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Organoid cultures from normal and cancer-prone human breast tissues preserve complex epithelial lineages.
- Source :
-
Nature communications [Nat Commun] 2020 Apr 06; Vol. 11 (1), pp. 1711. Date of Electronic Publication: 2020 Apr 06. - Publication Year :
- 2020
-
Abstract
- 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.
- Subjects :
- Adult
BRCA1 Protein genetics
Breast Neoplasms
Cell Differentiation genetics
Cell Differentiation physiology
Epidermal Growth Factor pharmacology
ErbB Receptors metabolism
Female
Humans
Mammary Glands, Human chemistry
Mammary Glands, Human metabolism
Middle Aged
Organoids chemistry
Single-Cell Analysis
Stem Cells chemistry
Stem Cells metabolism
Transforming Growth Factor beta antagonists & inhibitors
Young Adult
p38 Mitogen-Activated Protein Kinases antagonists & inhibitors
Cell Culture Techniques methods
Cell Lineage genetics
Mammary Glands, Human cytology
Organoids cytology
Organoids metabolism
Stem Cells cytology
Subjects
Details
- Language :
- English
- ISSN :
- 2041-1723
- Volume :
- 11
- Issue :
- 1
- Database :
- MEDLINE
- Journal :
- Nature communications
- Publication Type :
- Academic Journal
- Accession number :
- 32249764
- Full Text :
- https://doi.org/10.1038/s41467-020-15548-7