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.

Keywords

DemethylaseAcute promyelocytic leukemiaDownregulation and upregulationCancer researchRetinoic acidHistoneTretinoinLeukemiaChemistryRetinoidBiologyImmunologyBiochemistryGene

MeSH Terms

AnimalsDrug ResistanceNeoplasmHistone DemethylasesHistonesHumansLeukemiaPromyelocyticAcuteMiceMiceInbred NODMiceSCIDNeoplasm ProteinsOkadaic AcidOncogene ProteinsFusionPhosphorylationRNA InterferenceRNASmall InterferingReceptorsRetinoic AcidRetinoic Acid Receptor alphaSignal TransductionTranscription FactorsTranscriptionGeneticTretinoinTumor CellsCultured

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Publication Info

Year
2013
Type
article
Volume
23
Issue
3
Pages
376-389
Citations
84
Access
Closed

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84
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0
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81
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Cite This

Marı́a Francisca Arteaga, Jan‐Henrik Mikesch, Jihui Qiu et al. (2013). The Histone Demethylase PHF8 Governs Retinoic Acid Response in Acute Promyelocytic Leukemia. Cancer Cell , 23 (3) , 376-389. https://doi.org/10.1016/j.ccr.2013.02.014

Identifiers

DOI
10.1016/j.ccr.2013.02.014
PMID
23518351
PMCID
PMC6812572

Data Quality

Data completeness: 90%