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本文引用的文献

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EVIDENCE FOR REPAIR OF ULTRA-VIOLET DAMAGED DEOXYRIBONUCLEIC ACID IN CULTURED MAMMALIAN CELLS.培养的哺乳动物细胞中紫外线损伤的脱氧核糖核酸修复的证据
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2
Use of unscheduled DNA synthesis in freshly isolated human intestinal mucosal cells for carcinogen detection.利用新分离的人肠黏膜细胞中的非程序性DNA合成进行致癌物检测。
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Metabolism of benzo[a]pyrene by cultured tracheobronchial tissues from mice, rats, hamsters, bovines and humans.小鼠、大鼠、仓鼠、牛和人类培养的气管支气管组织对苯并[a]芘的代谢
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Chemical carcinogen induction of DNA-repair synthesis in human peripheral blood monocytes.化学致癌物诱导人外周血单核细胞中的DNA修复合成。
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Use of primary cultures of adult rat hepatocytes on collagen gel-nylon mesh to evaluate carcinogen-induced unscheduled DNA synthesis.利用成年大鼠肝细胞原代培养物在胶原凝胶-尼龙网上评估致癌物诱导的非程序性DNA合成。
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Autoradiographic demonstration of DNA repair synthesis in rat tracheal epithelium treated with chemical carcinogen in vitro.体外化学致癌物处理的大鼠气管上皮细胞DNA修复合成的放射自显影证明
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Tumour production in glandular stomach of rat by N-methyl-N'-nitro-N-nitrosoguanidine.N-甲基-N'-硝基-N-亚硝基胍诱导大鼠腺胃肿瘤生成
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Invasive tumors induced in rats with actinomycin D.用放线菌素D在大鼠体内诱导产生的侵袭性肿瘤。
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DNA repair synthesis in mammalian cells exposed to a series of oncogenic and non-oncogenic derivatives of 4-nitroquinoline 1-oxide.暴露于4-硝基喹啉1-氧化物的一系列致癌和非致癌衍生物的哺乳动物细胞中的DNA修复合成。
Nature. 1971 Feb 5;229(5284):416-9. doi: 10.1038/229416a0.
10
Use of DNA repair synthesis in detecting organotropic actions of chemical carcinogens.利用DNA修复合成检测化学致癌物的器官亲和性作用。
Proc Soc Exp Biol Med. 1974 Apr;145(4):1339-42. doi: 10.3181/00379727-145-38009.

通过短期器官培养中大鼠气管上皮细胞非程序性DNA合成检测化学致癌物。

Detection of chemical carcinogens by assay of unscheduled DNA synthesis in rat tracheal epithelium in short-term organ culture.

作者信息

Ide F, Ishikawa T, Takayama S

出版信息

J Cancer Res Clin Oncol. 1981;102(2):115-26. doi: 10.1007/BF00410663.

DOI:10.1007/BF00410663
PMID:7338530
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12253380/
Abstract

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.

摘要

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。