The potential role of collagen type VII in breast cancer proliferation.

Breast cancer Collagen type VII Extracellular matrix Mesenchymal stem cell

Journal

Cancer cell international
ISSN: 1475-2867
Titre abrégé: Cancer Cell Int
Pays: England
ID NLM: 101139795

Informations de publication

Date de publication:
20 Jul 2024
Historique:
received: 22 04 2024
accepted: 12 07 2024
medline: 20 7 2024
pubmed: 20 7 2024
entrez: 19 7 2024
Statut: epublish

Résumé

Breast cancer is the most common cancer in women. Cancer cells can persist in a prolonged dormant state for years without any clinical evidence of disease creating an urgent need to better understand the molecular mechanisms leading to relapse. This study aimed to identify extracellular matrix (ECM) components associated with hypoxia-induced breast cancer dormancy. The effects of selected ECM proteins on breast cancer cell proliferation were analyzed, along with their correlation with established prognostic markers in human breast cancer tissue. Screening of extracellular matrix proteins was performed in hypoxia-induced dormant MCF-7 breast cancer cells. Proliferation of MCF-7 cells in vitro was subsequently determined in the presence of recombinant ColVII. Adipose tissue-derived mesenchymal stem cells (AdMSCs) subpopulation overexpressing ColVII were indirectly isolated by ColVII receptor integrin-α6 specific antibodies. AdMSCs- MCF-7 3D spheroid cultures were generated to model solid tumour conditions. In addition, the association between ColVII and various prognostic markers was evaluated in clinical samples of human breast cancer tissue. Dormant MCF-7 cells showed an elevated expression of ColVII while MCF-7 cells cultured on ColVII exhibited reduced proliferation in vitro. In AdMSCs-MCF-7 3D spheroids, a reduced proliferation of MCF-7 cells was observed in Int-α6 ColVII is associated with reduced proliferation of breast cancer cells in vitro. ColVII is strongly expressed in myoepithelial cells and in breast cancer tissue the high ColVII expression correlates with several well-known positive prognostic markers, highlighting its potential as a prognostic marker in breast cancer.

Sections du résumé

BACKGROUND BACKGROUND
Breast cancer is the most common cancer in women. Cancer cells can persist in a prolonged dormant state for years without any clinical evidence of disease creating an urgent need to better understand the molecular mechanisms leading to relapse. This study aimed to identify extracellular matrix (ECM) components associated with hypoxia-induced breast cancer dormancy. The effects of selected ECM proteins on breast cancer cell proliferation were analyzed, along with their correlation with established prognostic markers in human breast cancer tissue.
MATERIALS AND METHODS METHODS
Screening of extracellular matrix proteins was performed in hypoxia-induced dormant MCF-7 breast cancer cells. Proliferation of MCF-7 cells in vitro was subsequently determined in the presence of recombinant ColVII. Adipose tissue-derived mesenchymal stem cells (AdMSCs) subpopulation overexpressing ColVII were indirectly isolated by ColVII receptor integrin-α6 specific antibodies. AdMSCs- MCF-7 3D spheroid cultures were generated to model solid tumour conditions. In addition, the association between ColVII and various prognostic markers was evaluated in clinical samples of human breast cancer tissue.
RESULTS RESULTS
Dormant MCF-7 cells showed an elevated expression of ColVII while MCF-7 cells cultured on ColVII exhibited reduced proliferation in vitro. In AdMSCs-MCF-7 3D spheroids, a reduced proliferation of MCF-7 cells was observed in Int-α6
CONCLUSION CONCLUSIONS
ColVII is associated with reduced proliferation of breast cancer cells in vitro. ColVII is strongly expressed in myoepithelial cells and in breast cancer tissue the high ColVII expression correlates with several well-known positive prognostic markers, highlighting its potential as a prognostic marker in breast cancer.

Identifiants

pubmed: 39030607
doi: 10.1186/s12935-024-03449-4
pii: 10.1186/s12935-024-03449-4
doi:

Types de publication

Journal Article

Langues

eng

Pagination

254

Informations de copyright

© 2024. The Author(s).

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Auteurs

Sergio Pérez-Díaz (S)

Department of Medical and Translational Biology, Umeå University, Umeå, SE-901 87, Sweden. sergio.perez.diaz@ki.se.
Department of Laboratory Medicine, Division of Clinical Physiology, Karolinska Institute, Stockholm, Sweden. sergio.perez.diaz@ki.se.

Jessica Lindberg (J)

Department of Medical and Translational Biology, Umeå University, Umeå, SE-901 87, Sweden.
Department of Diagnostics and Intervention, Plastic Surgery and Surgery, Umeå University, Umeå, Sweden.

Luis Oliveros Anerillas (LO)

Department of Medical and Translational Biology, Umeå University, Umeå, SE-901 87, Sweden.

Paul J Kingham (PJ)

Department of Medical and Translational Biology, Umeå University, Umeå, SE-901 87, Sweden.

Malin Sund (M)

Department of Diagnostics and Intervention, Plastic Surgery and Surgery, Umeå University, Umeå, Sweden.
Department of Surgery/CLINICUM, University of Helsinki and Helsinki University Hospital, Helsinki, Finland.

Gunilla Rask (G)

Department of Diagnostics and Intervention, Plastic Surgery and Surgery, Umeå University, Umeå, Sweden.

Johan Svensson (J)

Department of Statistics, Umeå School of Business, Economics and Statistics, Umeå University, Umeå, Sweden.

Malin Jansson (M)

Department of Diagnostics and Intervention, Plastic Surgery and Surgery, Umeå University, Umeå, Sweden.

Rebecca Wiberg (R)

Department of Medical and Translational Biology, Umeå University, Umeå, SE-901 87, Sweden.
Department of Diagnostics and Intervention, Plastic Surgery and Surgery, Umeå University, Umeå, Sweden.

Classifications MeSH