Fiel R J, Datta-Gupta N, Mark E H, Howard J C
Cancer Res. 1981 Sep;41(9 Pt 1):3543-5.
The photosensitizing effects of hematoporphyrin derivative, meso-tetra(p-sulfonatophenyl)porphine, meso-tetra(p-carboxyphenyl)porphine, and meso-tetra(4-N-methylpyridyl)-porphine on ColE1 supercoiled DNA were studied using agarose gel electrophoresis. Photoinduced single- and double-strand breaks were observed to form under neutral conditions. Singlet oxygen was shown to predominate in the mechanism of the induction of these lesions in the case of hematoporphyrin derivative, meso-tetra(p-sulfonatophenyl)porphine, and meso-tetra(p-carboxyphenyl)porphine and to play a significant role in the case of meso-tetra(4-N-methylpyridyl)porphine. The results suggest the possibility that the risk of photodynamic carcinogenesis may accompany photochemotherapy and fluorescence endoscopic procedures involving porphyrin photosensitizers.
利用琼脂糖凝胶电泳研究了血卟啉衍生物、中-四(对-磺酸钠苯基)卟啉、中-四(对-羧基苯基)卟啉和中-四(4-N-甲基吡啶基)卟啉对ColE1超螺旋DNA的光敏作用。在中性条件下观察到光诱导的单链和双链断裂形成。在血卟啉衍生物、中-四(对-磺酸钠苯基)卟啉和中-四(对-羧基苯基)卟啉的情况下,单线态氧在这些损伤诱导机制中占主导地位,而在中-四(4-N-甲基吡啶基)卟啉的情况下起重要作用。结果表明,光动力致癌风险可能伴随着涉及卟啉光敏剂的光化学疗法和荧光内镜检查程序。