Results 181 to 190 of about 7,268 (227)
Secondary Interaction Between MDMX and p53 Core Domain Inhibits p53 DNA Binding
The MDMX oncoprotein is an important regulator of tumor suppressor p53 activity during embryonic development. Despite sequence homology to the ubiquitin E3 ligase MDM2, MDMX depletion activates p53 without significant increase in p53 level, implicating a
Jiandong Chen, Ming Gao, Wade Borcherds
exaly +2 more sources
The Roles of MDM2 and MDMX in Cancer [PDF]
For more than 25 years, MDM2 and its homolog MDMX (also known as MDM4) have been shown to exert oncogenic activity. These two proteins are best understood as negative regulators of the p53 tumor suppressor, although they may have additional p53-independent roles.
Orit, Karni-Schmidt +2 more
exaly +3 more sources
MDMX Contains an Autoinhibitory Sequence Element [PDF]
Significance The protein MDMX is an important negative regulator of the tumor suppressor p53 in normal cells and can become a powerful oncogene. Previous studies on isolated protein fragments established that the N-terminal domain of MDMX binds tightly to the N-terminal domain of p53 and inhibits it.
Michal Bista, Alan R Fersht
exaly +3 more sources
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Modification of MDMX by sumoylation
Biochemical and Biophysical Research Communications, 2005MDMX is a homolog of MDM2 and is critical for regulating p53 function during mouse development. MDMX level is regulated by MDM2-mediated poly-ubiquitination, which results in its accelerated degradation after DNA damage or expression of ARF. In this report, we demonstrate that MDMX can be modified by conjugation to SUMO-1 both in vivo and in vitro.
Yu, Pan, Jiandong, Chen
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Targeting MDM2 and MDMX in Retinoblastoma
Current Cancer Drug Targets, 2007Retinoblastoma is the third most common form of cancer in infants, and metastatic retinoblastoma is lethal in approximately 90% of cases. Early detection and aggressive therapy has resulted in a 95% probability of survival for retinoblastoma patients in the United States.
Nikia A, Laurie +3 more
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European journal of medicinal chemistry, 2023
The function of the p53 protein is impaired by the overexpression of its negative regulator murine double minute 2 protein (MDM2) and homologous protein MDMX.
Hui Luo +8 more
semanticscholar +1 more source
The function of the p53 protein is impaired by the overexpression of its negative regulator murine double minute 2 protein (MDM2) and homologous protein MDMX.
Hui Luo +8 more
semanticscholar +1 more source
MDMX drives pre-leukaemia progression
Nature Reviews Cancer, 2021Ueda et al. report that overexpression of MDMX in pre-leukaemic stem cells provides these cells with a competitive advantage and promotes the progression of various pre-leukaemic conditions to acute myeloid leukaemia in several mouse models.
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The role of miRNAs in MDMX‐p53 interplay
Journal of Evidence-Based Medicine, 2021AbstractMicroRNAs (miRNAs) are endogenous noncoding RNAs of 19‐24 nucleotides in length and are tightly related to tumorigenesis and progression. Recent studies have demonstrated that the tumor suppressor p53 and its negative controller MDMX are regulated by miRNAs in different ways.
Dehua Yu +3 more
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64Cu-Labeled Stapled Peptide-Based Radiopharmaceuticals Targeting MDM2/MDMX for Pan-p53 Tumors.
Journal of Medicinal ChemistryThe development of ideal peptide-based radiopharmaceuticals faces critical bottlenecks, primarily due to limited cellular internalization and insufficient deep tissue penetration of peptide carriers.
Hao Tian +14 more
semanticscholar +1 more source
Mdm2 and MdmX: Partners in p53 Destruction
Cancer Research, 2021Abstract Mdm2 and MdmX are two closely related proteins that have been well-characterized as negative regulators of the tumor suppressor p53. Their interplay and especially respective roles in ubiquitination and subsequent degradation of p53 have lacked clarity. Yang and colleagues now demonstrate an obligate role for MdmX in recruitment
openaire +2 more sources

