The arsenic-based cure of acute promyelocytic leukemia promotes cytoplasmic sequestration of PML and PML/RARA through inhibition of PML body recycling
| Autor: | Magnar Bjørås, Øystein Bruserud, Serhiy Pankiv, Rolf Bjerkvig, Anne Simonsen, Amra Grudic, Emma Lång, Stig Ove Bøe |
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| Rok vydání: | 2012 |
| Předmět: |
Acute promyelocytic leukemia
Cytoplasm Oncogene Proteins Fusion viruses Immunology SUMO protein Fluorescent Antibody Technique Antineoplastic Agents Promyelocytic Leukemia Protein Biochemistry Arsenicals Promyelocytic leukemia protein chemistry.chemical_compound Arsenic Trioxide Leukemia Promyelocytic Acute Tumor Cells Cultured medicine Humans Recycling Nuclear protein Arsenic trioxide Cell Nucleus biology Tumor Suppressor Proteins Cell Cycle Nuclear Proteins Sumoylation virus diseases Oxides Cell Biology Hematology Cell cycle medicine.disease Virology Nuclear Pore Complex Proteins Cell nucleus Retinoic acid receptor medicine.anatomical_structure chemistry Mutation biology.protein Cancer research Transcription Factors |
| Zdroj: | Blood. 120:847-857 |
| ISSN: | 1528-0020 0006-4971 |
| DOI: | 10.1182/blood-2011-10-388496 |
| Popis: | Arsenic in the form of arsenic trioxide (ATO) is used as a therapeutic drug for treatment of acute promyelocytic leukemia (APL). The mechanism by which this agent cures this disease was previously shown to involve direct interactions between ATO and the promyelocytic leukemia protein (PML), as well as accelerated degradation of the APL-associated fusion oncoprotein PML/retinoic acid receptor α (RARA). Here we investigated the fate of PML-generated nuclear structures called PML bodies in ATO-treated cells. We found that ATO inhibits formation of progeny PML bodies while it stabilizes cytoplasmic precursor compartments, referred to as cytoplasmic assemblies of PML and nucleoporins (CyPNs), after cell division. This block in PML body recycling is readily detected at pharmacologic relevant ATO concentrations (0.02-0.5μM) that do not cause detectable cell-cycle defects, and it does not require modification of PML by SUMOylation. In addition, PML and PML/RARA carrying mutations previously identified in ATO-resistant APL patients are impeded in their ability to become sequestered within CyPNs. Thus, ATO may inhibit nuclear activities of PML and PML/RARA in postmitotic cells through CyPN-dependent cytoplasmic sequestration. |
| Databáze: | OpenAIRE |
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