A Myc Network Accounts for Similarities between Embryonic Stem and Cancer Cell Transcription Programs

被引:592
作者
Kim, Jonghwan [1 ,2 ,3 ,4 ]
Woo, Andrew J. [1 ,2 ,4 ]
Chu, Jianlin [1 ,2 ,3 ,4 ]
Snow, Jonathan W. [1 ,2 ,3 ,4 ]
Fujiwara, Yuko [1 ,2 ,3 ,4 ,5 ]
Kim, Chul Geun [6 ]
Cantor, Alan B. [1 ,2 ,4 ]
Orkin, Stuart H. [1 ,2 ,3 ,4 ,5 ]
机构
[1] Childrens Hosp, Dept Pediat Oncol, Boston, MA 02115 USA
[2] Dana Farber Canc Inst, Boston, MA 02115 USA
[3] Harvard Stem Cell Inst, Boston, MA 02115 USA
[4] Harvard Univ, Sch Med, Boston, MA 02115 USA
[5] Howard Hughes Med Inst, Boston, MA 02115 USA
[6] Hanyang Univ, Dept Life Sci, Seoul 133791, South Korea
关键词
RNAI SCREEN; C-MYC; DEVELOPMENTAL REGULATORS; ESSENTIAL COFACTOR; SELF-RENEWAL; PLURIPOTENCY; COMPLEX; PROTEIN; GENES; TRRAP;
D O I
10.1016/j.cell.2010.09.010
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
c-Myc (Myc) is an important transcriptional regulator in embryonic stem (ES) cells, somatic cell reprogramming, and cancer. Here, we identify a Myc-centered regulatory network in ES cells by combining protein-protein and protein-DNA interaction studies and show that Myc interacts with the NuA4 complex, a regulator of ES cell identity. In combination with regulatory network information, we define three ES cell modules (Core, Polycomb, and Myc) and show that the modules are functionally separable, illustrating that the overall ES cell transcription program is composed of distinct units. With these modules as an analytical tool, we have reassessed the hypothesis linking an ES cell signature with cancer or cancer stem cells. We find that the Myc module, independent of the Core module, is active in various cancers and predicts cancer outcome. The apparent similarity of cancer and ES cell signatures reflects, in large part, the pervasive nature of Myc regulatory networks.
引用
收藏
页码:313 / 324
页数:12
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