| Literature DB >> 30250876 |
Sonja Matt1, Thomas G Hofmann1.
Abstract
Tumor protein p53 (TP53, best known as p53), the most frequently mutated tumor suppressor in cancer, plays a central role in cell fate decisions induced by DNA damage. Regulation of p53 activity by post-translational modifications has been linked to promyelocytic leukemia nuclear bodies (PML-NBs), where p53 encounters many of its regulators. Recent evidence implies that crosstalk between p53 regulators at the PML-NB shapes post-translational modifications and function of p53.Entities:
Keywords: DNA damage; HIPK2; PML; SIRT1; apoptosis; crosstalk; nuclear body; p53
Year: 2018 PMID: 30250876 PMCID: PMC6150047 DOI: 10.1080/23723556.2015.1074335
Source DB: PubMed Journal: Mol Cell Oncol ISSN: 2372-3556