{"title":"Mode of action of dieldrin-induced liver tumors: application to human risk assessment.","authors":"James E Klaunig, Samuel M Cohen","doi":"10.1080/10408444.2024.2377208","DOIUrl":null,"url":null,"abstract":"<p><p>Dieldrin is an organochlorine insecticide that was widely used until 1970 when its use was banned because of its liver carcinogenicity in mice. Several long-term rodent bioassays have reported dieldrin to induce liver tumors in in several strains of mice, but not in rats. This article reviews the available information on dieldrin liver effects and performs an analysis of mode of action (MOA) and human relevance of these liver findings. Scientific evidence strongly supports a MOA based on CAR activation, leading to alterations in gene expression, which result in increased hepatocellular proliferation, clonal expansion leading to altered hepatic foci, and ultimately the formation of hepatocellular adenomas and carcinomas. Associative events include increased liver weight, centrilobular hypertrophy, increased expression of Cyp2b10 and its resulting increased enzymatic activity. Other associative events include alterations of intercellular gap junction communication and oxidative stress. Alternative MOAs are evaluated and shown not to be related to dieldrin administration. Weight of evidence shows that dieldrin is not DNA reactive, it is not mutagenic, and it is not genotoxic in general. Furthermore, activation of other pertinent nuclear receptors, including PXR, PPARα, AhR, and estrogen are not related to dieldrin-induced liver tumors nor is there liver cytotoxicity. In previous studies, rats, dogs, and non-human primates did not show increased cell proliferation or production of pre-neoplastic or neoplastic lesions following dieldrin treatment. Thus, the evidence strongly indicates that dieldrin-induced mouse liver tumors are due to CAR activation and are specific to the mouse, which are qualitatively not relevant to human hepatocarcinogenesis. Thus, there is no carcinogenic risk to humans. This conclusion is also supported by a lack of positive epidemiologic findings for evidence of liver carcinogenicity. Based on current understanding of the mode of action of dieldrin-induced liver tumors in mice, the appropriate conclusion is that dieldrin is a mouse specific liver carcinogen and it does not pose a cancer risk to humans.</p>","PeriodicalId":10869,"journal":{"name":"Critical Reviews in Toxicology","volume":null,"pages":null},"PeriodicalIF":5.7000,"publicationDate":"2024-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Critical Reviews in Toxicology","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1080/10408444.2024.2377208","RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2024/7/30 0:00:00","PubModel":"Epub","JCR":"Q1","JCRName":"TOXICOLOGY","Score":null,"Total":0}
引用次数: 0
Abstract
Dieldrin is an organochlorine insecticide that was widely used until 1970 when its use was banned because of its liver carcinogenicity in mice. Several long-term rodent bioassays have reported dieldrin to induce liver tumors in in several strains of mice, but not in rats. This article reviews the available information on dieldrin liver effects and performs an analysis of mode of action (MOA) and human relevance of these liver findings. Scientific evidence strongly supports a MOA based on CAR activation, leading to alterations in gene expression, which result in increased hepatocellular proliferation, clonal expansion leading to altered hepatic foci, and ultimately the formation of hepatocellular adenomas and carcinomas. Associative events include increased liver weight, centrilobular hypertrophy, increased expression of Cyp2b10 and its resulting increased enzymatic activity. Other associative events include alterations of intercellular gap junction communication and oxidative stress. Alternative MOAs are evaluated and shown not to be related to dieldrin administration. Weight of evidence shows that dieldrin is not DNA reactive, it is not mutagenic, and it is not genotoxic in general. Furthermore, activation of other pertinent nuclear receptors, including PXR, PPARα, AhR, and estrogen are not related to dieldrin-induced liver tumors nor is there liver cytotoxicity. In previous studies, rats, dogs, and non-human primates did not show increased cell proliferation or production of pre-neoplastic or neoplastic lesions following dieldrin treatment. Thus, the evidence strongly indicates that dieldrin-induced mouse liver tumors are due to CAR activation and are specific to the mouse, which are qualitatively not relevant to human hepatocarcinogenesis. Thus, there is no carcinogenic risk to humans. This conclusion is also supported by a lack of positive epidemiologic findings for evidence of liver carcinogenicity. Based on current understanding of the mode of action of dieldrin-induced liver tumors in mice, the appropriate conclusion is that dieldrin is a mouse specific liver carcinogen and it does not pose a cancer risk to humans.
狄氏剂是一种有机氯杀虫剂,曾被广泛使用,直到 1970 年才因其对小鼠肝脏的致癌性而被禁止使用。一些长期的啮齿动物生物测定报告称,狄氏剂可诱发多个品系小鼠的肝脏肿瘤,但不会诱发大鼠的肝脏肿瘤。本文回顾了有关狄氏剂对肝脏影响的现有资料,并对这些肝脏研究结果的作用模式(MOA)和与人类的相关性进行了分析。科学证据有力地支持基于 CAR 激活的作用方式,CAR 激活会导致基因表达的改变,从而导致肝细胞增殖、克隆扩增和肝脏病灶的改变,最终形成肝细胞腺瘤和肝癌。相关事件包括肝脏重量增加、小叶中心肥大、Cyp2b10 表达增加及其导致的酶活性增加。其他相关事件包括细胞间隙连接通信的改变和氧化应激。对替代性作用方式进行了评估,结果表明与服用狄氏剂无关。大量证据表明,狄氏剂不具有 DNA 反应性,不具有诱变性,一般也不具有遗传毒性。此外,其他相关核受体(包括 PXR、PPARα、AhR 和雌激素)的激活与狄氏剂诱发的肝肿瘤无关,也不存在肝细胞毒性。在以往的研究中,大鼠、狗和非人灵长类动物在经狄氏剂处理后,细胞增殖或产生肿瘤前病变或肿瘤病变的情况并没有增加。因此,有证据有力地表明,狄氏剂诱发的小鼠肝脏肿瘤是由于 CAR 激活引起的,而且是小鼠特有的,与人类肝癌的发生没有定性关系。因此,对人类没有致癌风险。这一结论也得到了流行病学研究结果的支持,即缺乏肝脏致癌的正面证据。根据目前对狄氏剂诱发小鼠肝脏肿瘤的作用模式的了解,适当的结论是狄氏剂是一种小鼠特异性肝致癌物,对人类不构成致癌风险。
期刊介绍:
Critical Reviews in Toxicology provides up-to-date, objective analyses of topics related to the mechanisms of action, responses, and assessment of health risks due to toxicant exposure. The journal publishes critical, comprehensive reviews of research findings in toxicology and the application of toxicological information in assessing human health hazards and risks. Toxicants of concern include commodity and specialty chemicals such as formaldehyde, acrylonitrile, and pesticides; pharmaceutical agents of all types; consumer products such as macronutrients and food additives; environmental agents such as ambient ozone; and occupational exposures such as asbestos and benzene.