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Organoid cultures from normal and cancer-prone human breast tissues preserve complex epithelial lineages

Recently, organoid technology has been used to generate a large repository of breast cancer organoids. Here we present an extensive evaluation of the ability of organoid culture technology to preserve complex stem/progenitor and differentiated cell types via long-term propagation of normal human mam...

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Autores principales: Rosenbluth, Jennifer M., Schackmann, Ron C. J., Gray, G. Kenneth, Selfors, Laura M., Li, Carman Man-Chung, Boedicker, Mackenzie, Kuiken, Hendrik J., Richardson, Andrea, Brock, Jane, Garber, Judy, Dillon, Deborah, Sachs, Norman, Clevers, Hans, Brugge, Joan S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7136203/
https://www.ncbi.nlm.nih.gov/pubmed/32249764
http://dx.doi.org/10.1038/s41467-020-15548-7
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author Rosenbluth, Jennifer M.
Schackmann, Ron C. J.
Gray, G. Kenneth
Selfors, Laura M.
Li, Carman Man-Chung
Boedicker, Mackenzie
Kuiken, Hendrik J.
Richardson, Andrea
Brock, Jane
Garber, Judy
Dillon, Deborah
Sachs, Norman
Clevers, Hans
Brugge, Joan S.
author_facet Rosenbluth, Jennifer M.
Schackmann, Ron C. J.
Gray, G. Kenneth
Selfors, Laura M.
Li, Carman Man-Chung
Boedicker, Mackenzie
Kuiken, Hendrik J.
Richardson, Andrea
Brock, Jane
Garber, Judy
Dillon, Deborah
Sachs, Norman
Clevers, Hans
Brugge, Joan S.
author_sort Rosenbluth, Jennifer M.
collection PubMed
description Recently, organoid technology has been used to generate a large repository of breast cancer organoids. Here we present an extensive evaluation of the ability of organoid culture technology to preserve complex stem/progenitor and differentiated cell types via long-term propagation of normal human mammary tissues. Basal/stem and luminal progenitor cells can differentiate in culture to generate mature basal and luminal cell types, including ER+ cells that have been challenging to maintain in culture. Cells associated with increased cancer risk can also be propagated. Single-cell analyses of matched organoid cultures and native tissues by mass cytometry for 38 markers provide a higher resolution representation of the multiple mammary epithelial cell types in the organoids, and demonstrate that protein expression patterns of the tissue of origin can be preserved in culture. These studies indicate that organoid cultures provide a valuable platform for studies of mammary differentiation, transformation, and breast cancer risk.
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spelling pubmed-71362032020-04-08 Organoid cultures from normal and cancer-prone human breast tissues preserve complex epithelial lineages Rosenbluth, Jennifer M. Schackmann, Ron C. J. Gray, G. Kenneth Selfors, Laura M. Li, Carman Man-Chung Boedicker, Mackenzie Kuiken, Hendrik J. Richardson, Andrea Brock, Jane Garber, Judy Dillon, Deborah Sachs, Norman Clevers, Hans Brugge, Joan S. Nat Commun Article Recently, organoid technology has been used to generate a large repository of breast cancer organoids. Here we present an extensive evaluation of the ability of organoid culture technology to preserve complex stem/progenitor and differentiated cell types via long-term propagation of normal human mammary tissues. Basal/stem and luminal progenitor cells can differentiate in culture to generate mature basal and luminal cell types, including ER+ cells that have been challenging to maintain in culture. Cells associated with increased cancer risk can also be propagated. Single-cell analyses of matched organoid cultures and native tissues by mass cytometry for 38 markers provide a higher resolution representation of the multiple mammary epithelial cell types in the organoids, and demonstrate that protein expression patterns of the tissue of origin can be preserved in culture. These studies indicate that organoid cultures provide a valuable platform for studies of mammary differentiation, transformation, and breast cancer risk. Nature Publishing Group UK 2020-04-06 /pmc/articles/PMC7136203/ /pubmed/32249764 http://dx.doi.org/10.1038/s41467-020-15548-7 Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Rosenbluth, Jennifer M.
Schackmann, Ron C. J.
Gray, G. Kenneth
Selfors, Laura M.
Li, Carman Man-Chung
Boedicker, Mackenzie
Kuiken, Hendrik J.
Richardson, Andrea
Brock, Jane
Garber, Judy
Dillon, Deborah
Sachs, Norman
Clevers, Hans
Brugge, Joan S.
Organoid cultures from normal and cancer-prone human breast tissues preserve complex epithelial lineages
title Organoid cultures from normal and cancer-prone human breast tissues preserve complex epithelial lineages
title_full Organoid cultures from normal and cancer-prone human breast tissues preserve complex epithelial lineages
title_fullStr Organoid cultures from normal and cancer-prone human breast tissues preserve complex epithelial lineages
title_full_unstemmed Organoid cultures from normal and cancer-prone human breast tissues preserve complex epithelial lineages
title_short Organoid cultures from normal and cancer-prone human breast tissues preserve complex epithelial lineages
title_sort organoid cultures from normal and cancer-prone human breast tissues preserve complex epithelial lineages
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7136203/
https://www.ncbi.nlm.nih.gov/pubmed/32249764
http://dx.doi.org/10.1038/s41467-020-15548-7
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