Molecular definition of breast tumor heterogeneity

被引:1169
作者
Shipitsin, Michail
Campbell, Lauren L.
Argani, Pedram
Werernowicz, Stanislawa
Bloushtain-Qimron, Noga
Yao, Jun
Nikolskaya, Tatiana
Serebryiskaya, Tatiana
Beroukhim, Rameen
Hu, Min
Halushka, Marc K.
Sukumar, Saraswati
Parker, Leroy M.
Anderson, Karen S.
Harris, Lyndsay N.
Garber, Judy E.
Richardson, Andrea L.
Schnitt, Stuart J.
Nikolsky, Yuri
Gelman, Rebecca S.
Polyak, Kornelia [1 ]
机构
[1] Dana Farber Canc Inst, Dept Med Oncol, Boston, MA 02115 USA
[2] Dana Farber Canc Inst, Dept Biostat & Computat Biol, Boston, MA 02115 USA
[3] Harvard Univ, Dept Med, Boston, MA 02115 USA
[4] Harvard Univ, Dept Pathol, Boston, MA 02115 USA
[5] Harvard Univ, Program Biol & Biomed Sci, Boston, MA 02115 USA
[6] Johns Hopkins Univ, Sch Med, Baltimore, MD 21231 USA
[7] GeneGo Inc, St Joseph, MI 49085 USA
[8] NI Vavilov Gen Genet Res Inst, Moscow 117809, Russia
[9] Harvard Univ, Sch Publ Hlth, Dept Biostat, Boston, MA 02115 USA
[10] Brigham & Womens Hosp, Dept Pathol, Boston, MA 02115 USA
[11] Beth Israel Deaconess Med Ctr, Dept Pathol, Boston, MA 02115 USA
关键词
D O I
10.1016/j.ccr.2007.01.013
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Cells with distinct phenotypes including stem-cell-like properties have been proposed to exist in normal human mammary epithelium and breast carcinomas, but their detailed molecular characteristics and clinical significance are unclear. We determined gene expression and genetic profiles of cells purified from cancerous and normal breast tissue using markers previously associated with stem-cell-like properties. CD24+ and CD44+ cells from individual tumors were clonally related but not always identical. CD44+ cell-specific genes included many known stem-cell markers and correlated with decreased patient survival. The TGF-beta pathway was specifically active in CD44+ cancer cells, where its inhibition induced a more epithelial phenotype. Our data suggest prognostic relevance of CD44+ cells and therapeutic targeting of distinct tumor cell populations.
引用
收藏
页码:259 / 273
页数:15
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