The persistent organochlorine pesticide endosulfan modulates multiple epigenetic regulators with oncogenic potential in MCF-7 cells

被引:31
作者
Ghosh, Krishna [1 ]
Chatterjee, Biji [1 ]
Jayaprasad, Aparna Geetha [1 ]
Kanade, Santosh R. [1 ]
机构
[1] Cent Univ Kerala, Sch Biol Sci, Dept Biochem & Mol Biol, Kasaragod 671314, Kerala, India
关键词
alpha-Endosulfan; Epigenetics; Organochlorine pesticide; PRMT5; EZH2; HDAC; DNMT; HUMAN HACAT KERATINOCYTES; ESTROGEN-RECEPTOR; DNA METHYLATION; HISTONE DEACETYLASES; ARGININE METHYLATION; KINASE PATHWAYS; EZH2; EXPRESSION; ACTIVATION; BINDING; CANCER;
D O I
10.1016/j.scitotenv.2017.10.058
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Environmental cues and chemicals can potentially modulate the phenotypic expression of genome through alterations in the epigenetic mechanisms. Endosulfan is one of the extensively used organochlorine pesticides around the world which is known for its endocrine, neuro- and reproductive toxicity. This study was aimed to investigate the potential of alpha-endosulfan in modulation of multiple epigenetic enzymes in MCP-7 cells. The cells were treated with DMSO (control) or alpha-endosulfan (1 and 10 mu M) and the expression of various epigenetic enzymes was assayed by real-time PCR and immunoblotting, in addition to their activity assays. The results shows alpha-endosulfan, at 1 and 10 mu M concentration, significantly promoted viability of MCF-7 cells compared to untreated cells after 24 h. The expression of DNA methyltransferases (DNMTs) was upregulated while the global DNA methylation status was initially affected, but later recovered. Total intracellular histone deacetylase (HDAC) activity was found to be significantly increased which was correlated with upregulation of class I HDACs (HDAC 1 and 3) while no significant alteration in the other HDAC lasses was observed. The expression and activity of arginine and lysine methylation enzymes, protein arginine methyltransferase 5 (PRMT5) and Enhancer of Zeste homolog 2 (EZH2), respectively, were also found to be modulated by alpha-endosulfan. We found increased expression of histones H3 and H4, trimethylated H3K27 (product of EZH2), symmetric dimethylation of H4R3 (product of PRMT5) and five different (unidentified) proteins whose arginine residues are symmetrically dimethylated (by increased level of PRMT5) were enhanced in response to 10 mu M alpha-endosulfan after 24 h exposure window. Moreover. overexpression of basal level of estrogen receptor alpha (ER alpha), suggests estrogenicity of alpha-endosulfan. In summary, our results shows modulatory impact of alpha-endosulfan on multiple cellular epigenetic regulators, known to possess oncogenic potential which might contribute to mechanistic insight of its action in future. (C) 2017 Elsevier B.V. All rights reserved.
引用
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页码:1612 / 1622
页数:11
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