1. The Histone Demethylase PHF8 Governs Retinoic Acid Response in Acute Promyelocytic Leukemia
- Author
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Arteaga, Maria Francisca, Mikesch, Jan-Henrik, Qiu, Jihui, Christensen, Jesper, Helin, Kristian, Kogan, Scott C, Dong, Shuo, and So, Chi Wai Eric
- Subjects
Biochemistry and Cell Biology ,Biological Sciences ,Pediatric ,Orphan Drug ,Childhood Leukemia ,Pediatric Cancer ,Cancer ,Rare Diseases ,Hematology ,2.1 Biological and endogenous factors ,5.1 Pharmaceuticals ,Animals ,Drug Resistance ,Neoplasm ,Histone Demethylases ,Histones ,Humans ,Leukemia ,Promyelocytic ,Acute ,Mice ,Mice ,Inbred NOD ,Mice ,SCID ,Neoplasm Proteins ,Okadaic Acid ,Oncogene Proteins ,Fusion ,Phosphorylation ,RNA Interference ,RNA ,Small Interfering ,Receptors ,Retinoic Acid ,Retinoic Acid Receptor alpha ,Signal Transduction ,Transcription Factors ,Transcription ,Genetic ,Tretinoin ,Tumor Cells ,Cultured ,Neurosciences ,Oncology and Carcinogenesis ,Oncology & Carcinogenesis ,Biochemistry and cell biology ,Oncology and carcinogenesis - Abstract
While all-trans retinoic acid (ATRA) treatment in acute promyelocytic leukemia (APL) has been the paradigm of targeted therapy for oncogenic transcription factors, the underlying mechanisms remain largely unknown, and a significant number of patients still relapse and become ATRA resistant. We identified the histone demethylase PHF8 as a coactivator that is specifically recruited by RARα fusions to activate expression of their downstream targets upon ATRA treatment. Forced expression of PHF8 resensitizes ATRA-resistant APL cells, whereas its downregulation confers resistance. ATRA sensitivity depends on the enzymatic activity and phosphorylation status of PHF8, which can be pharmacologically manipulated to resurrect ATRA sensitivity to resistant cells. These findings provide important molecular insights into ATRA response and a promising avenue for overcoming ATRA resistance.
- Published
- 2013