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Metabolism of Arsenic Trioxide in Acute Promyelocytic Leukemia Cells
Author(s) -
Khaleghian Ali,
Ghaffari Seyed H.,
Ahmadian Shahin,
Alimoghaddam Kamran,
Ghavamzadeh Ardeshir
Publication year - 2014
Publication title -
journal of cellular biochemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.028
H-Index - 165
eISSN - 1097-4644
pISSN - 0730-2312
DOI - 10.1002/jcb.24838
Subject(s) - arsenic trioxide , acute promyelocytic leukemia , methyltransferase , dna methylation , methylation , chemistry , glutathione , dnmt3b , dna methyltransferase , metabolism , biochemistry , metabolite , arsenic , microbiology and biotechnology , enzyme , apoptosis , biology , retinoic acid , dna , gene expression , gene , organic chemistry
Arsenic trioxide (As 2 O 3 ) effectively induces complete clinical and molecular remissions in acute promyelocytic leukemia (APL) patients and triggers apoptosis in APL cells. The effect induced by As 2 O 3 is also associated with extensive genomic‐wide epigenetic changes with large‐scale alterations in DNA methylation. We investigated the As 2 O 3 metabolism in association with factors involved in the production of its methylated metabolites in APL‐derived cell line, NB4. We used high performance liquid chromatography (HPLC) technique to detect As 2 O 3 metabolites in NB4 cells. The effects of As 2 O 3 on glutathione level, S ‐Adenosylmethionine (SAM) and S ‐adenosylhomocysteine (SAH) levels were investigated. Also, we studied the expression levels of arsenic methyltransferase (AS3MT) and DNA methyltransferases (DNMT1, DNMT3a, and DNMT3b) by real‐time PCR. Our results show that after As 2 O 3 entry into the cell, it was converted into methylated metabolites, mono‐methylarsenic (MMA) and dimethylarsenic (DMA). The glutathione (GSH) production was increased in parallel with the methylated metabolites formations. As 2 O 3 treatment inhibited DNMTs (DNMT1, DNMT3a, and DNMT3b) in dose‐ and time‐dependent manners. The SAH levels in As 2 O 3 ‐treated cells were increased; however, the SAM level was not affected. The present study shows that APL cell is capable of metabolizing As 2 O 3. The continuous formation of intracellular methylated metabolites, the inhibition of DNMTs expression levels and the increase of SAH level by As 2 O 3 biotransformation would probably affect the DNMTs‐methylated DNA methylation in a manner related to the extent of DNA hypomethylation. Production of intracellular methylated metabolites and epigenetic changes of DNA methylation during As 2 O 3 metabolism may contribute to the therapeutic effect of As 2 O 3 in APL. J. Cell. Biochem. 115: 1729–1739, 2014. © 2014 Wiley Periodicals, Inc.