Cellular Plasticity of Mammary Epithelial Cells Underlies Heterogeneity of Breast Cancer.

Biomedicines

Institut Curie, PSL Research University, INSERM U934, CNRS UMR3215, F-75248 Paris CEDEX 05, France.

Published: November 2018

AI Article Synopsis

  • The relationships between stem cells, progenitor cells, and differentiated cells in various tissues, including the mouse mammary gland, are complex due to cell plasticity allowing state switching.
  • Unipotent progenitors in the mammary gland maintain the epithelial tissue but can revert to multipotent states during regeneration or oncogene activation.
  • The review explores how these cellular dynamics relate to tumor development and highlights the impact of specific genetic mutations on tumor types, which is essential for tailoring breast cancer treatments.

Article Abstract

The hierarchical relationships between stem cells, lineage-committed progenitors, and differentiated cells remain unclear in several tissues, due to a high degree of cell plasticity, allowing cells to switch between different cell states. The mouse mammary gland, similarly to other tissues such as the prostate, the sweat gland, and the respiratory tract airways, consists of an epithelium exclusively maintained by unipotent progenitors throughout adulthood. Such unipotent progenitors, however, retain a remarkable cellular plasticity, as they can revert to multipotency during epithelial regeneration as well as upon oncogene activation. Here, we revise the current knowledge on mammary cell hierarchies in light of the most recent lineage tracing studies performed in the mammary gland and highlight how stem cell differentiation or reversion to multipotency are at the base of tumor development and progression. In addition, we will discuss the current knowledge about the interplay between tumor cells of origin and defined genetic mutations, leading to different tumor types, and its implications in choosing specific therapeutic protocols for breast cancer patients.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6315661PMC
http://dx.doi.org/10.3390/biomedicines6040103DOI Listing

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