Cargando…
Type IV collagen as a potential biomarker of metastatic breast cancer
No reliable, non-invasive biomarker of metastatic breast cancer (mBC) exists: circulating CA15-3 (cCA15-3) is the marker mostly used to monitor mBC. Circulating collagen IV (cCOLIV) has been evaluated in other metastatic cancers and has been found to be a promising biomarker. The overarching aim of...
Autores principales: | , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Netherlands
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7987628/ https://www.ncbi.nlm.nih.gov/pubmed/33655422 http://dx.doi.org/10.1007/s10585-021-10082-2 |
_version_ | 1783668650601873408 |
---|---|
author | Lindgren, Moa Jansson, Malin Tavelin, Björn Dirix, Luc Vermeulen, Peter Nyström, Hanna |
author_facet | Lindgren, Moa Jansson, Malin Tavelin, Björn Dirix, Luc Vermeulen, Peter Nyström, Hanna |
author_sort | Lindgren, Moa |
collection | PubMed |
description | No reliable, non-invasive biomarker of metastatic breast cancer (mBC) exists: circulating CA15-3 (cCA15-3) is the marker mostly used to monitor mBC. Circulating collagen IV (cCOLIV) has been evaluated in other metastatic cancers and has been found to be a promising biomarker. The overarching aim of this study was to evaluate cCOLIV as a potential biomarker in patients with mBC. The first aim was to determine the levels of cCOL IV and cCA15-3 in patients with healthy controls, primary breast cancer (pBC) and mBC. The second aim was to compare levels of cCOLIV and cCA15-3 in patients with different metastatic sites of BC. The third aim was to investigate the prognostic value of cCOLIV and cCA15-3 for mBC patients. The fourth aim was to analyse whether a combination of the two biomarkers was more accurate in detecting mBC than a single marker. Lastly, we investigated the tissue expression levels of COLIV in BC bone metastases (BM) and liver metastases (LM). Plasma levels of cCOLIV and cCA15-3 from healthy controls and patients with pBC and mBC were measured. COLIV expression in tissue from patients with LM and BM was analysed using immunohistochemistry. Clinical and survival data were collected from medical charts. The levels of cCOLIV and cCA15-3 were significantly elevated in mBC patients compared with healthy controls and pBC patients. No differences in cCOLIV and cCA15-3 levels were found based on the metastatic site. High levels of cCOLIV, but not cCA15-3, correlated with poorer survival. cCOLIV alone and the combination of cCA15-3 and cCOLIV were superior to cCA15-3 at detecting mBC. COL IV was highly expressed in the tissue of LM and BM. Our study suggests that cCOLIV is a potential marker to monitor patients with BC. SUPPLEMENTARY INFORMATION: The online version of this article (10.1007/s10585-021-10082-2) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-7987628 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Springer Netherlands |
record_format | MEDLINE/PubMed |
spelling | pubmed-79876282021-04-12 Type IV collagen as a potential biomarker of metastatic breast cancer Lindgren, Moa Jansson, Malin Tavelin, Björn Dirix, Luc Vermeulen, Peter Nyström, Hanna Clin Exp Metastasis Research Paper No reliable, non-invasive biomarker of metastatic breast cancer (mBC) exists: circulating CA15-3 (cCA15-3) is the marker mostly used to monitor mBC. Circulating collagen IV (cCOLIV) has been evaluated in other metastatic cancers and has been found to be a promising biomarker. The overarching aim of this study was to evaluate cCOLIV as a potential biomarker in patients with mBC. The first aim was to determine the levels of cCOL IV and cCA15-3 in patients with healthy controls, primary breast cancer (pBC) and mBC. The second aim was to compare levels of cCOLIV and cCA15-3 in patients with different metastatic sites of BC. The third aim was to investigate the prognostic value of cCOLIV and cCA15-3 for mBC patients. The fourth aim was to analyse whether a combination of the two biomarkers was more accurate in detecting mBC than a single marker. Lastly, we investigated the tissue expression levels of COLIV in BC bone metastases (BM) and liver metastases (LM). Plasma levels of cCOLIV and cCA15-3 from healthy controls and patients with pBC and mBC were measured. COLIV expression in tissue from patients with LM and BM was analysed using immunohistochemistry. Clinical and survival data were collected from medical charts. The levels of cCOLIV and cCA15-3 were significantly elevated in mBC patients compared with healthy controls and pBC patients. No differences in cCOLIV and cCA15-3 levels were found based on the metastatic site. High levels of cCOLIV, but not cCA15-3, correlated with poorer survival. cCOLIV alone and the combination of cCA15-3 and cCOLIV were superior to cCA15-3 at detecting mBC. COL IV was highly expressed in the tissue of LM and BM. Our study suggests that cCOLIV is a potential marker to monitor patients with BC. SUPPLEMENTARY INFORMATION: The online version of this article (10.1007/s10585-021-10082-2) contains supplementary material, which is available to authorized users. Springer Netherlands 2021-03-03 2021 /pmc/articles/PMC7987628/ /pubmed/33655422 http://dx.doi.org/10.1007/s10585-021-10082-2 Text en © The Author(s) 2021 Open AccessThis 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Research Paper Lindgren, Moa Jansson, Malin Tavelin, Björn Dirix, Luc Vermeulen, Peter Nyström, Hanna Type IV collagen as a potential biomarker of metastatic breast cancer |
title | Type IV collagen as a potential biomarker of metastatic breast cancer |
title_full | Type IV collagen as a potential biomarker of metastatic breast cancer |
title_fullStr | Type IV collagen as a potential biomarker of metastatic breast cancer |
title_full_unstemmed | Type IV collagen as a potential biomarker of metastatic breast cancer |
title_short | Type IV collagen as a potential biomarker of metastatic breast cancer |
title_sort | type iv collagen as a potential biomarker of metastatic breast cancer |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7987628/ https://www.ncbi.nlm.nih.gov/pubmed/33655422 http://dx.doi.org/10.1007/s10585-021-10082-2 |
work_keys_str_mv | AT lindgrenmoa typeivcollagenasapotentialbiomarkerofmetastaticbreastcancer AT janssonmalin typeivcollagenasapotentialbiomarkerofmetastaticbreastcancer AT tavelinbjorn typeivcollagenasapotentialbiomarkerofmetastaticbreastcancer AT dirixluc typeivcollagenasapotentialbiomarkerofmetastaticbreastcancer AT vermeulenpeter typeivcollagenasapotentialbiomarkerofmetastaticbreastcancer AT nystromhanna typeivcollagenasapotentialbiomarkerofmetastaticbreastcancer |