MDMX (MDM4), a Promising Target for p53 Reactivation Therapy and Beyond

被引:41
|
作者
Marine, Jean-Christophe [1 ,2 ]
Jochemsen, Aart G. [3 ]
机构
[1] VIB, Ctr Biol Dis, Lab Mol Canc Biol, B-3000 Leuven, Belgium
[2] KULeuven, Ctr Human Genet, Lab Mol Canc Biol, B-3000 Leuven, Belgium
[3] Leiden Univ, Med Ctr, Dept Mol Cell Biol, NL-2300 RA Leiden, Netherlands
来源
关键词
SMALL-MOLECULE INHIBITOR; MESSENGER-RNA; CONDITIONAL ALLELE; TUMOR-FORMATION; CELL-DEATH; DOMAIN; HDMX; OVEREXPRESSION; PHOSPHORYLATION; DEGRADATION;
D O I
10.1101/cshperspect.a026237
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
The MDMX protein was identified as a p53-interacting protein with a strong similarity to MDM2. Like Mdm2, Mdmx expression is essential for curbing p53 activity during embryonic development, indicating nonredundant functions of Mdmx and Mdm2. There is now a large body of evidence indicating that cancers frequently up-regulate MDMX expression as a means to dampen p53 tumor-suppressor function. Importantly, MDMX also shows p53-independent oncogenic functions. These data make MDMX an attractive therapeutic target for cancer therapy. Here, we summarize the mechanisms used by cancer cells to increase MDMX expression and promising pharmacological strategies to target MDMX in cancer-in particular, the recent findings that antisense oligonucleotides (ASOs) can be used to efficiently modulate MDMX messenger RNA (mRNA) splicing.
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页数:15
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