Interplay of RUNX1/MTG8 and DNA methyltransferase 1 in acute myeloid leukemia
Autor: | Chunhui Liu, Tamara Vukosavljevic, Jamie L. Ford, Christoph Plass, Laura J. Rush, Danilo Perrotti, John C. Byrd, Jianhua Yu, Lenguyen Huynh, Shujun Liu, Guido Marcucci, Marko I. Klisovic, Tiansheng Shen, Susan P. Whitman, Brian Becknell, Kun Sang Chang, Yu Li |
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Rok vydání: | 2005 |
Předmět: |
DNA (Cytosine-5-)-Methyltransferase 1
Cancer Research Methyltransferase Transcription Genetic Decitabine Biology Transfection Cell Line chemistry.chemical_compound RUNX1 Translocation Partner 1 Protein Transcriptional repressor complex hemic and lymphatic diseases Cell Line Tumor Proto-Oncogene Proteins medicine Humans DNA (Cytosine-5-)-Methyltransferases Gene Silencing Promoter Regions Genetic Depsipeptide Myeloid leukemia DNA Methylation Molecular biology DNA-Binding Proteins Gene Expression Regulation Neoplastic Oncology RUNX1 chemistry Leukemia Myeloid embryonic structures Acute Disease Core Binding Factor Alpha 2 Subunit DNMT1 Cancer research Interleukin-3 Chromatin immunoprecipitation medicine.drug Transcription Factors |
Zdroj: | Cancer research. 65(4) |
ISSN: | 0008-5472 |
Popis: | The translocation t(8;21)(q22;q22) in acute myeloid leukemia (AML) results in the expression of the fusion protein RUNX1/MTG8, which in turn recruits histone deacetylases (HDAC) to silence RUNX1 target genes [e.g., interleukin-3 (IL-3)].We previously reported that expression of the RUNX1/MTG8 target gene IL-3 is synergistically restored by the combination of inhibitors of HDACs (i.e., depsipeptide) and DNA methyltransferases (DNMT; i.e., decitabine) in RUNX1/MTG8-positive Kasumi-1 cells. Thus, we hypothesized that DNMT1 is also part of the transcriptional repressor complex recruited by RUNX1/MTG8. By a chromatin immunoprecipitation assay, we identified a RUNX1/MTG8-DNMT1 complex on the IL-3 promoter in Kasumi-1 cells and in primary RUNX1/MTG8-positive AML blasts. The physical association of RUNX1/MTG8 with DNMT1 was shown by coimmunoprecipitation experiments. Furthermore, RUNX1/MTG8 and DNMT1 were concurrently released from the IL-3 promoter by exposure to depsipeptide or stabilized on the promoter by decitabine treatment. Finally, we proved that RUNX1/MTG8 and DNMT1 were functionally interrelated by showing an enhanced repression of IL-3 after coexpression in 293T cells. These results suggest a novel mechanism for gene silencing mediated by RUNX1/MTG8 and support the combination of HDAC and DNMT inhibitors as a novel therapeutic approach for t(8;21) AML. |
Databáze: | OpenAIRE |
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