The p53 Pathway Encounters the MicroRNA World

被引:27
作者
Takwi, Apana
Li, Yong [1 ]
机构
[1] Univ Louisville, Sch Med, Dept Biochem & Mol Biol, Louisville, KY 40202 USA
关键词
MicroRNA; p53; TUMOR-SUPPRESSOR; CANCER; EXPRESSION; MIR-34A; TARGETS; MODULATION; MECHANISMS; APOPTOSIS; LATS2;
D O I
10.2174/138920209788185270
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
The p53 protein is a transcription factor that regulates multiple cellular processes in human and other high eukaryotes including cell proliferation, differentiation, cell cycle, and metabolism. The central roles played by p53 in tumor development have drawn extensive studies on p53 activation and inactivation. The regulation of p53 and its pathway, as well as its transactivational targets is of prime importance in the understanding of tumorigenesis. Recently, microRNAs (miRNAs) have been reported to be directly transactivated by p53. Equally, p53 and components of its pathway have been shown to be targeted by miRNA thereby affecting p53 activities. In this review, we focus our discussion on the biological and pathological roles of miRNAs in the p53 pathway.
引用
收藏
页码:194 / 197
页数:4
相关论文
共 36 条
[1]   p53-mediated activation of miRNA34 candidate tumor-suppressor genes [J].
Bommer, Guido T. ;
Gerin, Isabelle ;
Feng, Ying ;
Kaczorowski, Andrew J. ;
Kuick, Rork ;
Love, Robert E. ;
Zhai, Yali ;
Giordano, Thomas J. ;
Qin, Zhaohui S. ;
Moore, Bethany B. ;
MacDougald, Ormond A. ;
Cho, Kathleen R. ;
Fearon, Eric R. .
CURRENT BIOLOGY, 2007, 17 (15) :1298-1307
[2]   p53-Responsive MicroRNAs 192 and 215 Are Capable of Inducing Cell Cycle Arrest [J].
Braun, Christian J. ;
Zhang, Xin ;
Savelyeva, Irina ;
Wolff, Sonja ;
Moll, Ute M. ;
Schepeler, Troels ;
Orntoft, Torben F. ;
Andersen, Claus L. ;
Dobbelstein, Matthias .
CANCER RESEARCH, 2008, 68 (24) :10094-10104
[3]   Developmental defects and p53 hyperacetylation in Sir2 homolog (SIRT1)-deficient mice [J].
Cheng, HL ;
Mostoslavsky, R ;
Saito, S ;
Manis, JP ;
Gu, YS ;
Patel, P ;
Bronson, R ;
Appella, E ;
Alt, FW ;
Chua, KF .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2003, 100 (19) :10794-10799
[4]   Implications of micro-RNA profiling for cancer diagnosis [J].
Cummins, J. M. ;
Velculescu, V. E. .
ONCOGENE, 2006, 25 (46) :6220-6227
[5]   Mechanisms of translational control by the 3′ UTR in development and differentiation [J].
de Moor, CH ;
Meijer, H ;
Lissenden, S .
SEMINARS IN CELL & DEVELOPMENTAL BIOLOGY, 2005, 16 (01) :49-58
[6]   Rho GTPases: functions and association with cancer [J].
Ellenbroek, Saskia I. J. ;
Collard, John G. .
CLINICAL & EXPERIMENTAL METASTASIS, 2007, 24 (08) :657-672
[7]  
Fei PW, 2002, CANCER RES, V62, P7316
[8]   MicroRNA expression and function in cancer [J].
Garzon, Ramiro ;
Fabbri, Muller ;
Cimmino, Amelia ;
Calin, George A. ;
Croce, Carlo M. .
TRENDS IN MOLECULAR MEDICINE, 2006, 12 (12) :580-587
[9]   Coordinated Regulation of Cell Cycle Transcripts by p53-inducible microRNAs, miR-192 and miR-215 [J].
Georges, Sara A. ;
Biery, Matthew C. ;
Kim, Soo-yeon ;
Schelter, Janell M. ;
Guo, Jane ;
Chang, Aaron N. ;
Jackson, Aimee L. ;
Carleton, Michael O. ;
Linsley, Peter S. ;
Cleary, Michele A. ;
Chau, B. Nelson .
CANCER RESEARCH, 2008, 68 (24) :10105-10112
[10]   A microRNA component of the p53 tumour suppressor network [J].
He, Lin ;
He, Xingyue ;
Lim, Lee P. ;
De Stanchina, Elisa ;
Xuan, Zhenyu ;
Liang, Yu ;
Xue, Wen ;
Zender, Lars ;
Magnus, Jill ;
Ridzon, Dana ;
Jackson, Aimee L. ;
Linsley, Peter S. ;
Chen, Caifu ;
Lowe, Scott W. ;
Cleary, Michele A. ;
Hannon, Gregory J. .
NATURE, 2007, 447 (7148) :1130-U16