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Evaluation of potential sodium-iodide symporter (NIS) inhibitors using a secondary Fischer rat thyroid follicular cell (FRTL-5) radioactive iodide uptake (RAIU) assay.应用次级 Fischer 大鼠甲状腺滤泡细胞(FRTL-5)放射性碘摄取(RAIU)测定法评估潜在的钠碘同向转运体(NIS)抑制剂。
Arch Toxicol. 2020 Mar;94(3):873-885. doi: 10.1007/s00204-020-02664-y. Epub 2020 Feb 17.
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Protein Stability Effects in Aggregate-Based Enzyme Inhibition.基于聚集的酶抑制中蛋白质稳定性的影响。
J Med Chem. 2019 Nov 14;62(21):9593-9599. doi: 10.1021/acs.jmedchem.9b01019. Epub 2019 Oct 17.
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High-throughput screening and chemotype-enrichment analysis of ToxCast phase II chemicals evaluated for human sodium-iodide symporter (NIS) inhibition.高通量筛选和 ToxCast 二期化学物质的化学型富集分析,评估其对人甲状腺钠碘转运体(NIS)的抑制作用。
Environ Int. 2019 May;126:377-386. doi: 10.1016/j.envint.2019.02.024. Epub 2019 Feb 28.
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High-throughput screening and environmental risk assessment: State of the science and emerging applications.高通量筛选与环境风险评估:科学现状与新兴应用。
Environ Toxicol Chem. 2019 Jan;38(1):12-26. doi: 10.1002/etc.4315. Epub 2018 Dec 20.
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Screening the ToxCast Phase 1, Phase 2, and e1k Chemical Libraries for Inhibitors of Iodothyronine Deiodinases.筛选 ToxCast 第 1 阶段、第 2 阶段和 e1k 化学文库中的甲状腺素脱碘酶抑制剂。
Toxicol Sci. 2019 Apr 1;168(2):430-442. doi: 10.1093/toxsci/kfy302.
6
High-Throughput Screening and Quantitative Chemical Ranking for Sodium-Iodide Symporter Inhibitors in ToxCast Phase I Chemical Library.高通量筛选和定量化学排序在 ToxCast 一期化学文库中用于钠碘同向转运体抑制剂。
Environ Sci Technol. 2018 May 1;52(9):5417-5426. doi: 10.1021/acs.est.7b06145. Epub 2018 Apr 11.
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Screening the ToxCast Phase 1 Chemical Library for Inhibition of Deiodinase Type 1 Activity.筛选 ToxCast 阶段 1 化学文库以抑制脱碘酶 1 型活性。
Toxicol Sci. 2018 Apr 1;162(2):570-581. doi: 10.1093/toxsci/kfx279.
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The CompTox Chemistry Dashboard: a community data resource for environmental chemistry.综合毒理化学仪表盘:环境化学的社区数据资源。
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Development of a screening approach to detect thyroid disrupting chemicals that inhibit the human sodium iodide symporter (NIS).开发一种筛选方法以检测抑制人类钠碘同向转运体(NIS)的甲状腺干扰化学物质。
Toxicol In Vitro. 2017 Apr;40:66-78. doi: 10.1016/j.tiv.2016.12.006. Epub 2016 Dec 12.
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tcpl: the ToxCast pipeline for high-throughput screening data.TCPl:用于高通量筛选数据的ToxCast流程
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非洲爪蟾和人类3型碘甲状腺原氨酸脱碘酶对ToxCast化学物质抑制作用的种间敏感性。

Xenopus laevis and human type 3 iodothyronine deiodinase enzyme cross-species sensitivity to inhibition by ToxCast chemicals.

作者信息

Mayasich Sally A, Korte Joseph J, Denny Jeffrey S, Hartig Phillip C, Olker Jennifer H, DeGoey Philip, O'Flanagan Joseph, Degitz Sigmund J, Hornung Michael W

机构信息

Oak Ridge Institute for Science and Education, Oak Ridge, TN, USA; Great Lakes Toxicology and Ecology Division, Center for Computational Toxicology and Ecology, Office of Research and Development, U.S. Environmental Protection Agency, Duluth, MN, USA.

Great Lakes Toxicology and Ecology Division, Center for Computational Toxicology and Ecology, Office of Research and Development, U.S. Environmental Protection Agency, Duluth, MN, USA.

出版信息

Toxicol In Vitro. 2021 Jun;73:105141. doi: 10.1016/j.tiv.2021.105141. Epub 2021 Mar 11.

DOI:10.1016/j.tiv.2021.105141
PMID:33713820
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8167933/
Abstract

Deiodinase enzymes are critical for tissue-specific and temporal control of activation or inactivation of thyroid hormones during vertebrate development, including amphibian metamorphosis. We previously screened ToxCast chemicals for inhibitory activity toward human recombinant Type 3 iodothyronine deiodinase enzyme (hDIO3) and subsequently produced Xenopus laevis recombinant dio3 enzyme (Xldio3) with the goals to identify specific chemical inhibitors of Xldio3, to evaluate cross-species sensitivity and explore whether the human assay results are predictive of the amphibian. We identified a subset of 356 chemicals screened against hDIO3 to test against Xldio3, initially at a single concentration (200 μM), and further tested 79 in concentration-response mode. Most chemicals had IC values lower for hDIO3 than for Xldio3 and many had steep Hill slopes (a potential indication of non-specific inhibition). However, eight of the most potent chemicals are likely specific inhibitors, with IC values of 14 μM or less, Hill slopes near -1 and curves not significantly different between species likely due to conservation of catalytically active amino acids. Controlling for assay conditions, human in vitro screening results can be predictive of activity in the amphibian assay. This study lays the groundwork for future studies using recombinant non-mammalian proteins to test cross-species sensitivity to chemicals. DISCLAIMER: The views expressed in this paper are those of the authors and do not necessarily reflect the views or policies of the U.S. Environmental Protection Agency. Mention of trade names or commercial products does not constitute endorsement or recommendation for use.

摘要

脱碘酶对于脊椎动物发育过程中甲状腺激素激活或失活的组织特异性和时间控制至关重要,包括两栖动物变态发育。我们之前筛选了ToxCast化学物质对人重组3型碘甲状腺原氨酸脱碘酶(hDIO3)的抑制活性,随后制备了非洲爪蟾重组dio3酶(Xldio3),目的是鉴定Xldio3的特异性化学抑制剂,评估跨物种敏感性,并探讨人体试验结果是否能预测两栖动物的情况。我们从针对hDIO3筛选的356种化学物质中挑选出一部分来测试对Xldio3的作用,最初在单一浓度(200 μM)下进行测试,然后对79种进行浓度响应模式测试。大多数化学物质对hDIO3的IC值低于对Xldio3的IC值,且许多具有陡峭的希尔斜率(这可能是非特异性抑制的一个迹象)。然而,八种最有效的化学物质可能是特异性抑制剂,IC值为14 μM或更低,希尔斜率接近 -1,不同物种间曲线无显著差异,这可能是由于催化活性氨基酸保守所致。在控制试验条件的情况下,人体体外筛选结果可预测两栖动物试验中的活性。本研究为未来使用重组非哺乳动物蛋白测试化学物质跨物种敏感性的研究奠定了基础。免责声明:本文所表达的观点仅为作者观点,不一定反映美国环境保护局的观点或政策。提及商品名或商业产品并不构成对其使用的认可或推荐。