Type IV collagen as a potential biomarker of metastatic breast cancer.


Journal

Clinical & experimental metastasis
ISSN: 1573-7276
Titre abrégé: Clin Exp Metastasis
Pays: Netherlands
ID NLM: 8409970

Informations de publication

Date de publication:
04 2021
Historique:
received: 03 12 2020
accepted: 15 02 2021
pubmed: 4 3 2021
medline: 28 7 2021
entrez: 3 3 2021
Statut: ppublish

Résumé

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.

Identifiants

pubmed: 33655422
doi: 10.1007/s10585-021-10082-2
pii: 10.1007/s10585-021-10082-2
pmc: PMC7987628
doi:

Substances chimiques

Biomarkers, Tumor 0
Collagen Type IV 0
MUC1 protein, human 0
Mucin-1 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

175-185

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Auteurs

Moa Lindgren (M)

Department of Surgery, Department of Surgical and Perioperative Sciences, Umeå University, By 10A, Norrlands Universitetssjukhus, Umeå, 901 85, Sweden.

Malin Jansson (M)

Department of Surgery, Department of Surgical and Perioperative Sciences, Umeå University, By 10A, Norrlands Universitetssjukhus, Umeå, 901 85, Sweden.

Björn Tavelin (B)

Department of Radiation Sciences, Umeå University, Umeå, Sweden.

Luc Dirix (L)

Translational Cancer Research Unit, GZA Hospital Sint Augustinus and Antwerp University, Antwerp, Belgium.

Peter Vermeulen (P)

Translational Cancer Research Unit, GZA Hospital Sint Augustinus and Antwerp University, Antwerp, Belgium.

Hanna Nyström (H)

Department of Surgery, Department of Surgical and Perioperative Sciences, Umeå University, By 10A, Norrlands Universitetssjukhus, Umeå, 901 85, Sweden. hanna.nystrom@umu.se.
Translational Cancer Research Unit, GZA Hospital Sint Augustinus and Antwerp University, Antwerp, Belgium. hanna.nystrom@umu.se.
Wallenberg Centre for Molecular Medicine, Umeå University, Umeå, Sweden. hanna.nystrom@umu.se.

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