Toxicity testing and endocrine disrupting chemicals

内分泌系统 背景(考古学) 内分泌干扰物 第1层网络 不良结局途径 代理(哲学) 测试策略 风险分析(工程) 激素 计算机科学 计算生物学 医学 生物 内科学 互联网 认识论 万维网 哲学 古生物学 程序设计语言 软件
作者
Laura N. Vandenberg
出处
期刊:Advances in pharmacology [Elsevier BV]
卷期号:92: 35-71 被引量:12
标识
DOI:10.1016/bs.apha.2021.05.001
摘要

Abstract Regulatory agencies around the world depend on standardized testing approaches to evaluate environmental chemicals for endocrine disrupting properties. The US Environmental Protection Agency (EPA) has developed a two-tiered testing approach within its Endocrine Disruptor Screening Program (EDSP). The eleven Tier 1 and three Tier 2 EDSP assays can be used to identify chemicals that act as agonists or antagonists of estrogen receptor, androgen receptor, or thyroid hormone receptor, or chemicals that interfere with steroidogenesis. Additional assays have been developed in the context of Tox21, and others have been validated by the OECD. In spite of the availability of validated toxicity tests, problems have been identified with the approaches and methods used to identify endocrine disrupting chemicals (EDCs). This chapter will provide an overview of several of these issues including: (1) The way an EDC is defined by an agency impacts whether a specific test can be used to determine if a chemical is an EDC. This is especially important when considering which assays examine outcomes that are considered “adverse effects.” (2) Some assumptions about the validated studies used to identify EDCs may not be true (e.g., their reproducibility has been questioned). (3) Many of the validated assays are less sensitive than other methods that have not yet been validated. Ultimately, these and other problems contribute to the current landscape, where testing approaches have failed to protect the public from known EDCs. The chapter concludes with a review of approaches that have been taken to improve current guideline studies.
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