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Nongenotoxic (epigenetic) carcinogens: pesticides as an example. A critical review.

机译:非遗传毒性(表观遗传)致癌物:以农药为例。严格审查。

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The following groups of pesticides are considered in this review by supposed mechanisms of their carcinogenicity: hepatocarcinogenic pesticides, pesticides - peroxisome proliferators, pesticides as endocrine disruptors, goitrogenic pesticides, pesticides producing sustained cell proliferation and some others. With very rare exceptions, pesticides do not react with DNA directly and the mechanisms of their carcinogenicity are, in general, similar to those of other nongenotoxic (epigenetic) carcinogens, namely: promotion of spontaneous initiation, cytotoxicity with sustained cell proliferation, oxidative stress, formation of activated receptors and some others. Genotoxicity of pesticides varies from its complete absence (propiconazol as an example) to a very pronounced one (captafol) with remaining compounds in between. These two compounds demonstrate full correlation between genotoxicity and carcinogenicity (or their absence). Many pesticides give positive results in some tests for genotoxicity but these results are frequently controversial, not readily reproducible, or obtained only at toxic dose levels. The weak genotoxicity of the majority of pesticides is easily explainable by their rather severe testing before their introduction into practical use. The above mechanisms are threshold-based and therefore pesticides are regulated through NOEL/safety factor. There exist examples of lack of correlation between genotoxicity and carcinogenicity: some pesticides are genotoxic (although not strongly) but noncarcinogenic, others are considered as nongenotoxic but are strongly carcinogenic (chlorothalonil, acetochlor). The general scheme of the promoters' effect is presented in which an important role is attributed to the cytochrome P-450 induction (some pesticides are the cytochrome P-450 inducers), formation of reactive oxygen species and peroxitome proliferation. Teratogenesis Carcinog. Mutagen. 20:229-240, 2000. Copyright 2000 Wiley-Liss, Inc.
机译:在本综述中,根据其致癌性的推测机制考虑了以下几类农药:肝癌农药,农药-过氧化物酶体增殖剂,作为内分泌干扰物的农药,促甲状腺激素农药,产生持续细胞增殖的农药等。除极少数例外外,农药不会直接与DNA发生反应,其致癌性机制通常与其他非遗传毒性(表观遗传)致癌物相似,包括:促进自发启动,具有持续性细胞增殖的细胞毒性,氧化应激,激活受体的形成等。杀虫剂的遗传毒性从完全不存在(以丙环唑为例)到非常明显的一种(卡他酚),其余之间存在化合物。这两种化合物显示出遗传毒性和致癌性(或不存在)之间的完全相关性。许多杀虫剂在某些遗传毒性试验中给出了积极的结果,但这些结果经常引起争议,不容易重现,或者仅在有毒剂量下才能获得。大多数农药的弱基因毒性很容易通过在投入实际使用之前进行相当严格的测试来解释。以上机制是基于阈值的,因此农药通过NOEL /安全系数进行调节。在遗传毒性和致癌性之间缺乏相关性的例子:一些农药具有遗传毒性(虽然不是很强),但是没有致癌性,其他农药被认为具有非遗传毒性,但是具有很强的致癌性(百菌清,乙草胺)。提出了启动子作用的一般方案,其中重要的作用归因于细胞色素P-450的诱导(某些农药是细胞色素P-450的诱导剂),活性氧的形成和过氧化物酶的增殖。致癌作用。诱变剂。 20:229-240,2000。版权所有2000 Wiley-Liss,Inc.。

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