MDMX: from bench to bedside

被引:192
作者
Marine, Jean-Christophe W. [1 ]
Dyer, Michael A.
Jochemsen, Aart G.
机构
[1] Univ Ghent VIB, Lab Mol Canc Biol, B-9052 Ghent, Belgium
[2] St Jude Childrens Res Hosp, Dept Dev Neurobiol, Memphis, TN 38105 USA
[3] Leiden Univ, Med Ctr, Dept Mol & Cell Biol, Leiden, Netherlands
关键词
p53; Mdmx; cancer; nutlin;
D O I
10.1242/jcs.03362
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The tumor suppressor protein p53 is negatively regulated by Mdm2, a ubiquitin ligase protein that targets p53 for degradation. Mdmx (also known as Mdm4) is a relative of Mdm2 that was identified on the basis of its ability to physically interact with p53. An increasing body of evidence, including recent genetic studies, suggests that Mdmx also acts as a key negative regulator of p53. Aberrant expression of MDMX could thus contribute to tumor formation. Indeed, MDMX amplification and/or overexpression occurs in several diverse tumors. Strikingly, recent work identifies MDMX as a specific chemotherapeutic target for treatment of retinoblastoma. Specific MDMX antagonists should therefore be developed as a tool to ensure activation of 'dormant' p53 activity in tumors that retain wild-type p53.
引用
收藏
页码:371 / 378
页数:8
相关论文
共 92 条
[1]   Repression of the Arf tumor suppressor by E2F3 is required for normal cell cycle kinetics [J].
Aslanian, A ;
Iaquinta, PJ ;
Verona, R ;
Lees, JA .
GENES & DEVELOPMENT, 2004, 18 (12) :1413-1422
[2]   MdmX is a RING finger ubiquitin ligase capable of synergistically enhancing Mdm2 ubiquitination [J].
Badciong, JC ;
Haas, AL .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2002, 277 (51) :49668-49675
[3]   MDM2 EXPRESSION IS INDUCED BY WILD TYPE-P53 ACTIVITY [J].
BARAK, Y ;
JUVEN, T ;
HAFFNER, R ;
OREN, M .
EMBO JOURNAL, 1993, 12 (02) :461-468
[4]  
Bartel F, 2004, MOL CANCER RES, V2, P29
[5]  
BOESTEN LS, 2006, CELL DEATH DIFFER, V13, P927
[6]   Comparative study of the p53-mdm2 and p53-MDMX interfaces [J].
Böttger, V ;
Böttger, A ;
Garcia-Echeverria, C ;
Ramos, YFM ;
van der Eb, AJ ;
Jochemsen, AG ;
Lane, DP .
ONCOGENE, 1999, 18 (01) :189-199
[7]   MOLECULAR ANALYSIS AND CHROMOSOMAL MAPPING OF AMPLIFIED GENES ISOLATED FROM A TRANSFORMED MOUSE 3T3-CELL LINE [J].
CAHILLYSNYDER, L ;
YANGFENG, T ;
FRANCKE, U ;
GEORGE, DL .
SOMATIC CELL AND MOLECULAR GENETICS, 1987, 13 (03) :235-244
[8]   ARF-BP1/mule is a critical mediator of the ARF tumor suppressor [J].
Chen, DL ;
Kon, N ;
Li, MY ;
Zhang, WZ ;
Qin, J ;
Gu, W .
CELL, 2005, 121 (07) :1071-1083
[9]   ATM and Chk2-dependent phosphorylation of MDMX contribute to p53 activation after DNA damage [J].
Chen, LH ;
Gilkes, DM ;
Pan, Y ;
Lane, WS ;
Chen, JD .
EMBO JOURNAL, 2005, 24 (19) :3411-3422
[10]   Regulation of p53-MDMX interaction by casein kinase 1 alpha [J].
Chen, LH ;
Li, CG ;
Pan, Y ;
Chen, JD .
MOLECULAR AND CELLULAR BIOLOGY, 2005, 25 (15) :6509-6520