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Abstract
4-Hydrazinobenzoic acid, an ingredient of mushroom Agaricus bisporus, is carcinogenic to rodents. To clarify the mechanism of carcinogenesis, we investigated DNA damage by 4-hydrazinobenzoic acid using 32P-labeled DNA fragments obtained from the human p53 and p16 tumor suppressor genes. 4-Hydrazinobenzoic acid induced Cu(II)-dependent DNA damage especially piperidine-labile formation at thymine and cytosine residues. Typical hydroxyl radical scavengers showed no inhibitory effects on Cu(II)-mediated DNA damage by 4-hydrazinobenzoic acid. Bathocuproine and catalase inhibited the DNA damage, indicating the participation of Cu(I) and H2O2 in the DNA damage. These findings suggest that H2O2 generated by the autoxidation of 4-hydrazinobenzoic acid reacts with Cu(I) to form reactive oxygen species, capable of causing DNA damage. Interestingly, catalase did not completely inhibit DNA damage caused by a high concentration of 4-hydrazinobenzoic acid (over 50 μM) in the presence of Cu(II). 4-Hydrazinobenzoic acid induced piperidine-labile sites frequently at adenine and guanine residues in the presence of catalase. 4-Hydrazinobenzoic acid increased formation of 8-oxo-7,8-dihydro-2′-deoxyguanosine (8-oxodG), a characteristic oxidative DNA lesion, in calf thymus DNA, whereas 4-hydrazinobenzoic acid did not increase the formation of 8-oxodG in the presence of catalase. ESR spin-trapping experiments showed that the phenyl radical was formed during the reaction of 4-hydrazinobenzoic acid in the presence of Cu(II) and catalase. Matrix-assisted laser desorption/ionization time-of-flight mass (MALDI-TOF/mass) spectrometry analysis showed that phenyl radical formed adduct with adenosine and guanosine. These results suggested that 4-hydrazinobenzoic acid induced DNA damage via not only H2O2 production but also phenyl radical production. This study suggests that both oxidative DNA damage and DNA adduct formation play important roles in the expression of carcinogenesis of 4-hydrazinobenzoic acid.
| Abbreviations | ||
| 8-oxodG | = | 8-oxo-7,8-dihydro-2′-deoxyguanosine |
| DTPA | = | diethylenetriamine-N,N,N′,N″,N″-pentaacetic acid |
| SOD | = | superoxide dismutase |
| H2O2 | = | hydrogen peroxide |
| HPLC | = | high-performance liquid chromatography |
| HPLC-ECD | = | electrochemical detector coupled to HPLC |
| √OH | = | hydroxyl free radical |
| DMSO | = | dimetyl sulfate |
| ESR | = | electron spin resonance |
| MALDI-TOF/mass | = | matrix-assisted laser desorption/ionization time-of-flight mass spectrometry |
| Abbreviations | ||
| 8-oxodG | = | 8-oxo-7,8-dihydro-2′-deoxyguanosine |
| DTPA | = | diethylenetriamine-N,N,N′,N″,N″-pentaacetic acid |
| SOD | = | superoxide dismutase |
| H2O2 | = | hydrogen peroxide |
| HPLC | = | high-performance liquid chromatography |
| HPLC-ECD | = | electrochemical detector coupled to HPLC |
| √OH | = | hydroxyl free radical |
| DMSO | = | dimetyl sulfate |
| ESR | = | electron spin resonance |
| MALDI-TOF/mass | = | matrix-assisted laser desorption/ionization time-of-flight mass spectrometry |