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Development and characterisation of a 3D multi-cellular in vitro model of normal human breast: a tool for cancer initiation studies
Multicellular 3-dimensional (3D) in vitro models of normal human breast tissue to study cancer initiation are required. We present a model incorporating three of the major functional cell types of breast, detail the phenotype and document our breast cancer initiation studies. Myoepithelial cells and...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Impact Journals LLC
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4537045/ https://www.ncbi.nlm.nih.gov/pubmed/25915532 |
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author | Nash, Claire E. Mavria, Georgia Baxter, Euan W. Holliday, Deborah L. Tomlinson, Darren C. Treanor, Darren Novitskaya, Vera Berditchevski, Fedor Hanby, Andrew M. Speirs, Valerie |
author_facet | Nash, Claire E. Mavria, Georgia Baxter, Euan W. Holliday, Deborah L. Tomlinson, Darren C. Treanor, Darren Novitskaya, Vera Berditchevski, Fedor Hanby, Andrew M. Speirs, Valerie |
author_sort | Nash, Claire E. |
collection | PubMed |
description | Multicellular 3-dimensional (3D) in vitro models of normal human breast tissue to study cancer initiation are required. We present a model incorporating three of the major functional cell types of breast, detail the phenotype and document our breast cancer initiation studies. Myoepithelial cells and fibroblasts were isolated and immortalised from breast reduction mammoplasty samples. Tri-cultures containing non-tumorigenic luminal epithelial cells HB2, or HB2 overexpressing different HER proteins, together with myoepithelial cells and fibroblasts were established in collagen I. Phenotype was assessed morphologically and immunohistochemically and compared to normal breast tissue. When all three cell types were present, polarised epithelial structures with lumens and basement membrane production were observed, akin to normal human breast tissue. Overexpression of HER2 or HER2/3 caused a significant increase in size, while HER2 overexpression resulted in development of a DCIS-like phenotype. In summary, we have developed a 3D tri-cellular model of normal human breast, amenable to comparative analysis after genetic manipulation and with potential to dissect the mechanisms behind the early stages of breast cancer initiation. |
format | Online Article Text |
id | pubmed-4537045 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Impact Journals LLC |
record_format | MEDLINE/PubMed |
spelling | pubmed-45370452015-08-26 Development and characterisation of a 3D multi-cellular in vitro model of normal human breast: a tool for cancer initiation studies Nash, Claire E. Mavria, Georgia Baxter, Euan W. Holliday, Deborah L. Tomlinson, Darren C. Treanor, Darren Novitskaya, Vera Berditchevski, Fedor Hanby, Andrew M. Speirs, Valerie Oncotarget Research Paper Multicellular 3-dimensional (3D) in vitro models of normal human breast tissue to study cancer initiation are required. We present a model incorporating three of the major functional cell types of breast, detail the phenotype and document our breast cancer initiation studies. Myoepithelial cells and fibroblasts were isolated and immortalised from breast reduction mammoplasty samples. Tri-cultures containing non-tumorigenic luminal epithelial cells HB2, or HB2 overexpressing different HER proteins, together with myoepithelial cells and fibroblasts were established in collagen I. Phenotype was assessed morphologically and immunohistochemically and compared to normal breast tissue. When all three cell types were present, polarised epithelial structures with lumens and basement membrane production were observed, akin to normal human breast tissue. Overexpression of HER2 or HER2/3 caused a significant increase in size, while HER2 overexpression resulted in development of a DCIS-like phenotype. In summary, we have developed a 3D tri-cellular model of normal human breast, amenable to comparative analysis after genetic manipulation and with potential to dissect the mechanisms behind the early stages of breast cancer initiation. Impact Journals LLC 2015-04-12 /pmc/articles/PMC4537045/ /pubmed/25915532 Text en Copyright: © 2015 Nash et al. http://creativecommons.org/licenses/by/2.5/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Paper Nash, Claire E. Mavria, Georgia Baxter, Euan W. Holliday, Deborah L. Tomlinson, Darren C. Treanor, Darren Novitskaya, Vera Berditchevski, Fedor Hanby, Andrew M. Speirs, Valerie Development and characterisation of a 3D multi-cellular in vitro model of normal human breast: a tool for cancer initiation studies |
title | Development and characterisation of a 3D multi-cellular in vitro model of normal human breast: a tool for cancer initiation studies |
title_full | Development and characterisation of a 3D multi-cellular in vitro model of normal human breast: a tool for cancer initiation studies |
title_fullStr | Development and characterisation of a 3D multi-cellular in vitro model of normal human breast: a tool for cancer initiation studies |
title_full_unstemmed | Development and characterisation of a 3D multi-cellular in vitro model of normal human breast: a tool for cancer initiation studies |
title_short | Development and characterisation of a 3D multi-cellular in vitro model of normal human breast: a tool for cancer initiation studies |
title_sort | development and characterisation of a 3d multi-cellular in vitro model of normal human breast: a tool for cancer initiation studies |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4537045/ https://www.ncbi.nlm.nih.gov/pubmed/25915532 |
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