关于异丙烯的致癌物专著报告。

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引用次数: 1

摘要

美国国家毒理学计划对异丙苯进行了一项癌症评估,以确定其是否可能被列入致癌物报告(RoC)。癌症评估记录在RoC专著中,该专著在公共论坛上进行了同行评审。本专著由两部分组成:(第一部分)癌症评估,审查相关的科学信息,评估其质量,将RoC清单标准应用于科学信息,并提供国家毒物控制计划(NTP)对中华人民共和国中异丙苯的清单状态的建议,(第二部分)为中华人民共和国提出的物质概况,包含国家毒物控制计划(NTP)的清单状态建议,科学证据的摘要被认为是达成该决定的关键,以及关于属性,使用,生产,暴露的数据。以及联邦法规和指导方针,以减少对丙烯的接触。本专著提供了关于异丙苯的现有科学信息的评估,包括人类暴露和特性,处置和毒性动力学,实验动物的癌症研究,以及机制和其他相关效应的研究,包括相关的毒理学效应,遗传毒理学和致癌性机制。根据这一评估,国家毒理学规划建议,根据实验动物研究的充分证据,将异丙苯列为RoC中合理预期的人类致癌物,实验动物研究发现,异丙苯暴露会导致雄性和雌性小鼠的肺部肿瘤和雌性小鼠的肝脏肿瘤。几种提出的致癌机制支持在实验动物中观察到的肺和肝肿瘤与人类的相关性。具体来说,有证据表明人类和实验动物通过相似的代谢途径代谢孜然。此外,在cumene诱导的小鼠肺肿瘤中观察到K-ras癌基因和p53肿瘤抑制基因的突变,以及许多其他基因的表达改变,类似于在人类肺癌和其他癌症中发现的分子改变。
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Report on carcinogens monograph on cumene.
The National Toxicology Program conducted a cancer evaluation on cumene for possible listing in the Report on Carcinogens (RoC). The cancer evaluation is captured in the RoC monograph, which was peer reviewed in a public forum. The monograph consists of two components: (Part 1) the cancer evaluation, which reviews the relevant scientific information, assesses its quality, applies the RoC listing criteria to the scientific information, and provides the NTP recommendation for listing status for cumene in the RoC, and (Part 2) the substance profile proposed for the RoC, containing the NTP's listing status recommendation, a summary of the scientific evidence considered key to reaching that decision, and data on properties, use, production, exposure, and Federal regulations and guidelines to reduce exposure to cumene. This monograph provides an assessment of the available scientific information on cumene, including human exposure and properties, disposition and toxicokinetics, cancer studies in experimental animals, and studies of mechanisms and other related effects, including relevant toxicological effects, genetic toxicology, and mechanisms of carcinogenicity. From this assessment, the NTP recommended that cumene be listed as reasonably anticipated to be a human carcinogen in the RoC based on sufficient evidence from studies in experimental animals, which found that cumene exposure caused lung tumors in male and female mice and liver tumors in female mice. Several proposed mechanisms of carcinogenesis support the relevance to humans of the lung and liver tumors observed in experimental animals. Specifically, there is evidence that humans and experimental animals metabolize cumene through similar metabolic pathways. In addition, mutations of the K-ras oncogene and p53 tumor-suppressor gene observed in cumene-induced lung tumors in mice, along with altered expression of many other genes, resemble molecular alterations found in human lung and other cancers.
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Report on Carcinogens Monograph on 1-Bromopropane: RoC Monograph 01. Report on Carcinogens Monograph on Cumene: RoC Monograph 02. Report on carcinogens monograph on 1-bromopropane. Report on carcinogens monograph on cumene.
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