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Critical effective methods to detect genotoxic carcinogens and neoplasm-promoting agents.

机译:检测遗传毒性致癌物和肿瘤促进剂的关键有效方法。

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摘要

Neoplasia in fish can result from contamination of waters with carcinogens and promoters. Cancer in fish, therefore, is a possible indicator of cancer risk to man and serves as a guide to the need for preventive approaches involving improved means of waste disposal and environmental hygiene. Moreover, cancer in fish indicates that this important food source may be contaminated. Detection of genotoxic carcinogens to which fish are exposed can be achieved quickly and efficiently by carefully selected batteries of complementary in vitro and in vivo bioassays. One such battery consists of the Ames test, a reverse mutation assay in prokaryotic Salmonella typhimurium, and the Williams test, involving DNA repair in freshly explanted metabolically highly competent liver cells from diverse species, including humans. Determination of DNA-carcinogen adducts by varied techniques, including 32P-postlabeling, as well as DNA breakage, mammalian cell mutagenicity, chromosome aberrations, sister chromatid exchange, or cell transformation represent additional approaches, each with its own advantages and disadvantages. More research is needed on systems to apprehend neoplasm promoters, but tests to determine interruption of intercellular communications through gap junctions appear promising. Other approaches rely on measurement of enzymes such as ornithine decarboxylase and protein kinase C. Approaches to the definition of risk to fish or humans require characterization of the genotoxic or nongenotoxic properties of a chemical, relative potency data obtained in select, limited rodent bioassays, and knowledge of prevailing environmental concentrations of specific carcinogens.
机译:鱼中的肿瘤可能是由于水被致癌物和促进剂污染所致。因此,鱼中的癌症可能是人类罹患癌症风险的指标,并且可以指导人们采取预防措施,包括改善废物处理方式和环境卫生。此外,鱼中的癌症表明这种重要的食物来源可能受到污染。可以通过精心挑选的一系列补充的体外和体内生物测定方法,快速有效地检测出鱼类所接触的遗传毒性致癌物。一种这样的电池包括Ames试验,原核鼠伤寒沙门氏菌中的反向突变试验和Williams试验,该试验涉及对来自包括人类在内的各种物种的新鲜移植的代谢能力强的肝细胞进行DNA修复。通过多种技术测定DNA致癌物加合物,包括32P后标记以及DNA断裂,哺乳动物细胞诱变,染色体畸变,姐妹染色单体交换或细胞转化代表了其他方法,每种方法各有优缺点。需要进一步研究以了解肿瘤启动子的系统,但是通过间隙连接确定细胞间通讯中断的测试似乎很有希望。其他方法依赖于对酶的测量,如鸟氨酸脱羧酶和蛋白激酶C。定义鱼类或人的风险的方法需要表征化学的遗传毒性或非遗传毒性特性,在有限的啮齿动物生物测定中获得的相对效价数据以及了解特定致癌物的当前环境浓度。

著录项

  • 作者

    Weisburger, J H; Williams, G M;

  • 作者单位
  • 年度 1991
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  • 原文格式 PDF
  • 正文语种 {"code":"en","name":"English","id":9}
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