Sequencing of breast cancer stem cell populations indicates a dynamic conversion between differentiation states in vivo
Menée sur des cellules souches cancéreuses et des échantillons de tumeurs primitives prélevés sur 12 patientes atteintes d'un cancer du sein, cette étude de séquençage de l'exome analyse et compare les mutations somatiques observées dans les cellules souches cancéreuses et les cellules tumorales
INTRODUCTION:The cancer stem cell model implies a hierarchical organization within breast tumors maintained by cancer stem-like cells (CSCs). Accordingly, CSCs are a subpopulation of cancer cells with capacity for self-renewal, differentiation and tumor initiation. These cells can be isolated through the phenotypic markers CD44+/CD24-, expression of ALDH1 and an ability to form nonadherent, multicellular spheres in vitro. However, controversies to describe the stem cell model exist; it is unclear whether the tumorigenecity of CSCs in vivo are solely a proxy for a certain genotype. Moreover, in vivo evidence is lacking to fully define the reversibility of CSC differentiation. METHODS:In order to answer these questions, we undertook exome sequencing of CSCs from 12 breast cancer patients, along with paired primary tumor samples. As suggested by stem classical cell biology, we assumed that the number of mutations in the CSC subpopulation should be lower and distinct compared to the differentiated tumor cells with higher proliferation. RESULTS:Our analysis revealed that the majority of somatic mutations are shared between CSCs and bulk primary tumor, with similar frequencies in the two. CONCLUSIONS:The data presented here exclude the possibility that CSCs are only a phenotypic consequence of certain somatic mutations, i.e. a distinct and non-reversible population of cells. In addition, our results imply that CSCs must be a population of cells that can dynamically switch from differentiated tumor cells, and vice versa. This finding increases our understanding of CSC function in tumor heterogeneity and the importance to identify drugs to counter de-differentiation rather than targeting CSCs.