Borghoff S J, Rivera B N, Fitch S, Buerger A N, Choksi N Y, Franzen A, Vincent M J, Covington T, Bus J, Rushton E, Lea I A
ToxStrategies, Durham, NC, United States.
ToxStrategies, Asheville, NC, United States.
Curr Res Toxicol. 2025 Feb 16;8:100224. doi: 10.1016/j.crtox.2025.100224. eCollection 2025.
Methyl -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.
甲基叔丁基醚(MTBE)是一种高辛烷值燃料成分,有助于汽油更清洁地燃烧并减少汽车尾气排放。1999年,国际癌症研究机构(IARC)将MTBE的人类致癌性归类为“无法分类”。从那时起,又发表了更多研究,极大地扩充了用于检验MTBE对人类致癌潜力的证据库。开展了一项系统的文献检索和综述,以识别机制数据,以及调查MTBE暴露人群和实验动物癌症情况的研究。对相关研究进行了批判性评估,将机制数据按照致癌物关键特性(KCCs)进行组织和评估。三项标准动物癌症生物测定显示,雌性小鼠(吸入暴露)肝细胞腺瘤发病率较低,高浓度MTBE暴露的雄性大鼠出现肾腺瘤/癌(吸入)和脑肿瘤(饮水)。从文献中提取的证据表明,雄性大鼠肾肿瘤的发生机制在人类中并不起作用。对机制数据强度的综述基于活性、相关性和可靠性,信息密集的KCC2(具有遗传毒性)和KCC10(改变细胞增殖、细胞死亡和营养供应)共同支持MTBE对人类不太可能构成致癌风险。