Mechanostimulation of breast myoepithelial cells induces functional changes associated with DCIS progression to invasion

Abstract Women with ductal carcinoma in situ (DCIS) have an increased risk of progression to invasive breast cancer. Although not all women with DCIS will progress to invasion, all are treated as such, emphasising the need to identify prognostic biomarkers. We have previously shown that altered myoe...

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Main Authors: Mary-Kate Hayward, Michael D. Allen, Jennifer J. Gomm, Iain Goulding, Clare L. Thompson, Martin M. Knight, John F. Marshall, J. Louise Jones
Format: Article
Language:English
Published: Nature Portfolio 2022-09-01
Series:npj Breast Cancer
Online Access:https://doi.org/10.1038/s41523-022-00464-4
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author Mary-Kate Hayward
Michael D. Allen
Jennifer J. Gomm
Iain Goulding
Clare L. Thompson
Martin M. Knight
John F. Marshall
J. Louise Jones
author_facet Mary-Kate Hayward
Michael D. Allen
Jennifer J. Gomm
Iain Goulding
Clare L. Thompson
Martin M. Knight
John F. Marshall
J. Louise Jones
author_sort Mary-Kate Hayward
collection DOAJ
description Abstract Women with ductal carcinoma in situ (DCIS) have an increased risk of progression to invasive breast cancer. Although not all women with DCIS will progress to invasion, all are treated as such, emphasising the need to identify prognostic biomarkers. We have previously shown that altered myoepithelial cells in DCIS predict disease progression and recurrence. By analysing DCIS duct size in sections of human breast tumour samples, we identified an associated upregulation of integrin β6 and an increase in periductal fibronectin deposition with increased DCIS duct size that associated with the progression of DCIS to invasion. Our modelling of the mechanical stretching myoepithelial cells undergo during DCIS progression confirmed the upregulation of integrin β6 and fibronectin expression in isolated primary and cell line models of normal myoepithelial cells. Our studies reveal that this mechanostimulated DCIS myoepithelial cell phenotype enhances invasion in a TGFβ-mediated upregulation of MMP13. Immunohistochemical analysis identified that MMP13 was specifically upregulated in DCIS, and it was associated with progression to invasion. These findings implicate tissue mechanics in altering the myoepithelial cell phenotype in DCIS, and that these alterations may be used to stratify DCIS patients into low and high risk for invasive progression.
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spelling doaj.art-df3865fd8d414597839305295fcc1d882023-11-02T05:20:49ZengNature Portfolionpj Breast Cancer2374-46772022-09-018111210.1038/s41523-022-00464-4Mechanostimulation of breast myoepithelial cells induces functional changes associated with DCIS progression to invasionMary-Kate Hayward0Michael D. Allen1Jennifer J. Gomm2Iain Goulding3Clare L. Thompson4Martin M. Knight5John F. Marshall6J. Louise Jones7Centre for Tumour Biology, Barts Cancer Institute, Queen Mary University of London, John Vane Science CentreCentre for Tumour Biology, Barts Cancer Institute, Queen Mary University of London, John Vane Science CentreCentre for Tumour Biology, Barts Cancer Institute, Queen Mary University of London, John Vane Science CentreCentre for Tumour Biology, Barts Cancer Institute, Queen Mary University of London, John Vane Science CentreSchool of Engineering and Materials Science, Queen Mary University of LondonSchool of Engineering and Materials Science, Queen Mary University of LondonCentre for Tumour Biology, Barts Cancer Institute, Queen Mary University of London, John Vane Science CentreCentre for Tumour Biology, Barts Cancer Institute, Queen Mary University of London, John Vane Science CentreAbstract Women with ductal carcinoma in situ (DCIS) have an increased risk of progression to invasive breast cancer. Although not all women with DCIS will progress to invasion, all are treated as such, emphasising the need to identify prognostic biomarkers. We have previously shown that altered myoepithelial cells in DCIS predict disease progression and recurrence. By analysing DCIS duct size in sections of human breast tumour samples, we identified an associated upregulation of integrin β6 and an increase in periductal fibronectin deposition with increased DCIS duct size that associated with the progression of DCIS to invasion. Our modelling of the mechanical stretching myoepithelial cells undergo during DCIS progression confirmed the upregulation of integrin β6 and fibronectin expression in isolated primary and cell line models of normal myoepithelial cells. Our studies reveal that this mechanostimulated DCIS myoepithelial cell phenotype enhances invasion in a TGFβ-mediated upregulation of MMP13. Immunohistochemical analysis identified that MMP13 was specifically upregulated in DCIS, and it was associated with progression to invasion. These findings implicate tissue mechanics in altering the myoepithelial cell phenotype in DCIS, and that these alterations may be used to stratify DCIS patients into low and high risk for invasive progression.https://doi.org/10.1038/s41523-022-00464-4
spellingShingle Mary-Kate Hayward
Michael D. Allen
Jennifer J. Gomm
Iain Goulding
Clare L. Thompson
Martin M. Knight
John F. Marshall
J. Louise Jones
Mechanostimulation of breast myoepithelial cells induces functional changes associated with DCIS progression to invasion
npj Breast Cancer
title Mechanostimulation of breast myoepithelial cells induces functional changes associated with DCIS progression to invasion
title_full Mechanostimulation of breast myoepithelial cells induces functional changes associated with DCIS progression to invasion
title_fullStr Mechanostimulation of breast myoepithelial cells induces functional changes associated with DCIS progression to invasion
title_full_unstemmed Mechanostimulation of breast myoepithelial cells induces functional changes associated with DCIS progression to invasion
title_short Mechanostimulation of breast myoepithelial cells induces functional changes associated with DCIS progression to invasion
title_sort mechanostimulation of breast myoepithelial cells induces functional changes associated with dcis progression to invasion
url https://doi.org/10.1038/s41523-022-00464-4
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