Abstract
All-trans retinoic acid (ATRA) in acute promyelocytic leukemia (APL) has been the most famous differentiation induction therapy during which the expression of PU.1, a key transcription factor (TF) for myeloid lineage determination in normal hematopoiesis is restored. In our previous studies, we found a stress-inducible H3K27 demethylase, JMJD3, to directly upregulate PU.1 expression to promote myeloid commitment during normal myelopoiesis. In addition, JMJD3 acts as an oncorepressor and plays a critical regulatory role in the initiation and progression of malignant hematopoiesis. In this study, we further resolved the relationship between JMJD3 and PU.1 in APL therein JMJD3 exerts oncorepressor activity via promoting PU.1 expression.
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The text was submitted by the author(s) in English.
The accession number for the raw data of RNA-seq and ChIP-seq reported in this paper is GEO: GSE101891. All other relevant data are available from the corresponding author on request.
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This work was supported by the National Natural Science Foundation of China (NSFC) (81900148), and Shanghai Rising-Star Program (20QC1400100).
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MXW, SHY, MX, and JC conducted the study design, data acquisition, and analyses. MXW, SHY, MX, and JC carried out the experiments and drafted the manuscript.
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Wang, MX., Yu, SH., Xiao, M. et al. JMJD3 Exerts Oncorepressor Activity in Acute Promyelocytic Leukemia by Promoting PU.1 Expression. Mol Biol 57, 653–660 (2023). https://doi.org/10.1134/S0026893323040179
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DOI: https://doi.org/10.1134/S0026893323040179