Ide F, Ishikawa T, Takayama S
J Cancer Res Clin Oncol. 1981;102(2):115-26. doi: 10.1007/BF00410663.
A short-term organ culture of rat tracheal epithelium was used to detect the ability of 53 chemicals to induce UDS. In this system all direct-acting compounds (ultimate or proximate carcinogens) tested induced UDS. Of 24 compounds requiring metabolism (procarcinogens), nine induced UDS, viz., 4NQO, AF-2, BP, DMN, DEN, and NP. Urethane, AAF, and 2,7-AAF induced very slight UDS. 3-Methyl-4NQO for which carcinogenicity data is incomplete as positive in our system. Among the cancer chemotherapeutic agents tested only mitomycin C induced UDS. MC and DMBA, which are known to induce cancer of respiratory organs in experimented animals, and DAB, aflatoxin B1 and Trp-P-1, which are strong carcinogens in the liver, did not induce UDS within 2 h. With the longer exposure (24 h), these carcinogens also failed to elicit UDS. All the carcinogens that induce UDS showed clear dose-dependent effects. No non-carcinogens tested induced UDS. These results suggested that this system should be useful for screening environmental chemicals suspected of damaging DNA of the respiratory organ on the basis of organotropic effects for UDS induction in cultured rat tracheal epithelium.
采用大鼠气管上皮短期器官培养法检测53种化学物质诱导非程序DNA合成(UDS)的能力。在该系统中,所有受试的直接作用化合物(终致癌物或近致癌物)均能诱导UDS。在24种需经代谢的化合物(前致癌物)中,9种可诱导UDS,即4-硝基喹啉-N-氧化物(4NQO)、AF-2、苯并芘(BP)、二甲基亚硝胺(DMN)、二乙基亚硝胺(DEN)和2-萘胺(NP)。氨基甲酸乙酯、黄曲霉毒素AF、2,7-黄曲霉毒素AF诱导的UDS非常轻微。致癌性数据不完整的3-甲基-4NQO在我们的系统中呈阳性。在所测试的癌症化疗药物中,只有丝裂霉素C诱导UDS。已知可在实验动物中诱发呼吸器官癌症的丝裂霉素C和二甲基苯蒽(DMBA),以及在肝脏中为强致癌物的二氨基联苯(DAB)、黄曲霉毒素B1和色氨酸-P-1,在2小时内均未诱导UDS。延长暴露时间(24小时)后,这些致癌物也未能引发UDS。所有诱导UDS的致癌物均表现出明显的剂量依赖性效应。所测试的非致癌物均未诱导UDS。这些结果表明,基于培养的大鼠气管上皮中UDS诱导的器官特异性效应,该系统可用于筛选怀疑会损害呼吸器官DNA的环境化学物质。