首页> 外文期刊>International journal of toxicology >A paradigm shift is required for the risk assessment of potential human health after exposure to low level chemical exposures: a response to the toxicity testing in the 21st century report.
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A paradigm shift is required for the risk assessment of potential human health after exposure to low level chemical exposures: a response to the toxicity testing in the 21st century report.

机译:暴露于低水平化学物质暴露后对潜在人类健康的风险评估需要进行范式转换:对21世纪报告中毒性测试的回应。

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摘要

Chemicals are known to be associated with birth defects, cancer, cardiovascular diseases, immunological, reproductive, and neurological disorders. In response to recent reviews of limitations of current concepts and techniques for toxicity testing, this commentary challenges the paradigm that chemicals are directly responsible for DNA damage in the genomic-nuclear DNA in relevant cells of the human body. This challenge is not that mutations do not play roles in human-inherited or somatic diseases but that chemical exposures bring about disease end points by epigenetic mechanisms or by alterations in adult stem cell numbers in utero (ie, the Barker hypothesis) or postnatally, by selecting preexisting mutated cells. Classic concepts, that is, multistage, multimechanism process of carcinogenesis, stem cell theory of cancer, and newer and ignored concepts, such as cancer stem cells and cell-cell communication, will be used to support the view that the toxic effect of chemicals is mediated by nonmutagenic mechanisms at human relevant exposures.
机译:已知化学物质与出生缺陷,癌症,心血管疾病,免疫,生殖和神经系统疾病有关。为了回应对毒性测试当前概念和技术的局限性的最新评论,该评论对以下范式提出了挑战:化学物质直接导致人体相关细胞中基因组-核DNA中的DNA损伤。这个挑战不是突变不会在人类遗传性疾病或躯体疾病中发挥作用,而是化学暴露通过表观遗传机制或子宫内成年干细胞数量的变化(即巴克假说)或产后通过选择预先存在的突变细胞。经典的概念,即致癌作用的多阶段,多机理过程,癌症的干细胞理论,以及更新而被忽视的概念(例如癌症干细胞和细胞间的通讯)将被用来支持以下观点:化学物质的毒性作用是非致突变机制介导的人类相关暴露。

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