Toth B, Patil K, Erickson J, Gannett P
Eppley Institute for Research in Cancer, University of Nebraska Medical Center, Omaha 68198, USA.
In Vivo. 1998 Jul-Aug;12(4):379-82.
Benzenediazonium sulfate (BD) was given to Swiss mice by 26 subcutaneous injections of 10 micrograms/g body weight at weekly intervals. The treatment gave rise to tumors of the subcutis. The tumor incidences in the treated groups were 42% in females and 26% in males. The corresponding tumor incidences in the untreated controls were 0% in females and 2% in males. Histopathologically, the neoplasms were classified as fibrosarcomas, rhabdomyosarcomas, and osteosarcomas of the subcutaneous tissue. BD is formed during the cytochrome P-450 catalyzed metabolism of the carcinogenic 1-(phenylazo)-2-hydroxynaphthalene (Sudan I, Solvent Yellow 14), which was used as a coloring agent for food and other materials in several countries. Further, BD is a metabolic breakdown product of different classes of nitrogen-nitrogen bond- containing chemicals. BD is the fourth benzenediazonium salt found to be carcinogenic in this laboratory.
将硫酸苯重氮盐(BD)以每周一次、每次10微克/克体重的剂量给瑞士小鼠进行26次皮下注射。这种处理引发了皮下肿瘤。处理组中雌性小鼠的肿瘤发生率为42%,雄性为26%。未处理对照组中雌性的相应肿瘤发生率为0%,雄性为2%。组织病理学上,这些肿瘤被分类为皮下组织的纤维肉瘤、横纹肌肉瘤和骨肉瘤。BD是在细胞色素P - 450催化致癌的1 -(苯基偶氮)- 2 - 羟基萘(苏丹红I,溶剂黄14)的代谢过程中形成的,苏丹红I在多个国家被用作食品和其他材料的着色剂。此外,BD是不同类含氮 - 氮键化学物质的代谢分解产物。BD是本实验室发现的第四种具有致癌性的苯重氮盐。