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Biological and Molecular Heterogeneity of Breast Cancers Correlates with Their Cancer Stem Cell Content
Author(s) -
Salvatore Pece,
Daniela Tosoni,
Stefano Confalonieri,
Giovanni Mazzarol,
Manuela Vecchi,
Simona Ronzoni,
Loris Bernard,
Giuseppe Viale,
Pier Giuseppe Pelicci,
Pier Paolo Di Fiore
Publication year - 2010
Publication title -
cell
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 26.304
H-Index - 776
eISSN - 1097-4172
pISSN - 0092-8674
DOI - 10.1016/j.cell.2009.12.007
Subject(s) - biology , breast cancer , cancer research , cancer stem cell , xenotransplantation , phenotype , cancer , stem cell , cell , mammary gland , gene , transplantation , medicine , microbiology and biotechnology , genetics
Pathways that govern stem cell (SC) function are often subverted in cancer. Here, we report the isolation to near purity of human normal mammary SCs (hNMSCs), from cultured mammospheres, on the basis of their ability to retain the lipophilic dye PKH26 as a consequence of their quiescent nature. PKH26-positive cells possess all the characteristics of hNMSCs. The transcriptional profile of PKH26-positive cells (hNMSC signature) was able to predict biological and molecular features of breast cancers. By using markers of the hNMSC signature, we prospectively isolated SCs from the normal gland and from breast tumors. Poorly differentiated (G3) cancers displayed higher content of prospectively isolated cancer SCs (CSCs) than did well-differentiated (G1) cancers. By comparing G3 and G1 tumors in xenotransplantation experiments, we directly demonstrated that G3s are enriched in CSCs. Our data support the notion that the heterogeneous phenotypical and molecular traits of human breast cancers are a function of their CSC content.

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