根据动物癌症研究和机理数据,对甲基叔丁基醚的证据基础进行系统评估,证明不存在对人类致癌危险的担忧

IF 2.9 Q2 TOXICOLOGY
S.J. Borghoff , B.N. Rivera , S. Fitch , A.N. Buerger , N.Y. Choksi , A. Franzen , M.J. Vincent , T. Covington , J. Bus , E. Rushton , I.A. Lea
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引用次数: 0

摘要

甲基叔丁基醚(MTBE)是一种高辛烷值的燃料成分,有助于汽油燃烧更清洁,减少汽车排放。1999年,国际癌症研究机构(IARC)将MTBE归类为“不可分类”的人类致癌性。从那以后,又发表了更多的研究,大大增加了证据基础,以检验甲基叔丁基醚对人类的致癌潜力。我们进行了系统的文献检索和综述,以确定机制数据,以及研究mtbe暴露的人类和实验动物的癌症。在致癌物关键特征(KCCs)范围内组织和评估机制数据,对相关研究进行了批判性评估。三种标准动物癌症生物测定显示,雌性小鼠的肝细胞腺瘤(吸入暴露)发生率低,而雄性大鼠的肾腺瘤/癌(吸入)和脑瘤(饮用水)暴露于高浓度MTBE。从文献中提取的证据表明,雄性大鼠肾肿瘤的机制并不适用于人类。对机制数据强度的回顾是基于活性、相关性和可靠性,信息密集的kcc2是遗传毒性的,kcc10改变细胞增殖、细胞死亡和营养供应,共同支持MTBE不太可能对人类造成致癌危害。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Systematic evaluation of the evidence base on methyl tert-butyl ether supporting a lack of concern for carcinogenic hazard in humans based on animal cancer studies and mechanistic data
Methyl tert-butyl ether (MTBE) is a high-octane fuel component that helps gasoline burn cleaner and reduces automobile emissions. In 1999, the International Agency for Research on Cancer (IARC) categorized MTBE as “not classifiable” regarding human carcinogenicity. Since then, additional studies have been published that substantially added to the evidence base to examine the carcinogenic potential of MTBE in humans. A systematic literature search and review was conducted to identify mechanistic data, as well as studies investigating cancer in MTBE-exposed humans and experimental animals. Critical appraisal was performed for relevant studies with mechanistic data organized and evaluated within Key Characteristics of Carcinogens (KCCs). Three standard animal cancer bioassays showed a low incidence of hepatocellular adenomas in female mice (inhalation exposure), with renal adenomas/carcinoma (inhalation) and brain tumors (drinking water) in male rats exposed to high concentrations of MTBE. Evidence extracted from the literature demonstrate that the mechanism of male rat renal tumors does not operate in humans. Review of the strength of mechanistic data was based on activity, relevancy, and reliability, with information-dense KCC2—is genotoxic, and KCC10—alters cell proliferation, cell death, and nutrient supply, together supporting that MTBE is unlikely to be a carcinogenic hazard to humans.
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来源期刊
Current Research in Toxicology
Current Research in Toxicology Environmental Science-Health, Toxicology and Mutagenesis
CiteScore
4.70
自引率
3.00%
发文量
33
审稿时长
82 days
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