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Dysregulated EGFR pathway in serum in early-stage breast cancer patients: A case control study
The epidermal growth factor receptor (EGFR) and its ligands are involved in cancer pathogenesis and they might serve as circulating biomarkers. The current study aims to investigate if abnormal pre-treatment serum levels of EGFR and EGFR ligands are present in women with early-stage breast cancer an...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7174424/ https://www.ncbi.nlm.nih.gov/pubmed/32317675 http://dx.doi.org/10.1038/s41598-020-63375-z |
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author | Kjær, Ina Mathilde Olsen, Dorte Aalund Brandslund, Ivan Bechmann, Troels Jakobsen, Erik Hugger Bogh, Søren Bie Madsen, Jonna Skov |
author_facet | Kjær, Ina Mathilde Olsen, Dorte Aalund Brandslund, Ivan Bechmann, Troels Jakobsen, Erik Hugger Bogh, Søren Bie Madsen, Jonna Skov |
author_sort | Kjær, Ina Mathilde |
collection | PubMed |
description | The epidermal growth factor receptor (EGFR) and its ligands are involved in cancer pathogenesis and they might serve as circulating biomarkers. The current study aims to investigate if abnormal pre-treatment serum levels of EGFR and EGFR ligands are present in women with early-stage breast cancer and if up- or downregulation of EGFR and EGFR ligands occur in defined patient subgroups. Pre-treatment serum samples were obtained from 311 women with newly diagnosed early-stage breast cancer and from 419 healthy women and analysed for EGFR and the ligands: Epidermal growth factor (EGF), heparin-binding epidermal growth factor (HBEGF), betacellulin (BTC), amphiregulin (AREG), and transforming growth factor α (TGF-α). Previously, age-dependent 95% reference intervals for EGFR and the EGFR ligands have been established based on the healthy women population. S-EGFR, S-EGF, S-HBEGF, S-AREG, and S-TGFα were all significantly different in women with breast cancer compared to healthy women (p < 0.05). Elevated S-EGFR, according to the reference intervals, was present in 11.3% of breast cancer patients, whereas decreased S-EGF was found in 11.6%. Elevated S-EGFR was associated with estrogen receptor positivity of tumor (ER+) and a subgroup of ER + breast cancer patients showed markedly elevated S-EGFR (>120 ng/mL). |
format | Online Article Text |
id | pubmed-7174424 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-71744242020-04-24 Dysregulated EGFR pathway in serum in early-stage breast cancer patients: A case control study Kjær, Ina Mathilde Olsen, Dorte Aalund Brandslund, Ivan Bechmann, Troels Jakobsen, Erik Hugger Bogh, Søren Bie Madsen, Jonna Skov Sci Rep Article The epidermal growth factor receptor (EGFR) and its ligands are involved in cancer pathogenesis and they might serve as circulating biomarkers. The current study aims to investigate if abnormal pre-treatment serum levels of EGFR and EGFR ligands are present in women with early-stage breast cancer and if up- or downregulation of EGFR and EGFR ligands occur in defined patient subgroups. Pre-treatment serum samples were obtained from 311 women with newly diagnosed early-stage breast cancer and from 419 healthy women and analysed for EGFR and the ligands: Epidermal growth factor (EGF), heparin-binding epidermal growth factor (HBEGF), betacellulin (BTC), amphiregulin (AREG), and transforming growth factor α (TGF-α). Previously, age-dependent 95% reference intervals for EGFR and the EGFR ligands have been established based on the healthy women population. S-EGFR, S-EGF, S-HBEGF, S-AREG, and S-TGFα were all significantly different in women with breast cancer compared to healthy women (p < 0.05). Elevated S-EGFR, according to the reference intervals, was present in 11.3% of breast cancer patients, whereas decreased S-EGF was found in 11.6%. Elevated S-EGFR was associated with estrogen receptor positivity of tumor (ER+) and a subgroup of ER + breast cancer patients showed markedly elevated S-EGFR (>120 ng/mL). Nature Publishing Group UK 2020-04-21 /pmc/articles/PMC7174424/ /pubmed/32317675 http://dx.doi.org/10.1038/s41598-020-63375-z 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 Kjær, Ina Mathilde Olsen, Dorte Aalund Brandslund, Ivan Bechmann, Troels Jakobsen, Erik Hugger Bogh, Søren Bie Madsen, Jonna Skov Dysregulated EGFR pathway in serum in early-stage breast cancer patients: A case control study |
title | Dysregulated EGFR pathway in serum in early-stage breast cancer patients: A case control study |
title_full | Dysregulated EGFR pathway in serum in early-stage breast cancer patients: A case control study |
title_fullStr | Dysregulated EGFR pathway in serum in early-stage breast cancer patients: A case control study |
title_full_unstemmed | Dysregulated EGFR pathway in serum in early-stage breast cancer patients: A case control study |
title_short | Dysregulated EGFR pathway in serum in early-stage breast cancer patients: A case control study |
title_sort | dysregulated egfr pathway in serum in early-stage breast cancer patients: a case control study |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7174424/ https://www.ncbi.nlm.nih.gov/pubmed/32317675 http://dx.doi.org/10.1038/s41598-020-63375-z |
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