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Evaluation of SPP1/osteopontin expression as predictor of recurrence in tamoxifen treated breast cancer
Breast cancer patients treated with tamoxifen may experience recurrence due to endocrine resistance, which highlights the need for additional predictive and prognostic biomarkers. The glyco-phosphoprotein osteopontin (OPN), encoded by the SPP1 gene, has previously shown to be associated with poor pr...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6989629/ https://www.ncbi.nlm.nih.gov/pubmed/31996744 http://dx.doi.org/10.1038/s41598-020-58323-w |
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author | Göthlin Eremo, Anna Lagergren, Kajsa Othman, Lana Montgomery, Scott Andersson, Göran Tina, Elisabet |
author_facet | Göthlin Eremo, Anna Lagergren, Kajsa Othman, Lana Montgomery, Scott Andersson, Göran Tina, Elisabet |
author_sort | Göthlin Eremo, Anna |
collection | PubMed |
description | Breast cancer patients treated with tamoxifen may experience recurrence due to endocrine resistance, which highlights the need for additional predictive and prognostic biomarkers. The glyco-phosphoprotein osteopontin (OPN), encoded by the SPP1 gene, has previously shown to be associated with poor prognosis in breast cancer. However, studies on the predictive value of OPN are inconclusive. In the present study, we evaluated tissue SPP1 mRNA and OPN protein expression as markers of recurrence in estrogen receptor- positive (ER+) breast cancer tissue. Tamoxifen- treated patients with recurrence or non-recurrence were selected using a matched case-control design. SPP1 mRNA expression was analysed using qPCR (n = 100) and OPN protein by immunohistochemistry (n = 116) using different antibodies. Odds ratios were estimated with conditional logistic regression. The SPP1 expression increased the risk of recurrence with an odds ratio (OR) of 2.50 (95% confidence interval [CI]; 1.30–4.82), after adjustment for tumour grade, HER 2 status and other treatments to OR 3.62 (95% CI; 1.45–9.07). However, OPN protein expression was not associated with risk of recurrence or with SPP1-gene expression, suggesting SPP1 mRNA a stronger prognostic marker candidate compared to tumor tissue OPN protein. |
format | Online Article Text |
id | pubmed-6989629 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-69896292020-02-05 Evaluation of SPP1/osteopontin expression as predictor of recurrence in tamoxifen treated breast cancer Göthlin Eremo, Anna Lagergren, Kajsa Othman, Lana Montgomery, Scott Andersson, Göran Tina, Elisabet Sci Rep Article Breast cancer patients treated with tamoxifen may experience recurrence due to endocrine resistance, which highlights the need for additional predictive and prognostic biomarkers. The glyco-phosphoprotein osteopontin (OPN), encoded by the SPP1 gene, has previously shown to be associated with poor prognosis in breast cancer. However, studies on the predictive value of OPN are inconclusive. In the present study, we evaluated tissue SPP1 mRNA and OPN protein expression as markers of recurrence in estrogen receptor- positive (ER+) breast cancer tissue. Tamoxifen- treated patients with recurrence or non-recurrence were selected using a matched case-control design. SPP1 mRNA expression was analysed using qPCR (n = 100) and OPN protein by immunohistochemistry (n = 116) using different antibodies. Odds ratios were estimated with conditional logistic regression. The SPP1 expression increased the risk of recurrence with an odds ratio (OR) of 2.50 (95% confidence interval [CI]; 1.30–4.82), after adjustment for tumour grade, HER 2 status and other treatments to OR 3.62 (95% CI; 1.45–9.07). However, OPN protein expression was not associated with risk of recurrence or with SPP1-gene expression, suggesting SPP1 mRNA a stronger prognostic marker candidate compared to tumor tissue OPN protein. Nature Publishing Group UK 2020-01-29 /pmc/articles/PMC6989629/ /pubmed/31996744 http://dx.doi.org/10.1038/s41598-020-58323-w Text en © The Author(s) 2020 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 Göthlin Eremo, Anna Lagergren, Kajsa Othman, Lana Montgomery, Scott Andersson, Göran Tina, Elisabet Evaluation of SPP1/osteopontin expression as predictor of recurrence in tamoxifen treated breast cancer |
title | Evaluation of SPP1/osteopontin expression as predictor of recurrence in tamoxifen treated breast cancer |
title_full | Evaluation of SPP1/osteopontin expression as predictor of recurrence in tamoxifen treated breast cancer |
title_fullStr | Evaluation of SPP1/osteopontin expression as predictor of recurrence in tamoxifen treated breast cancer |
title_full_unstemmed | Evaluation of SPP1/osteopontin expression as predictor of recurrence in tamoxifen treated breast cancer |
title_short | Evaluation of SPP1/osteopontin expression as predictor of recurrence in tamoxifen treated breast cancer |
title_sort | evaluation of spp1/osteopontin expression as predictor of recurrence in tamoxifen treated breast cancer |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6989629/ https://www.ncbi.nlm.nih.gov/pubmed/31996744 http://dx.doi.org/10.1038/s41598-020-58323-w |
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