A hybrid epithelial-mesenchymal transition program enables basal epithelial cells to bypass stress-induced stasis and contributes to a metaplastic breast cancer progenitor state

This study reveals how an epigenetic program governs basal epithelial cell fate decisions and contributes to the development of MBC progenitors by restricting access to terminal mesenchymal states that induce growth arrest and, instead, favoring hybrid EMT states with enhanced tumorigenic potential.

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Institutions

Publication Details

Journal
Breast Cancer Research
Published
2024-12-18
DOI
https://doi.org/10.1186/s13058-024-01920-8
Citations
5
Primary Topic
Cancer Cells and Metastasis
Type
article
Field-Weighted Citation Impact
1.41

Funders

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article

A hybrid epithelial-mesenchymal transition program enables basal epithelial cells to bypass stress-induced stasis and contributes to a metaplastic breast cancer progenitor state

Joseph A. Caruso, Chira Chen‐Tanyolac, Thea D. Tlsty
5 citations
Breast Cancer Research
Cancer Cells and Metastasis
1.41
article

A hybrid epithelial-mesenchymal transition program enables basal epithelial cells to bypass stress-induced stasis and contributes to a metaplastic breast cancer progenitor state

Joseph A. Caruso, Chira Chen‐Tanyolac, Thea D. Tlsty
article en
5 citations

Abstract

This study reveals how an epigenetic program governs basal epithelial cell fate decisions and contributes to the development of MBC progenitors by restricting access to terminal mesenchymal states that induce growth arrest and, instead, favoring hybrid EMT states with enhanced tumorigenic potential.

Breast Cancer ResearchVol. 26(1)
University of California, San Francisco (US)
California Breast Cancer Research Program, Cancer Research UK, National Institutes of Health, University of California, San Francisco, National Cancer Institute
Good health and well-being
Openalex Percentile: Top 15%
Cancer Cells and Metastasis
1.41
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