Cargando…

Ductal keratin 15(+) luminal progenitors in normal breast exhibit a basal-like breast cancer transcriptomic signature

Normal breast luminal epithelial progenitors have been implicated as cell of origin in basal-like breast cancer, but their anatomical localization remains understudied. Here, we combine collection under the microscope of organoids from reduction mammoplasties and single-cell mRNA sequencing (scRNA-s...

Descripción completa

Detalles Bibliográficos
Autores principales: Kohler, Katharina Theresa, Goldhammer, Nadine, Demharter, Samuel, Pfisterer, Ulrich, Khodosevich, Konstantin, Rønnov-Jessen, Lone, Petersen, Ole William, Villadsen, René, Kim, Jiyoung
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9276673/
https://www.ncbi.nlm.nih.gov/pubmed/35821504
http://dx.doi.org/10.1038/s41523-022-00444-8
_version_ 1784745778658410496
author Kohler, Katharina Theresa
Goldhammer, Nadine
Demharter, Samuel
Pfisterer, Ulrich
Khodosevich, Konstantin
Rønnov-Jessen, Lone
Petersen, Ole William
Villadsen, René
Kim, Jiyoung
author_facet Kohler, Katharina Theresa
Goldhammer, Nadine
Demharter, Samuel
Pfisterer, Ulrich
Khodosevich, Konstantin
Rønnov-Jessen, Lone
Petersen, Ole William
Villadsen, René
Kim, Jiyoung
author_sort Kohler, Katharina Theresa
collection PubMed
description Normal breast luminal epithelial progenitors have been implicated as cell of origin in basal-like breast cancer, but their anatomical localization remains understudied. Here, we combine collection under the microscope of organoids from reduction mammoplasties and single-cell mRNA sequencing (scRNA-seq) of FACS-sorted luminal epithelial cells with multicolor imaging to profile ducts and terminal duct lobular units (TDLUs) and compare them with breast cancer subtypes. Unsupervised clustering reveals eleven distinct clusters and a differentiation trajectory starting with keratin 15(+) (K15(+)) progenitors enriched in ducts. Spatial mapping of luminal progenitors is confirmed at the protein level by staining with critical duct markers. Comparison of the gene expression profiles of normal luminal cells with those of breast cancer subtypes suggests a strong correlation between normal breast ductal progenitors and basal-like breast cancer. We propose that K15(+) basal-like breast cancers originate in ductal progenitors, which emphasizes the importance of not only lineages but also cellular position within the ductal-lobular tree.
format Online
Article
Text
id pubmed-9276673
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher Nature Publishing Group UK
record_format MEDLINE/PubMed
spelling pubmed-92766732022-07-14 Ductal keratin 15(+) luminal progenitors in normal breast exhibit a basal-like breast cancer transcriptomic signature Kohler, Katharina Theresa Goldhammer, Nadine Demharter, Samuel Pfisterer, Ulrich Khodosevich, Konstantin Rønnov-Jessen, Lone Petersen, Ole William Villadsen, René Kim, Jiyoung NPJ Breast Cancer Article Normal breast luminal epithelial progenitors have been implicated as cell of origin in basal-like breast cancer, but their anatomical localization remains understudied. Here, we combine collection under the microscope of organoids from reduction mammoplasties and single-cell mRNA sequencing (scRNA-seq) of FACS-sorted luminal epithelial cells with multicolor imaging to profile ducts and terminal duct lobular units (TDLUs) and compare them with breast cancer subtypes. Unsupervised clustering reveals eleven distinct clusters and a differentiation trajectory starting with keratin 15(+) (K15(+)) progenitors enriched in ducts. Spatial mapping of luminal progenitors is confirmed at the protein level by staining with critical duct markers. Comparison of the gene expression profiles of normal luminal cells with those of breast cancer subtypes suggests a strong correlation between normal breast ductal progenitors and basal-like breast cancer. We propose that K15(+) basal-like breast cancers originate in ductal progenitors, which emphasizes the importance of not only lineages but also cellular position within the ductal-lobular tree. Nature Publishing Group UK 2022-07-12 /pmc/articles/PMC9276673/ /pubmed/35821504 http://dx.doi.org/10.1038/s41523-022-00444-8 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/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/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Kohler, Katharina Theresa
Goldhammer, Nadine
Demharter, Samuel
Pfisterer, Ulrich
Khodosevich, Konstantin
Rønnov-Jessen, Lone
Petersen, Ole William
Villadsen, René
Kim, Jiyoung
Ductal keratin 15(+) luminal progenitors in normal breast exhibit a basal-like breast cancer transcriptomic signature
title Ductal keratin 15(+) luminal progenitors in normal breast exhibit a basal-like breast cancer transcriptomic signature
title_full Ductal keratin 15(+) luminal progenitors in normal breast exhibit a basal-like breast cancer transcriptomic signature
title_fullStr Ductal keratin 15(+) luminal progenitors in normal breast exhibit a basal-like breast cancer transcriptomic signature
title_full_unstemmed Ductal keratin 15(+) luminal progenitors in normal breast exhibit a basal-like breast cancer transcriptomic signature
title_short Ductal keratin 15(+) luminal progenitors in normal breast exhibit a basal-like breast cancer transcriptomic signature
title_sort ductal keratin 15(+) luminal progenitors in normal breast exhibit a basal-like breast cancer transcriptomic signature
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9276673/
https://www.ncbi.nlm.nih.gov/pubmed/35821504
http://dx.doi.org/10.1038/s41523-022-00444-8
work_keys_str_mv AT kohlerkatharinatheresa ductalkeratin15luminalprogenitorsinnormalbreastexhibitabasallikebreastcancertranscriptomicsignature
AT goldhammernadine ductalkeratin15luminalprogenitorsinnormalbreastexhibitabasallikebreastcancertranscriptomicsignature
AT demhartersamuel ductalkeratin15luminalprogenitorsinnormalbreastexhibitabasallikebreastcancertranscriptomicsignature
AT pfistererulrich ductalkeratin15luminalprogenitorsinnormalbreastexhibitabasallikebreastcancertranscriptomicsignature
AT khodosevichkonstantin ductalkeratin15luminalprogenitorsinnormalbreastexhibitabasallikebreastcancertranscriptomicsignature
AT rønnovjessenlone ductalkeratin15luminalprogenitorsinnormalbreastexhibitabasallikebreastcancertranscriptomicsignature
AT petersenolewilliam ductalkeratin15luminalprogenitorsinnormalbreastexhibitabasallikebreastcancertranscriptomicsignature
AT villadsenrene ductalkeratin15luminalprogenitorsinnormalbreastexhibitabasallikebreastcancertranscriptomicsignature
AT kimjiyoung ductalkeratin15luminalprogenitorsinnormalbreastexhibitabasallikebreastcancertranscriptomicsignature