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Hydrazones as novel epigenetic modulators: Correlation between TET 1 protein inhibition activity and their iron(II) binding ability
M. Jakubek, Z. Kejík, R. Kaplánek, V. Antonyová, R. Hromádka, V. Šandriková, D. Sýkora, P. Martásek, V. Král,
Jazyk angličtina Země Spojené státy americké
Typ dokumentu časopisecké články, práce podpořená grantem
- MeSH
- chelátory železa chemická syntéza chemie toxicita MeSH
- dioxygenasy antagonisté a inhibitory chemie MeSH
- enzymatické testy MeSH
- epigeneze genetická účinky léků MeSH
- hydrazony chemická syntéza chemie toxicita MeSH
- inhibitory enzymů chemická syntéza chemie toxicita MeSH
- železo chemie MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
Ten-eleven translocation protein (TET) 1 plays a key role in control of DNA demethylation and thereby of gene expression. Dysregulation of these processes leads to serious pathological states such as oncological and neurodegenerative ones and thus TET 1 targeting is highly requested. Therefore, in this work, we examined the ability of hydrazones (acyl-, aroyl- and heterocyclic hydrazones) to inhibit the TET 1 protein and its mechanism of action. Inhibitory activity of hydrazones 1-7 towards TET 1 was measured. The results showed a high affinity of the tested chelators for iron(II). The study clearly showed a significant correlation between the chelator's affinity for iron(II) ions (represented by the binding constant) and TET 1 protein inhibitory activity (represented by IC50 values).
BIOCEV 1st Faculty of Medicine Charles University Průmyslová 595 252 50 Vestec Czech Republic
General University Hospital Prague U nemocnice 2 121 08 Prague 2 Czech Republic
Research and Development Center C2P s r o Jungmannova 101 503 51 Chlumec nad Cidlinou Czech Republic
Citace poskytuje Crossref.org
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- $a Jakubek, Milan $u BIOCEV, First Faculty of Medicine, Charles University, Průmyslová 595, 252 50 Vestec, Czech Republic; Department of Analytical Chemistry, Faculty of Chemical Engineering, University of Chemistry and Technology, Technická 5, 166 28 Prague 6, Czech Republic; Department of Paediatrics and Adolescent Medicine, First Faculty of Medicine, Charles University, Ke Karlovu 2, 121 08 Prague 2, Czech Republic.
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- $a Ten-eleven translocation protein (TET) 1 plays a key role in control of DNA demethylation and thereby of gene expression. Dysregulation of these processes leads to serious pathological states such as oncological and neurodegenerative ones and thus TET 1 targeting is highly requested. Therefore, in this work, we examined the ability of hydrazones (acyl-, aroyl- and heterocyclic hydrazones) to inhibit the TET 1 protein and its mechanism of action. Inhibitory activity of hydrazones 1-7 towards TET 1 was measured. The results showed a high affinity of the tested chelators for iron(II). The study clearly showed a significant correlation between the chelator's affinity for iron(II) ions (represented by the binding constant) and TET 1 protein inhibitory activity (represented by IC50 values).
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