
The roles and regulation of MDM2 and MDMX: it is not just ...
Most well studied as proteins that restrain the p53 tumor suppressor protein, MDM2 and MDMX have rich lives outside of their relationship to p53. There is much to learn about how these two proteins are regulated and how they can function in cells that lack p53.
SLTE 2-23 lays the foundation for future force development ...
2023年3月6日 · MDMX, also referred to as “Mad Max,” is designed to test the MAGTF’s operational capabilities in austere, multi-domain, offensive and defensive operations against adversaries at a regimental...
MDM2 and MDMX: Alone and together in regulation of p53
In normal cells, MDM2 and MDMX suppress p53 activity, but in the event of cellular stress, they themselves must be inhibited so that p53 may respond to the stress. MDM2 and MDMX are known to bind together, and play multifaceted, non-redundant roles in …
MDMX (MDM4), a Promising Target for p53 Reactivation 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.
MDM2, MDMX and p53 in oncogenesis and cancer therapy
2013年1月10日 · The MDM2 and MDMX (also known as HDMX and MDM4) proteins are deregulated in many human cancers and exert their oncogenic activity predominantly by inhibiting the p53 tumour suppressor.
The Roles of MDM2 and MDMX in Cancer - PubMed
2016年5月23日 · 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 …
MDMX acts as a pervasive preleukemic-to-acute myeloid ...
2021年4月12日 · Our work identifies MDMX overexpression as a pervasive preleukemic-to-AML transition mechanism in different genetically driven disease subtypes, and reveals Wnt/β-Catenin as a non-canonical MDMX-driven pathway with therapeutic potential for progression prevention and cancer interception.