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MDM1 — TP53
Text-mined interactions from Literome
Yu et al., Oncogene 2000
:
In the current study,
MDM2 mediated degradation of
p53 was partially inhibited in cells treated with leptomycin B ( LMB ), a specific inhibitor of nuclear export
Inoue et al., FEBS Lett 2001
:
Importantly,
MDM2 overexpression
inhibited the stabilization of
p53 and decrease in ubiquitination following MMC, MMS, and UV treatment
Gu et al., Blood 2002
(Precursor Cell Lymphoblastic Leukemia-Lymphoma) :
In the presence of wild-type ( wt )
p53 ,
MDM2 increased p65 promoter activity by reversing p53 mediated suppression of p65 ... In the absence of
p53 ,
MDM2 directly
increased p65 promoter activity
Jin et al., J Biol Chem 2002
:
Consistent with the above results,
MDM2 significantly
repressed the activation of
p53 transcriptional activity by PCAF without apparently affecting the level of p53
Wei et al., J Biol Chem 2003
(Osteosarcoma) :
In contrast,
MDM2 inhibits
p53 by promoting its degradation
Ko et al., Oncogene 2003
(Cell Transformation, Neoplastic...) :
In HCCR-2 transfected NCI-H460 cells and RKO cells, stabilization of the p53 tumor suppressor occurred without genetic mutation and correlated with functional impairment, as indicated by the defective induction of
p53 induced p21 ( WAF1 ),
MDM2 , and bax
Zhao et al., J Biol Chem 2004
:
Interestingly, whereas Daxx did not bind to p53 in cells as assessed by immunoprecipitation,
MDM2 expression
restored p53-Daxx interaction, and this correlated with deacetylation of p53
Lin et al., Oncogene 2005
(Bone Neoplasms...) :
Overexpressed myc tagged topors associates with and stabilizes p53, and enhances the
p53 dependent transcriptional activities of p21 ( Waf1 ),
MDM2 and Bax promoters and elevates endogenous p21 ( Waf1 ) mRNA levels
Wiederschain et al., J Biol Chem 2005
(Translocation, Genetic) :
Our data show that MLL-AF9, MLL-AF10, MLL-ENL, and MLL-ELL substantially down-regulate
p53 mediated
induction of p21,
MDM2 , and Bax in response to DNA damage
Wang et al., EMBO J 2005
:
Therefore,
MDM2 interaction with KAP1
contributes to
p53 functional regulation
Toledo et al., Int J Biochem Cell Biol 2007
(Neoplasms) :
We now know that MDM2 and MDM4 inhibit p53 in distinct and complementary ways
: MDM4 regulates
p53 activity, while MDM2 mainly regulates p53 stability
Phang et al., Eur J Cancer 2008
(Leukemia) :
Although mutations in p53 are rare in leukaemia,
MDM2 , the negative
regulator of
p53 , is often overexpressed
Markey et al., Frontiers in bioscience (Landmark edition) 2011
(Neoplasms) :
Under normal growth conditions,
MDM4 contributes to the repression of
p53 activity
Vaughan et al., Genes & cancer 2011
:
Consistently, analysis of functional domains of MDM2 indicated that although the p53-interaction domain of MDM2 contributes to the up-regulation of the NF?B2 promoter,
MDM2 does not
require direct interactions with
p53 for this function