Arsenic-containing hydrocarbons: effects on gene expression, epigenetics, and biotransformation in HepG2 cells

被引:19
|
作者
Mueller, S. M. [1 ,2 ]
Finke, H. [1 ]
Ebert, F. [1 ]
Kopp, J. F. [1 ]
Schumacher, F. [1 ,3 ]
Kleuser, B. [1 ]
Francesconi, K. A. [4 ]
Raber, G. [4 ]
Schwerdtle, T. [1 ]
机构
[1] Univ Potsdam, Inst Nutr Sci, Arthur Scheunert Allee 114-116, D-14558 Nuthetal, Germany
[2] Heinrich Stockmeyer Fdn, Parkstr 44-46, D-49214 Bad Rothenfelde, Germany
[3] Univ Duisburg Essen, Dept Mol Biol, Hufelandstr 55, D-45122 Essen, Germany
[4] Graz Univ, NAWI Graz, Inst Chem, Univ Pl 1, A-8010 Graz, Austria
基金
奥地利科学基金会;
关键词
Arsenolipids; Gene expression; Arsenic-containing hydrocarbons; Global DNA methylation; Arsenic speciation; Metabolism; INHIBITS DNA METHYLTRANSFERASE; BASE EXCISION-REPAIR; METHYLATION PATTERNS; XPA PROTEIN; STEM-CELLS; 5-HYDROXYMETHYLCYTOSINE; ARSENOLIPIDS; MODEL; 5-METHYLCYTOSINE; DEMETHYLATION;
D O I
10.1007/s00204-018-2194-z
中图分类号
R99 [毒物学(毒理学)];
学科分类号
100405 ;
摘要
Arsenic-containing hydrocarbons (AsHCs), a subgroup of arsenolipids found in fish and algae, elicit substantial toxic effects in various human cell lines and have a considerable impact on cellular energy levels. The underlying mode of action, however, is still unknown. The present study analyzes the effects of two AsHCs (AsHC 332 and AsHC 360) on the expression of 44 genes covering DNA repair, stress response, cell death, autophagy, and epigenetics via RT-qPCR in human liver (HepG2) cells. Both AsHCs affected the gene expression, but to different extents. After treatment with AsHC 360, flap structure-specific endonuclease 1 (FEN1) as well as xeroderma pigmentosum group A complementing protein (XPA) and (cytosine-5)-methyltransferase 3A (DNMT3A) showed time- and concentration-dependent alterations in gene expression, thereby indicating an impact on genomic stability. In the subsequent analysis of epigenetic markers, within 72 h, neither AsHC 332 nor AsHC 360 showed an impact on the global DNA methylation level, whereas incubation with AsHC 360 increased the global DNA hydroxymethylation level. Analysis of cell extracts and cell media by HPLC-mass spectrometry revealed that both AsHCs were considerably biotransformed. The identified metabolites include not only the respective thioxo-analogs of the two AsHCs, but also several arsenic-containing fatty acids and fatty alcohols, contributing to our knowledge of biotransformation mechanisms of arsenolipids.
引用
收藏
页码:1751 / 1765
页数:15
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