Mechanical Stimulation Modulates Osteocyte Regulation of Cancer Cell Phenotype

Breast and prostate cancers preferentially metastasise to bone tissue, with metastatic lesions forming in the skeletons of most patients. On arriving in bone tissue, disseminated tumour cells enter a mechanical microenvironment that is substantially different to that of the primary tumour and is lar...

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Main Authors: Stefaan W. Verbruggen, Clare L. Thompson, Michael P. Duffy, Sophia Lunetto, Joanne Nolan, Oliver M. T. Pearce, Christopher R. Jacobs, Martin M. Knight
Format: Article
Language:English
Published: MDPI AG 2021-06-01
Series:Cancers
Subjects:
Online Access:https://www.mdpi.com/2072-6694/13/12/2906
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spelling doaj-ab4d4dfee0f14351b4f8bf270bc9f4062021-06-30T23:50:52ZengMDPI AGCancers2072-66942021-06-01132906290610.3390/cancers13122906Mechanical Stimulation Modulates Osteocyte Regulation of Cancer Cell PhenotypeStefaan W. Verbruggen0Clare L. Thompson1Michael P. Duffy2Sophia Lunetto3Joanne Nolan4Oliver M. T. Pearce5Christopher R. Jacobs6Martin M. Knight7Department of Biomedical Engineering, Columbia University in the City of New York, New York, NY 10027, USACentre for Predictive in vitro Models, School of Engineering and Materials Science, Queen Mary University of London, London E1 4NS, UKDepartment of Biomedical Engineering, Columbia University in the City of New York, New York, NY 10027, USACentre for Predictive in vitro Models, School of Engineering and Materials Science, Queen Mary University of London, London E1 4NS, UKCentre for Predictive in vitro Models, School of Engineering and Materials Science, Queen Mary University of London, London E1 4NS, UKBarts Cancer Institute, School of Medicine and Dentistry, Queen Mary University of London, London EC1M 5PZ, UKDepartment of Biomedical Engineering, Columbia University in the City of New York, New York, NY 10027, USACentre for Predictive in vitro Models, School of Engineering and Materials Science, Queen Mary University of London, London E1 4NS, UKBreast and prostate cancers preferentially metastasise to bone tissue, with metastatic lesions forming in the skeletons of most patients. On arriving in bone tissue, disseminated tumour cells enter a mechanical microenvironment that is substantially different to that of the primary tumour and is largely regulated by bone cells. Osteocytes, the most ubiquitous bone cell type, orchestrate healthy bone remodelling in response to physical exercise. However, the effects of mechanical loading of osteocytes on cancer cell behaviour is still poorly understood. The aim of this study was to characterise the effects of osteocyte mechanical stimulation on the behaviour of breast and prostate cancer cells. To replicate an osteocyte-controlled environment, this study treated breast (MDA-MB-231 and MCF-7) and prostate (PC-3 and LNCaP) cancer cell lines with conditioned media from MLO-Y4 osteocyte-like cells exposed to mechanical stimulation in the form of fluid shear stress. We found that osteocyte paracrine signalling acted to inhibit metastatic breast and prostate tumour growth, characterised by reduced proliferation and invasion and increased migration. In breast cancer cells, these effects were largely reversed by mechanical stimulation of osteocytes. In contrast, conditioned media from mechanically stimulated osteocytes had no effect on prostate cancer cells. To further investigate these interactions, we developed a microfluidic organ-chip model using the Emulate platform. This new organ-chip model enabled analysis of cancer cell migration, proliferation and invasion in the presence of mechanical stimulation of osteocytes by fluid shear stress, resulting in increased invasion of breast and prostate cancer cells. These findings demonstrate the importance of osteocytes and mechanical loading in regulating cancer cell behaviour and the need to incorporate these factors into predictive in vitro models of bone metastasis.https://www.mdpi.com/2072-6694/13/12/2906breast cancerprostate cancertumour metastasisbone metastatic diseasecell co-culturemechanical stimulation
collection DOAJ
language English
format Article
sources DOAJ
author Stefaan W. Verbruggen
Clare L. Thompson
Michael P. Duffy
Sophia Lunetto
Joanne Nolan
Oliver M. T. Pearce
Christopher R. Jacobs
Martin M. Knight
spellingShingle Stefaan W. Verbruggen
Clare L. Thompson
Michael P. Duffy
Sophia Lunetto
Joanne Nolan
Oliver M. T. Pearce
Christopher R. Jacobs
Martin M. Knight
Mechanical Stimulation Modulates Osteocyte Regulation of Cancer Cell Phenotype
Cancers
breast cancer
prostate cancer
tumour metastasis
bone metastatic disease
cell co-culture
mechanical stimulation
author_facet Stefaan W. Verbruggen
Clare L. Thompson
Michael P. Duffy
Sophia Lunetto
Joanne Nolan
Oliver M. T. Pearce
Christopher R. Jacobs
Martin M. Knight
author_sort Stefaan W. Verbruggen
title Mechanical Stimulation Modulates Osteocyte Regulation of Cancer Cell Phenotype
title_short Mechanical Stimulation Modulates Osteocyte Regulation of Cancer Cell Phenotype
title_full Mechanical Stimulation Modulates Osteocyte Regulation of Cancer Cell Phenotype
title_fullStr Mechanical Stimulation Modulates Osteocyte Regulation of Cancer Cell Phenotype
title_full_unstemmed Mechanical Stimulation Modulates Osteocyte Regulation of Cancer Cell Phenotype
title_sort mechanical stimulation modulates osteocyte regulation of cancer cell phenotype
publisher MDPI AG
series Cancers
issn 2072-6694
publishDate 2021-06-01
description Breast and prostate cancers preferentially metastasise to bone tissue, with metastatic lesions forming in the skeletons of most patients. On arriving in bone tissue, disseminated tumour cells enter a mechanical microenvironment that is substantially different to that of the primary tumour and is largely regulated by bone cells. Osteocytes, the most ubiquitous bone cell type, orchestrate healthy bone remodelling in response to physical exercise. However, the effects of mechanical loading of osteocytes on cancer cell behaviour is still poorly understood. The aim of this study was to characterise the effects of osteocyte mechanical stimulation on the behaviour of breast and prostate cancer cells. To replicate an osteocyte-controlled environment, this study treated breast (MDA-MB-231 and MCF-7) and prostate (PC-3 and LNCaP) cancer cell lines with conditioned media from MLO-Y4 osteocyte-like cells exposed to mechanical stimulation in the form of fluid shear stress. We found that osteocyte paracrine signalling acted to inhibit metastatic breast and prostate tumour growth, characterised by reduced proliferation and invasion and increased migration. In breast cancer cells, these effects were largely reversed by mechanical stimulation of osteocytes. In contrast, conditioned media from mechanically stimulated osteocytes had no effect on prostate cancer cells. To further investigate these interactions, we developed a microfluidic organ-chip model using the Emulate platform. This new organ-chip model enabled analysis of cancer cell migration, proliferation and invasion in the presence of mechanical stimulation of osteocytes by fluid shear stress, resulting in increased invasion of breast and prostate cancer cells. These findings demonstrate the importance of osteocytes and mechanical loading in regulating cancer cell behaviour and the need to incorporate these factors into predictive in vitro models of bone metastasis.
topic breast cancer
prostate cancer
tumour metastasis
bone metastatic disease
cell co-culture
mechanical stimulation
url https://www.mdpi.com/2072-6694/13/12/2906
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