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整合毒性终点数据以提高化学品安全性评估的准确性:以致癌性评估为例。

Integration of data across toxicity endpoints for improved safety assessment of chemicals: the example of carcinogenicity assessment.

机构信息

European Commission, Joint Research Centre (JRC), Via E. Fermi 2749, 21027, Ispra, VA, Italy.

出版信息

Arch Toxicol. 2021 Jun;95(6):1971-1993. doi: 10.1007/s00204-021-03035-x. Epub 2021 Apr 8.

Abstract

In view of the need to enhance the assessment of consumer products called for in the EU Chemicals Strategy for Sustainability, we developed a methodology for evaluating hazard by combining information across different systemic toxicity endpoints and integrating the information with new approach methodologies. This integrates mechanistic information with a view to avoiding redundant in vivo studies, minimising reliance on apical endpoint tests and ultimately devising efficient testing strategies. Here, we present the application of our methodology to carcinogenicity assessment, mapping the available information from toxicity test methods across endpoints to the key characteristics of carcinogens. Test methods are deconstructed to allow the information they provide to be organised in a systematic way, enabling the description of the toxicity mechanisms leading to the adverse outcome. This integrated approach provides a flexible and resource-efficient means of fully exploiting test methods for which test guidelines are available to fulfil regulatory requirements for systemic toxicity assessment as well as identifying where new methods can be integrated.

摘要

鉴于需要加强欧盟化学品可持续性战略中对消费品的评估,我们开发了一种通过结合不同系统毒性终点的信息并将信息与新方法整合来评估危害的方法。这将机制信息与避免重复体内研究、减少对顶极终点测试的依赖并最终设计高效测试策略结合起来。在这里,我们将我们的方法应用于致癌性评估,将来自毒性测试方法的可用信息映射到终点的致癌剂的关键特征。对测试方法进行解构,以便以系统的方式组织它们提供的信息,从而能够描述导致不良后果的毒性机制。这种综合方法为充分利用测试方法提供了一种灵活且资源高效的手段,这些测试方法有测试指南可用于满足系统毒性评估的监管要求,并确定可以整合新方法的地方。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/136d/8166685/3d0c1ac16392/204_2021_3035_Fig1_HTML.jpg

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