Quantitative structure-toxicity relationships of halobenzoquinone isomers on DNA reactivity and genotoxicity

• Published in: Chemosphere (Oxford) 2022-12, Vol.309, p.136763-136763, Article 136763
• Main Authors: Tu, Nannan, Liu, Huan, Li, Wanling, Yao, Shuo, Liu, Juanli, Guo, Zhaoying, Yu, Rui, Du, Haiying, Li, Jinhua
• Format: Article
• Language: English
• Subjects: Disinfection byproducts; DNA interaction; Genotoxicity; Halobenzoquinones; Isomeric effects; Quantitative structure-toxicity relationship
• ISSN: 0045-6535; 1879-1298
• DOI: 10.1016/j.chemosphere.2022.136763

Halobenzoquinones (HBQs) are an emerging class of drinking water disinfection byproducts that have been predicted as bladder carcinogens. However, data on the genotoxicity of HBQs are still scarce. This study performed a quantitative structure-toxicity relationship (QSTR) analysis of HBQ isomers on DNA reactivity and genotoxicity. The interaction of HBQs with calf thymus DNA (ct-DNA) was studied using multi-spectroscopic and molecular docking techniques. UV–Vis absorption spectra observed a significant hyperchromic effect with the increase of HBQ concentration. The fluorescence intensity of both probe-ct-DNA decreased with the increasing concentration of HBQs, indicating that the interaction mode between each HBQs and DNA was quite complicated, and there were both minor groove binding and intercalation binding. Molecular docking showed that HBQs interacted with DNA predominantly via hydrogen bond at guanine-rich areas in the minor groove of DNA. The genotoxicity of HBQs on human hepatocytes (L-02) was evaluated by micronucleus test, and the results showed that HBQs could cause significant chromosomal damage. The rank order of HBQ isomers on DNA reactivity and genotoxicity was 2,5-HBQs > their corresponding 2,6-HBQs. QSTR analysis found that dipole moment is the key structural descriptor influencing both DNA reactivity and genotoxicity of HBQ isomers. This study suggested that HBQs have caused genotoxicity which was influenced by their isomeric effects, warranting a comprehensive understanding of the genotoxic and carcinogenic risks associated with HBQs exposure. [Display omitted] •HBQs interact with DNA through intercalative or minor groove binding.•HBQs could cause significant chromosomal damage.•The rank order of genotoxicity was 2,5-HBQs > their corresponding 2,6-HBQs.•Dipole moment is the key structural descriptor on genotoxicity of HBQ isomers.