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草甘膦对人外周血单个核细胞诱导的DNA损伤和甲基化(体外研究)

DNA damage and methylation induced by glyphosate in human peripheral blood mononuclear cells (in vitro study).

作者信息

Kwiatkowska Marta, Reszka Edyta, Woźniak Katarzyna, Jabłońska Ewa, Michałowicz Jaromir, Bukowska Bożena

机构信息

Department of Biophysics of Environmental Pollution, Faculty of Biology and Environmental Protection, University of Lodz, Lodz, Poland.

Department of Molecular Genetics and Epigenetics, Nofer Institute of Occupational Medicine, Lodz, Poland.

出版信息

Food Chem Toxicol. 2017 Jul;105:93-98. doi: 10.1016/j.fct.2017.03.051. Epub 2017 Mar 27.

Abstract

Glyphosate is a very important herbicide that is widely used in the agriculture, and thus the exposure of humans to this substance and its metabolites has been noted. The purpose of this study was to assess DNA damage (determination of single and double strand-breaks by the comet assay) as well as to evaluate DNA methylation (global DNA methylation and methylation of p16 (CDKN2A) and p53 (TP53) promoter regions) in human peripheral blood mononuclear cells (PBMCs) exposed to glyphosate. PBMCs were incubated with the compound studied at concentrations ranging from 0.1 to 10 mM for 24 h. The study has shown that glyphosate induced DNA lesions, which were effectively repaired. However, PBMCs were unable to repair completely DNA damage induced by glyphosate. We also observed a decrease in global DNA methylation level at 0.25 mM of glyphosate. Glyphosate at 0.25 mM and 0.5 mM increased p53 promoter methylation, while it did not induce statistically significant changes in methylation of p16 promoter. To sum up, we have shown for the first time that glyphosate (at high concentrations from 0.5 to 10 mM) may induce DNA damage in leucocytes such as PBMCs and cause DNA methylation in human cells.

摘要

草甘膦是一种非常重要的除草剂,在农业中广泛使用,因此人们已注意到人类会接触到这种物质及其代谢产物。本研究的目的是评估草甘膦暴露后人外周血单个核细胞(PBMC)中的DNA损伤(通过彗星试验测定单链和双链断裂)以及评估DNA甲基化(整体DNA甲基化以及p16(CDKN2A)和p53(TP53)启动子区域的甲基化)。将PBMC与浓度范围为0.1至10 mM的所研究化合物孵育24小时。研究表明,草甘膦会诱导DNA损伤,这些损伤可得到有效修复。然而,PBMC无法完全修复草甘膦诱导的DNA损伤。我们还观察到,在0.25 mM草甘膦浓度下整体DNA甲基化水平降低。0.25 mM和0.5 mM的草甘膦会增加p53启动子甲基化,而对p16启动子甲基化未诱导出具有统计学意义的变化。总之,我们首次表明草甘膦(0.5至10 mM的高浓度)可能会诱导PBMC等白细胞中的DNA损伤并导致人类细胞中的DNA甲基化。

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