Myc-Induced MicroRNAs Integrate Myc-Mediated Cell Proliferation and Cell Fate

被引:44
作者
Kim, Jong Wook [1 ,2 ]
Mori, Seiichi [3 ]
Nevins, Joseph R. [1 ,2 ]
机构
[1] Duke Univ, Med Ctr, Duke Inst Genome Sci & Policy, Durham, NC 27710 USA
[2] Duke Univ, Med Ctr, Dept Mol Genet & Microbiol, Durham, NC 27710 USA
[3] Natl Univ Singapore, Canc Sci Inst Singapore, Genom Oncol Programme, Singapore 117548, Singapore
关键词
C-MYC; TRANSCRIPTIONAL REPRESSION; EXPRESSION; GROWTH; CYCLE; RECRUITMENT; SUPPRESSION; TRANSFORMATION; P21(CIP1); MIR-222;
D O I
10.1158/0008-5472.CAN-10-0659
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The Myc pathway, often deregulated in cancer, is critical in determining cell fate by coordinating a gene expression program that links the control of cell proliferation with cell fate decisions. As such, precise control of the Myc pathway activity must be achieved to ensure faithful execution of appropriate cellular response and to prevent progressing toward a malignant state. With recent highlighted roles of microRNAs ( miRNA) as critical components of gene control, we sought to evaluate the extent to which miRNAs may contribute in the execution of Myc function. Combined analysis of mRNA and miRNA expression profiles reveals an integration whereby the Myc-mediated induction of miRNAs leads to the repression of various mRNAs encoding tumor suppressors that block cell proliferation including p21, p27, and Rb. In addition, the proapoptotic PTEN tumor suppressor gene is also repressed by Myc-induced miRNAs, suggesting that Myc-induced miRNAs contribute to the precise control of a transcriptional program that coordinates the balance of cell proliferation and cell death. Cancer Res; 70( 12); 4820-8. (C)2010 AACR.
引用
收藏
页码:4820 / 4828
页数:9
相关论文
共 47 条
[1]   Transcriptional regulation and transformation by MYC proteins [J].
Adhikary, S ;
Eilers, M .
NATURE REVIEWS MOLECULAR CELL BIOLOGY, 2005, 6 (08) :635-645
[2]   MicroRNAs: Genomics, biogenesis, mechanism, and function (Reprinted from Cell, vol 116, pg 281-297, 2004) [J].
Bartel, David P. .
CELL, 2007, 131 (04) :11-29
[3]   Oncogenic pathway signatures in human cancers as a guide to targeted therapies [J].
Bild, AH ;
Yao, G ;
Chang, JT ;
Wang, QL ;
Potti, A ;
Chasse, D ;
Joshi, MB ;
Harpole, D ;
Lancaster, JM ;
Berchuck, A ;
Olson, JA ;
Marks, JR ;
Dressman, HK ;
West, M ;
Nevins, JR .
NATURE, 2006, 439 (7074) :353-357
[4]   Myc represses transcription through recruitment of DNA methyltransferase corepressor [J].
Brenner, C ;
Deplus, R ;
Didelot, C ;
Loriot, A ;
Viré, E ;
De Smet, C ;
Gutierrez, A ;
Danovi, D ;
Bernard, D ;
Boon, T ;
Pelicci, PG ;
Amati, B ;
Kouzarides, T ;
de Launoit, Y ;
Di Croce, L ;
Fuks, F .
EMBO JOURNAL, 2005, 24 (02) :336-346
[5]   A sensitive array for microRNA expression profiling (miChip) based on locked nucleic acids (LNA) [J].
Castoldi, M ;
Schmidt, S ;
Benes, V ;
Noerholm, M ;
Kulozik, AE ;
Hentze, MW ;
Muckenthaler, MU .
RNA, 2006, 12 (05) :913-920
[6]   Widespread microRNA repression by Myc contributes to tumorigenesis [J].
Chang, Tsung-Cheng ;
Yu, Duonan ;
Lee, Yun-Sil ;
Wentzel, Erik A. ;
Arking, Dan E. ;
West, Kristin M. ;
Dang, Chi V. ;
Thomas-Tikhonenko, Andrei ;
Mendell, Joshua T. .
NATURE GENETICS, 2008, 40 (01) :43-50
[7]   Lin-28B transactivation is necessary for Myc-mediated let-7 repression and proliferation [J].
Chang, Tsung-Cheng ;
Zeiteis, Lauren R. ;
Hwang, Hun-Way ;
Chivukula, Raghu R. ;
Wentzel, Erik A. ;
Dews, Michael ;
Jung, Jason ;
Gao, Ping ;
Dang, Chi V. ;
Beer, Michael A. ;
Thomas-Tikhonenko, Andrei ;
Mendell, Joshua T. .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2009, 106 (09) :3384-3389
[8]   Myc-mediated transformation: the repression connection [J].
Claassen, GF ;
Hann, SR .
ONCOGENE, 1999, 18 (19) :2925-2933
[9]   A role for transcriptional repression of p21CIP1 by c-Myc in overcoming transforming growth factor β-induced cell-cycle arrest [J].
Claassen, GF ;
Hann, SR .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2000, 97 (17) :9498-9503
[10]  
Cole MD, 2006, CURR TOP MICROBIOL, V302, P33