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含砷碳氢化合物:对 HepG2 细胞基因表达、表观遗传学和生物转化的影响。

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

机构信息

Institute of Nutritional Science, University of Potsdam, Arthur-Scheunert-Allee 114-116, 14558, Nuthetal, Germany.

Heinrich-Stockmeyer Foundation, Parkstraße 44-46, 49214, Bad Rothenfelde, Germany.

出版信息

Arch Toxicol. 2018 May;92(5):1751-1765. doi: 10.1007/s00204-018-2194-z. Epub 2018 Mar 30.

Abstract

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.

摘要

含砷烃(AsHCs)是在鱼类和藻类中发现的砷脂的一个亚组,在各种人类细胞系中引起显著的毒性作用,并对细胞能量水平有相当大的影响。然而,其作用机制尚不清楚。本研究通过 RT-qPCR 分析了两种 AsHCs(AsHC 332 和 AsHC 360)对人肝(HepG2)细胞中涵盖 DNA 修复、应激反应、细胞死亡、自噬和表观遗传学的 44 个基因表达的影响。两种 AsHCs 都影响了基因表达,但程度不同。在用 AsHC 360 处理后,核酸内切酶 1(FEN1)、着色性干皮病 A 互补蛋白(XPA)和(胞嘧啶-5)-甲基转移酶 3A(DNMT3A)的基因表达均呈现出时间和浓度依赖性变化,表明对基因组稳定性有影响。在随后对表观遗传标记物的分析中,在 72 小时内,AsHC 332 和 AsHC 360 均未对全基因组甲基化水平产生影响,而用 AsHC 360 孵育则增加了全基因组羟甲基化水平。通过高效液相色谱-质谱分析细胞提取物和细胞培养基,发现两种 AsHCs 都有相当大的生物转化。鉴定出的代谢物不仅包括两种 AsHCs 的相应硫代类似物,还包括几种含砷脂肪酸和脂肪醇,这有助于我们了解砷脂的生物转化机制。

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