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首页> 外文期刊>Toxicological sciences: An official journal of the Society of Toxicology >Chemically exacerbated chronic progressive nephropathy not associated with renal tubular tumor induction in rats: An evaluation based on 60 carcinogenicity studies by the national toxicology program
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Chemically exacerbated chronic progressive nephropathy not associated with renal tubular tumor induction in rats: An evaluation based on 60 carcinogenicity studies by the national toxicology program

机译:与大鼠肾小管肿瘤诱发无关的化学加重性慢性进行性肾病:基于国家毒理学计划的60项致癌性研究的评估

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摘要

Chronic progressive nephropathy (CPN) is a common age-related degenerative-regenerative disease of the kidney that occurs in both sexes of most strains of rats. Recently, claims have been made that enhanced CPN is a mode of action for chemically induced kidney tumors in male rats and that renal tubular tumors (RTTs) induced by chemicals that concomitantly exacerbate CPN are not relevant for human cancer risk assessments. Although CPN is an observable histopathological lesion that may be modified by diet, the etiology of this disease and the mechanisms for its exacerbation by chemicals are unknown, and it fails to meet fundamental principles for defining carcinogenic modes of action and human relevance. Our comprehensive evaluation of possible relationships between exacerbated CPN and induction of RTTs in 58 carcinogenicity studies, conducted by the National Toxicology Program, in male and 11 studies in female F344 rats using 60 chemicals revealed widespread inconsistency in the claimed association. Because the proposed hypothesis lacks evidence of biological plausibility, and due to inconsistent relationships between exacerbated CPN and kidney tumor incidence in carcinogenicity studies in rats, dismissing the human relevance of kidney tumors induced by chemicals that also exacerbate CPN in rats would be wrong.
机译:慢性进行性肾病(CPN)是一种常见的年龄相关性肾脏退行性再生疾病,在大多数大鼠品系的男性和女性中均会发生。最近,有人声称增强的CPN是雄性大鼠化学诱导的肾脏肿瘤的一种作用方式,而化学药品诱发的肾小管肿瘤(RTT)会同时加重CPN与人类癌症风险评估无关。尽管CPN是一种可通过饮食改变的可观察到的组织病理学病变,但该病的病因及其由化学物质加剧的机制尚不清楚,并且它不能满足定义致癌作用模式和人类相关性的基本原则。我们对由国家毒理学计划进行的58项致癌性研究中CPN恶化与RTT诱导之间可能关系的综合评估,在雄性和雌性F344大鼠的11项研究中,使用了60种化学物质,表明在所声称的关联中普遍存在不一致之处。由于所提出的假设缺乏生物学上的合理性证据,并且由于大鼠致癌性研究中加重的CPN与肾脏肿瘤发生率之间的关系不一致,因此认为化学物质加重大鼠CPN导致人与肾脏肿瘤的相关性被认为是错误的。

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