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

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Katharina Theresa Kohler
Nadine Goldhammer
Samuel Demharter
Ulrich Pfisterer
Konstantin Khodosevich
Lone Rønnov-Jessen
Ole William Petersen
René Villadsen
Jiyoung Kim
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[1] University of Copenhagen,Department of Cellular and Molecular Medicine, Faculty of Health and Medical Sciences
[2] University of Copenhagen,Novo Nordisk Foundation Center for Stem Cell Biology, Faculty of Health and Medical Sciences
[3] University of Copenhagen,Biotech Research and Innovation Center, Faculty of Health and Medical Sciences
[4] University of Copenhagen,Section for Cell Biology and Physiology, Department of Biology, Faculty of Science
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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.
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