2,4-Dimethylaniline generates phosphorylated histone H2AX in human urothelial and hepatic cells through reactive oxygen species produced by cytochrome P450 2E1

• Published in: Archives of toxicology 2018-10, Vol.92 (10), p.3093-3101
• Main Authors: Qi, Yonggang, Toyooka, Tatsushi, Kashiwagi, Hiroki, Yanagiba, Yukie, Koda, Shigeki, Ohta, Hisayoshi, Wang, Rui-Sheng
• Format: Article
• Language: English
• Subjects: Acetylcysteine; Amines; Antioxidants; Biomedical and Life Sciences; Biomedicine; Bladder; Bladder cancer; Cancer; Carcinogenicity; Carcinogens; Chemical plants; Cytochrome; Cytochrome P450; Cytochromes P450; Deoxyribonucleic acid; Disulfiram; DNA; DNA damage; Environmental Health; Exposure; Genotoxicity; Health risks; Histone H2A; Liver; Metabolism; Molecular Toxicology; Occupational exposure; Occupational health; Occupational Medicine/Industrial Medicine; Organic chemistry; Outbreaks; Oxygen; Personnel management; Pharmacology/Toxicology; Reactive oxygen species
• ISSN: 0340-5761; 1432-0738
• DOI: 10.1007/s00204-018-2289-6

The Japanese Ministry of Health, Labour, and Welfare recently reported an outbreak of bladder cancer among workers who handled aromatic amines in Japan. 2,4-dimethylaniline (2,4-DMA) is one of the chemicals that workers are considered to have the most opportunities to be exposed. Genotoxic events are known to be crucial steps in the initiation of cancer. However, studies on the genotoxicity of 2,4-DMA are limited, particularly studies investigating the mechanism behind the genotoxicity by 2,4-DMA are completely lacking. We examined genotoxic properties of 2,4-DMA using phosphorylated histone H2AX (γ-H2AX), a sensitive and reliable marker of DNA damage, in cultured human urothelial and hepatic cells. Our results clearly showed that 2,4-DMA at a concentration range of 1–10 mM generates γ-H2AX in both cell lines, indicating that 2,4-DMA is genotoxic. During mechanistic investigation, we found that 2,4-DMA boosts intracellular reactive oxygen species, an effect clearly attenuated by disulfiram, a strong inhibitor of cytochrome P450 2E1 (CYP2E1). In addition, CYP2E1 inhibitors and the antioxidant, N -acetylcysteine, also attenuated γ-H2AX generation following exposure to 2,4-DMA. Collectively, these results suggest that γ-H2AX is formed following exposure to 2,4-DMA via reactive oxygen species produced by CYP2E1-mediated metabolism. Continuous exposure to genotoxic aromatic amines such as 2,4-DMA over a long period of time may have contributed to the development of bladder cancer. Our results provide important insights into the carcinogenicity risk of 2,4-DMA in occupational bladder cancer outbreaks at chemical plants in Japan.