Abstract

Nickel compounds are an important class of environmental pollutants and carcinogens. Chronic exposure to nickel compounds has been connected with increased risks of numerous cancers, including lung and kidney cancers. But the precise mechanism by which nickel compounds exert their carcinogenic properties is not completely understood. In this study, kidney cancer cells namely human embryonic kidney 293-containing SV40 large T-antigen (HEK293T) and 786-0 were incubated with various concentrations of nickel chloride for 24 h before analysing the expression of three histone H3K27 methylation-modifying enzymes and H3K27me3 using quantitative real-time polymerase chain reaction, Western blot and immunofluorescence analyses. Our results showed that incubation of nickel chloride upregulated the expression of H3K27me3 demethylase jumonji domain-containing protein 3 (JMJD3) in kidney cancer cells, which was accompanied by the reduction in the protein level of H3K27me3. Enhanced demethylation of H3K27me3 may represent a novel mechanism underlying the carcinogenicity of nickel compounds.

Keywords

DemethylaseCarcinogenKidneyChemistryCancerCancer researchMolecular biologyHistoneBiologyBiochemistryEndocrinologyDNAGenetics

MeSH Terms

HEK293 CellsHistonesHumansJumonji Domain-Containing Histone DemethylasesKidneyKidney NeoplasmsMethylationNickelUp-Regulation

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Publication Info

Year
2014
Type
article
Volume
32
Issue
7
Pages
1286-1292
Citations
13
Access
Closed

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Cite This

Xiaoqiang Guo, Yanmin Zhang, Qiang Zhang et al. (2014). The regulatory role of nickel on H3K27 demethylase JMJD3 in kidney cancer cells. Toxicology and Industrial Health , 32 (7) , 1286-1292. https://doi.org/10.1177/0748233714552687

Identifiers

DOI
10.1177/0748233714552687
PMID
25427687

Data Quality

Data completeness: 81%