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BRD4 degradation blocks expression of MYC and multiple forms of stem cell resistance in Ph + chronic myeloid leukemia.
- Source :
-
American journal of hematology [Am J Hematol] 2022 Sep; Vol. 97 (9), pp. 1215-1225. Date of Electronic Publication: 2022 Jul 18. - Publication Year :
- 2022
-
Abstract
- In most patients with chronic myeloid leukemia (CML) clonal cells can be kept under control by BCR::ABL1 tyrosine kinase inhibitors (TKI). However, overt resistance or intolerance against these TKI may occur. We identified the epigenetic reader BRD4 and its downstream-effector MYC as growth regulators and therapeutic targets in CML cells. BRD4 and MYC were found to be expressed in primary CML cells, CD34 <superscript>+</superscript> /CD38 <superscript>-</superscript> leukemic stem cells (LSC), and in the CML cell lines KU812, K562, KCL22, and KCL22 <superscript>T315I</superscript> . The BRD4-targeting drug JQ1 was found to suppress proliferation in KU812 cells and primary leukemic cells in the majority of patients with chronic phase CML. In the blast phase of CML, JQ1 was less effective. However, the BRD4 degrader dBET6 was found to block proliferation and/or survival of primary CML cells in all patients tested, including blast phase CML and CML cells exhibiting the T315I variant of BCR::ABL1. Moreover, dBET6 was found to block MYC expression and to synergize with BCR::ABL1 TKI in inhibiting the proliferation in the JQ1-resistant cell line K562. Furthermore, BRD4 degradation was found to overcome osteoblast-induced TKI resistance of CML LSC in a co-culture system and to block interferon-gamma-induced upregulation of the checkpoint antigen PD-L1 in LSC. Finally, dBET6 was found to suppress the in vitro survival of CML LSC and their engraftment in NSG mice. Together, targeting of BRD4 and MYC through BET degradation sensitizes CML cells against BCR::ABL1 TKI and is a potent approach to overcome multiple forms of drug resistance in CML LSC.<br /> (© 2022 The Authors. American Journal of Hematology published by Wiley Periodicals LLC.)
- Subjects :
- Animals
Blast Crisis drug therapy
Cell Cycle Proteins
Cell Line, Tumor
Drug Resistance, Neoplasm
Fusion Proteins, bcr-abl
Humans
Mice
Protein Kinase Inhibitors pharmacology
Protein Kinase Inhibitors therapeutic use
Proto-Oncogene Proteins c-myc
Stem Cells
Transcription Factors genetics
Leukemia, Myelogenous, Chronic, BCR-ABL Positive drug therapy
Leukemia, Myelogenous, Chronic, BCR-ABL Positive genetics
Leukemia, Myelogenous, Chronic, BCR-ABL Positive metabolism
Nuclear Proteins genetics
Subjects
Details
- Language :
- English
- ISSN :
- 1096-8652
- Volume :
- 97
- Issue :
- 9
- Database :
- MEDLINE
- Journal :
- American journal of hematology
- Publication Type :
- Academic Journal
- Accession number :
- 35794848
- Full Text :
- https://doi.org/10.1002/ajh.26650