Shirai T, Nakamura A, Fukushima S, Tada M, Morita T, Ito N
First Department of Pathology, Nagoya City University Medical School, Japan.
Carcinogenesis. 1990 Apr;11(4):653-7. doi: 10.1093/carcin/11.4.653.
An immunohistochemical procedure was applied which allows accurate localization of DNA lesions within organs and tissues of rats given 3,2'-dimethyl-4-aminobiphenyl (DMAB) using polyclonal antibodies against DMAB-DNA adducts. Dose-related nuclear staining was observed in organs regardless of DMAB-carcinogenic organotropism. In the male accessory sex organs, the lateral lobe of the prostate, a non-target site, demonstrated a similar staining intensity to that found for the ventral prostate and seminal vesicle, target sites. Orchiectomy and pretreatment with ethinyl estradiol resulted in a moderate to slight decrease in binding in the accessory sex organs. No observable decrease in staining intensity was evident in most organs 168 h after the administration of DMAB. These findings suggest that DNA adduct formation itself is not necessarily sufficient for tumor induction.
应用了一种免疫组织化学方法,该方法使用针对二甲基氨基联苯(DMAB)-DNA加合物的多克隆抗体,能够在给予3,2'-二甲基-4-氨基联苯(DMAB)的大鼠的器官和组织内准确地定位DNA损伤。在各器官中均观察到与剂量相关的核染色,而与DMAB致癌的器官嗜性无关。在雄性附属性器官中,前列腺外侧叶作为一个非靶位点,其染色强度与作为靶位点的腹侧前列腺和精囊相似。睾丸切除术和用乙炔雌二醇预处理导致附属性器官中的结合有中度到轻度的降低。给予DMAB 168小时后,大多数器官中未观察到染色强度有明显降低。这些发现表明,DNA加合物的形成本身不一定足以诱发肿瘤。