Immune-induced epithelial to mesenchymal transition in vivo generates breast cancer stem cells
Palabras clave : 
Mammary neoplasms
Epithelial cells
Antigens, CD24
Antigens, CD44
Fecha de publicación: 
1-abr-2009
Editorial : 
American Association for Cancer Research
ISSN: 
0008-5472
Cita: 
Santisteban M, Reiman JM, Asiedu MK, Behrens MD, Nassar A, Kalli KR, et al. Immune-induced epithelial to mesenchymal transition in vivo generates breast cancer stem cells. Cancer Res. 2009 Apr 1;69(7):2887-2895
Resumen
The breast cancer stem cell (BCSC) hypotheses suggest that breast cancer is derived from a single tumor-initiating cell with stem-like properties, but the source of these cells is unclear. We previously observed that induction of an immune response against an epithelial breast cancer led in vivo to the T-cell-dependent outgrowth of a tumor, the cells of which had undergone epithelial to mesenchymal transition (EMT). The resulting mesenchymal tumor cells had a CD24(-/lo)CD44(+) phenotype, consistent with BCSCs. In the present study, we found that EMT was induced by CD8 T cells and the resulting tumors had characteristics of BCSCs, including potent tumorigenicity, ability to reestablish an epithelial tumor, and enhanced resistance to drugs and radiation. In contrast to the hierarchal cancer stem cell hypothesis, which suggests that breast cancer arises from the transformation of a resident tissue stem cell, our results show that EMT can produce the BCSC phenotype. These findings have several important implications related to disease progression and relapse.

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Fichero: 
nihms92056.pdf
Descripción: 
Tamaño: 
2,71 MB
Formato: 
Adobe PDF


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