首页> 外文期刊>Regulatory Toxicology and Pharmacology: RTP >Tetrahydrofuran-induced tumors in rodents are not relevant to humans: Quantitative weight of evidence analysis of mode of action information does not support classification of tetrahydrofuran as a possible human carcinogen
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Tetrahydrofuran-induced tumors in rodents are not relevant to humans: Quantitative weight of evidence analysis of mode of action information does not support classification of tetrahydrofuran as a possible human carcinogen

机译:啮齿动物中的四氢呋喃诱导的肿瘤与人类无关:行动信息模式的定量重量不支持四氢呋喃的分类作为可能的人类致癌物质

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摘要

Inhalation of tetrahydrofuran (THF) causes a marginal increase in the incidence of renal tumors in male rats and an increase in the incidence of liver tumors in female mice. Quantitative weight of evidence (QWoE) was applied to assess experimental support for biologically plausible modes of action (MoA) of tumor formation by THF and their human relevance. QWoE did not obtain support for a MoA to induce kidney tumors in male rats from THF exposure via alpha(2u)-globulin nephropathy, exacerbation of chronic progressive nephropathy (CPN), DNA-damage, or recurrent cytotoxicity but obtained moderate to good support for a constitutive androgen receptor (CAR)mediated MoA for the induction of liver tumors in female mice. Tumors as a consequence of CAR-activation are not considered relevant to humans. Considering the previous conclusion that the increases in kidney tumors in male rats are unlikely related to THF-exposure and the support for a CAR-mediated MoA in mice obtained here, these tumors should not be used as a basis for THF cancer classification.
机译:吸入四氢呋喃(THF)引起雄性大鼠肾肿瘤发病率的边际增加,雌性小鼠肝肿瘤发生率的增加。应用了数量的证据(QWOE),用于评估THF及其人类相关性的生物学似合理的作用(MOA)的实验载体。 QWOE没有获得MOA的支持,以通过α(2u)-globulin肾病,加重慢性渐进性肾病(CPN),DNA损伤或复发性细胞毒性,但是获得中度至关重要的肾脏肿瘤构成雄激素受体(轿车)介导的MOA用于诱导雌性小鼠的肝肿瘤。由于汽车激活的后果而言,肿瘤并不认为与人类有关。考虑到以前的结论:肾脏肿瘤中肾脏肿瘤的增加与THF暴露和在这里获得的小鼠中的汽车介导的MOA的载体不大,这些肿瘤不应作为THF癌症分类的基础。

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