released more prostaglandin E2 (PGE2) than controls, which was reduced in TAMr cells stably transfected with HPGD. Exogenous PGE2 signalled through the EP4 receptor to reduce breast cancer cell sensitivity to TAM. Decreased HPGD expression was associated with decreased overall survival in ERα-positive breast cancer patients. Conclusions: HPGD downregulation in breast cancer is associated with reduced response to TAM therapy via PGE2-EP4 signalling and decreases patient survival. The data offer a potential target to develop combination therapies that may overcome acquired tamoxifen resistance.

Funder

Cancer Research UK

Yorkshire Cancer Research

Robert Bosch Stiftung

National Institutes of Health

University of Texas MD Anderson Cancer Center

Publisher

Open Exploration Publishing

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