| Literature DB >> 27022975 |
Orit Karni-Schmidt1, Maria Lokshin1, Carol Prives1.
Abstract
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. Understanding the dysregulation of MDM2 and MDMX in human cancers and how they function either together or separately in tumorigenesis may improve methods of diagnosis and for assessing prognosis. Targeting the proteins themselves, or their regulators, may be a promising therapeutic approach to treating some forms of cancer.Entities:
Keywords: MDM2; MDMX; cancer; p53; tumorigenesis
Mesh:
Substances:
Year: 2016 PMID: 27022975 PMCID: PMC6028239 DOI: 10.1146/annurev-pathol-012414-040349
Source DB: PubMed Journal: Annu Rev Pathol ISSN: 1553-4006 Impact factor: 23.472