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Phenotypic plasticity in normal breast derived epithelial cells

BACKGROUND: Normal, healthy human breast tissue from a variety of volunteer donors has become available for research thanks to the establishment of the Susan G. Komen for the Cure® Tissue Bank at the IU Simon Cancer Center (KTB). Multiple epithelial (K-HME) and stromal cells (K-HMS) were established...

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Autores principales: Sauder, Candice AM, Koziel, Jillian E, Choi, MiRan, Fox, Melanie J, Grimes, Brenda R, Badve, Sunil, Blosser, Rachel J, Radovich, Milan, Lam, Christina C, Vaughan, Melville B, Herbert, Brittney-Shea, Clare, Susan E
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4066279/
https://www.ncbi.nlm.nih.gov/pubmed/24915897
http://dx.doi.org/10.1186/1471-2121-15-20
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author Sauder, Candice AM
Koziel, Jillian E
Choi, MiRan
Fox, Melanie J
Grimes, Brenda R
Badve, Sunil
Blosser, Rachel J
Radovich, Milan
Lam, Christina C
Vaughan, Melville B
Herbert, Brittney-Shea
Clare, Susan E
author_facet Sauder, Candice AM
Koziel, Jillian E
Choi, MiRan
Fox, Melanie J
Grimes, Brenda R
Badve, Sunil
Blosser, Rachel J
Radovich, Milan
Lam, Christina C
Vaughan, Melville B
Herbert, Brittney-Shea
Clare, Susan E
author_sort Sauder, Candice AM
collection PubMed
description BACKGROUND: Normal, healthy human breast tissue from a variety of volunteer donors has become available for research thanks to the establishment of the Susan G. Komen for the Cure® Tissue Bank at the IU Simon Cancer Center (KTB). Multiple epithelial (K-HME) and stromal cells (K-HMS) were established from the donated tissue. Explant culture was utilized to isolate the cells from pieces of breast tissue. Selective media and trypsinization were employed to select either epithelial cells or stromal cells. The primary, non-transformed epithelial cells, the focus of this study, were characterized by immunohistochemistry, flow cytometry, and in vitro cell culture. RESULTS: All of the primary, non-transformed epithelial cells tested have the ability to differentiate in vitro into a variety of cell types when plated in or on biologic matrices. Cells identified include stratified squamous epithelial, osteoclasts, chondrocytes, adipocytes, neural progenitors/neurons, immature muscle and melanocytes. The cells also express markers of embryonic stem cells. CONCLUSIONS: The cell culture conditions employed select an epithelial cell that is pluri/multipotent. The plasticity of the epithelial cells developed mimics that seen in metaplastic carcinoma of the breast (MCB), a subtype of triple negative breast cancer; and may provide clues to the origin of this particularly aggressive type of breast cancer. The KTB is a unique biorepository, and the normal breast epithelial cells isolated from donated tissue have significant potential as new research tools.
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spelling pubmed-40662792014-06-24 Phenotypic plasticity in normal breast derived epithelial cells Sauder, Candice AM Koziel, Jillian E Choi, MiRan Fox, Melanie J Grimes, Brenda R Badve, Sunil Blosser, Rachel J Radovich, Milan Lam, Christina C Vaughan, Melville B Herbert, Brittney-Shea Clare, Susan E BMC Cell Biol Research Article BACKGROUND: Normal, healthy human breast tissue from a variety of volunteer donors has become available for research thanks to the establishment of the Susan G. Komen for the Cure® Tissue Bank at the IU Simon Cancer Center (KTB). Multiple epithelial (K-HME) and stromal cells (K-HMS) were established from the donated tissue. Explant culture was utilized to isolate the cells from pieces of breast tissue. Selective media and trypsinization were employed to select either epithelial cells or stromal cells. The primary, non-transformed epithelial cells, the focus of this study, were characterized by immunohistochemistry, flow cytometry, and in vitro cell culture. RESULTS: All of the primary, non-transformed epithelial cells tested have the ability to differentiate in vitro into a variety of cell types when plated in or on biologic matrices. Cells identified include stratified squamous epithelial, osteoclasts, chondrocytes, adipocytes, neural progenitors/neurons, immature muscle and melanocytes. The cells also express markers of embryonic stem cells. CONCLUSIONS: The cell culture conditions employed select an epithelial cell that is pluri/multipotent. The plasticity of the epithelial cells developed mimics that seen in metaplastic carcinoma of the breast (MCB), a subtype of triple negative breast cancer; and may provide clues to the origin of this particularly aggressive type of breast cancer. The KTB is a unique biorepository, and the normal breast epithelial cells isolated from donated tissue have significant potential as new research tools. BioMed Central 2014-06-10 /pmc/articles/PMC4066279/ /pubmed/24915897 http://dx.doi.org/10.1186/1471-2121-15-20 Text en Copyright © 2014 Sauder et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited.
spellingShingle Research Article
Sauder, Candice AM
Koziel, Jillian E
Choi, MiRan
Fox, Melanie J
Grimes, Brenda R
Badve, Sunil
Blosser, Rachel J
Radovich, Milan
Lam, Christina C
Vaughan, Melville B
Herbert, Brittney-Shea
Clare, Susan E
Phenotypic plasticity in normal breast derived epithelial cells
title Phenotypic plasticity in normal breast derived epithelial cells
title_full Phenotypic plasticity in normal breast derived epithelial cells
title_fullStr Phenotypic plasticity in normal breast derived epithelial cells
title_full_unstemmed Phenotypic plasticity in normal breast derived epithelial cells
title_short Phenotypic plasticity in normal breast derived epithelial cells
title_sort phenotypic plasticity in normal breast derived epithelial cells
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4066279/
https://www.ncbi.nlm.nih.gov/pubmed/24915897
http://dx.doi.org/10.1186/1471-2121-15-20
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