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Redirecting Normal and Cancer Stem Cells to a Mammary Epithelial Cell Fate
Anastasia Frank-Kamenetskii1, Brian W Booth2
1Department of Bioengineering, Clemson University, 401-1 Rhodes Engineering Research Center, Clemson, SC, 29634, USA.
Normal mouse mammary stem cell niches can guide non-mammary cells, including tumor cells, to differentiate into mammary epithelial cells. These cells lose their cancer-forming potential within the supportive tissue microenvironment.
Area of Science:
- Stem cell biology
- Developmental biology
- Cancer research
Background:
- Tissue microenvironments, or stem cell niches, regulate resident and surrounding cells.
- These niches control tissue homeostasis, including proliferation, differentiation, healing, remodeling, and tumorigenesis.
- Intercellular signals from stem and non-stem cells are crucial for these processes.
Purpose of the Study:
- To review recent discoveries on the influence of normal mouse mammary microenvironments on cell fate.
- To explore the capacity of mammary stem cell niches to guide non-mammary cells.
- To summarize how mammary niches affect tumor-derived cells.
Main Methods:
- Review of recent publications on mouse mammary stem cell niches.
- Analysis of studies involving the introduction of non-mammary and tumor-derived cells into mammary niches.
- Examination of gene expression profiles and differentiation patterns.
Main Results:
- Normal mouse mammary microenvironments guide differentiation of non-mammary cells, including tumor cells.
- Non-mammary cells introduced into mammary stem cell niches proliferate and differentiate into mammary epithelial lineages.
- Tumor-derived cells adopt mammary epithelial phenotypes, lose cancer-forming capacity, and shift gene expression towards normal profiles.
Conclusions:
- The normal mouse mammary microenvironment possesses a remarkable ability to dictate cell fate.
- Mammary stem cell niches can reprogram non-mammary and malignant cells towards a normal epithelial phenotype.
- This reprogramming highlights the plasticity of cell identity influenced by the stem cell niche.
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