Correlation of p53 oligomeric status and its subcellular localization in the presence of the AML-associated NPM mutant.
Ontology highlight
ABSTRACT: Tumor suppressor p53 is a key player in the cell response to DNA damage that suffers by frequent inactivating aberrations. Some of them disturb p53 oligomerization and influence cell decision between proliferation, growth arrest and apoptosis. Active p53 resides mostly in the nucleus, degradation occurs in the cytoplasm. Acute myeloid leukemia (AML)-related mutation of NPM (NPMmut) induces massive mislocalization of p53 to the cytoplasm, which might be related to leukemia initiation. Since both proteins interact and execute their function as oligomers, we investigated the role of perturbed p53 oligomerization in the p53 mislocalization process in live cells by FLIM (fluorescence lifetime imaging microscopy), fluorescence anisotropy imaging (FAIM), fluorescence cross-correlation spectroscop
SUBMITTER: Holoubek A
PROVIDER: S-EPMC12058200 | biostudies-literature | 2025
REPOSITORIES: biostudies-literature
ACCESS DATA