| Literature DB >> 27308631 |
Linshan Hu1, Haibo Zhang1, Johann Bergholz1, Shengnan Sun1, Zhi-Xiong Jim Xiao1.
Abstract
MDM2 (mouse double minute 2 homolog) and MDMX (double minute X human homolog, also known as MDM4) are critical negative regulators of tumor protein p53. Our recent work shows that MDMX binds to and promotes degradation of retinoblastoma protein (RB) in an MDM2-dependent manner. In a xenograft tumor growth mouse model, silencing of MDMX results in inhibition of p53-deficient tumor growth, which can be effectively reversed by concomitant RB silencing. Thus, MDMX exerts its oncogenic activity via suppression of RB.Entities:
Keywords: MDM2; MDMX; RB; p53
Year: 2016 PMID: 27308631 PMCID: PMC4905407 DOI: 10.1080/23723556.2015.1106635
Source DB: PubMed Journal: Mol Cell Oncol ISSN: 2372-3556