Biological and Molecular Heterogeneity of Breast Cancers Correlates with Their Cancer Stem Cell Content

被引:757
作者
Pece, Salvatore [1 ,2 ,3 ]
Tosoni, Daniela [1 ,3 ]
Confalonieri, Stefano [1 ]
Mazzarol, Giovanni [3 ]
Vecchi, Manuela [1 ]
Ronzoni, Simona [3 ]
Bernard, Loris [3 ]
Viale, Giuseppe [2 ,3 ]
Pelicci, Pier Giuseppe [2 ,3 ]
Di Fiore, Pier Paolo [1 ,2 ,3 ]
机构
[1] Fdn Ist FIRC Oncol Mol, IFOM, I-20139 Milan, Italy
[2] Univ Milan, Dipartimento Med Chirurg & Odontoiatria, I-20122 Milan, Italy
[3] Ist Europeo Oncol, I-20141 Milan, Italy
关键词
MAMMARY-GLAND; IN-VIVO; DIFFERENTIATION; POPULATION; TUMORS; RECONSTRUCTION; MORPHOGENESIS; PROGENITORS; CARCINOMAS; DIVISIONS;
D O I
10.1016/j.cell.2009.12.007
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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.
引用
收藏
页码:62 / 73
页数:12
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