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Mol Biol (Mosk) ; 57(4): 665-667, 2023.
Article in Russian | MEDLINE | ID: mdl-37528785

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.


Subject(s)
Leukemia, Promyelocytic, Acute , Humans , Leukemia, Promyelocytic, Acute/drug therapy , Leukemia, Promyelocytic, Acute/genetics , Leukemia, Promyelocytic, Acute/metabolism , Trans-Activators/genetics , Proto-Oncogene Proteins/genetics , Proto-Oncogene Proteins/metabolism , Tretinoin/pharmacology , Tretinoin/therapeutic use , Transcription Factors/genetics , Cell Differentiation
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