Characterization and Quantitative Analysis of DNA Adducts Formed from Lower Chlorinated PCB-Derived Quinones

Polychlorinated biphenyls are wide pollutants readily detected in environmental and human specimens. DNA adduction occurs through the corresponding quinones. Polychlorinated biphenyls are first metabolized to arene oxides, which can be further oxidized to dihydroxy metabolites by microsomal cytochrome P450s. The catechol and hydroquinone products are further oxidized by peroxidases to quinones, which are electrophilic and capable of reacting with DNA to form adducts. DNA adduction is initiated by Michael addition preferentially to guanosine followed by stabilization through enolization. Another nucleophilic attack forms a five-membered ring, which aromatizes by dehydration to form the final adduct. This report describes the characterization and quantitative study of DNA adducts formed from lower chlorinated PCB-derived quinones. Quantitative study by HPLC/ESI-MS/MS and ³²P-postlabeling-HPLC gave the adduct levels in the range of 3-1200 adducts per 10⁸ nucleotides. These results demonstrate that increasing chlorine substitution is associated with lower yields of DNA adduct. Although ³²P-postlabeling is more sensitive than HPLC/ESI-MS/MS for the quantitative analysis of DNA adducts, modification levels were severely underestimated by the ³²P-postlabeling assay as compared to the HPLC/ESI-MS/MS assay.