Current Chemical Genomics and Translational Medicine




(Discontinued)

ISSN: 2213-9885 ― Volume 12, 2018

Identification of Thyroid Hormone Receptor Active Compounds Using a Quantitative High-Throughput Screening Platform



Jaime Freitas1, 5, Nicole Miller2, Brenda J. Mengeling3, Menghang Xia2, Ruili Huang2, Keith Houck4, Ivonne M.C.M. Rietjens1, J. David Furlow3, *, #, Albertinka J. Murk1, 6, #
1 Division of Toxicology, Wageningen University, Tuinlaan 5, 6703 HE Wageningen, The Netherlands
2 National Center for Advancing Translational Sciences, National Institutes of Health, Bethesda, MD, 20892, USA
3 Department of Neurobiology, Physiology, and Behavior, University of California, Davis 95616, USA
4 National Center for Computational Toxicology, Office of Research and Development, U.S. Environmental Protection Agency, Research Triangle Park, North Carolina 27711, USA
5 Group of Cell Activation and Gene Expression, Institute for Molecular and Cellular Biology, University of Porto, Porto, Portugal
6 Subdepartment of Environmental Technology, Wageningen University, and Wageningen-IMARES, Axis Z (Building number 118), Room TT.1.100, Bornse Weilanden 96708, WG Wageningen, The Netherlands

Abstract

To adapt the use of GH3.TRE-Luc reporter gene cell line for a quantitative high-throughput screening (qHTS) platform, we miniaturized the reporter gene assay to a 1536-well plate format. 1280 chemicals from the Library of Pharmacologically Active Compounds (LOPAC) and the National Toxicology Program (NTP) 1408 compound collection were analyzed to identify potential thyroid hormone receptor (TR) agonists and antagonists. Of the 2688 compounds tested, eight scored as potential TR agonists when the positive hit cut-off was defined at ≥10% efficacy, relative to maximal triiodothyronine (T3) induction, and with only one of those compounds reaching ≥20% efficacy. One common class of compounds positive in the agonist assays were retinoids such as all-trans retinoic acid, which are likely acting via the retinoid-X receptor, the heterodimer partner with the TR. Five potential TR antagonists were identified, including the antiallergy drug tranilast and the anxiolytic drug SB 205384 but also some cytotoxic compounds like 5-fluorouracil. None of the inactive compounds were structurally related to T3, nor had been reported elsewhere to be thyroid hormone disruptors, so false negatives were not detected. None of the low potency (>100µM) TR agonists resembled T3 or T4, thus these may not bind directly in the ligand-binding pocket of the receptor. For TR agonists, in the qHTS, a hit cut-off of ≥20% efficacy at 100 µM may avoid identification of positives with low or no physiological relevance. The miniaturized GH3.TRE-Luc assay offers a promising addition to the in vitro test battery for endocrine disruption, and given the low percentage of compounds testing positive, its high-throughput nature is an important advantage for future toxicological screening.

Keywords : Endocrine disruption, pituitary cells, quantitative high-throughput screening, thyroid hormone receptor, reporter gene assay, retinoid-X receptor.


Article Information


Identifiers and Pagination:

Year: 2014
Volume: 8
First Page: 36
Last Page: 46
Publisher Id: CCGTM-8-36
DOI: 10.2174/2213988501408010036

Article History:

Received Date: 2/11/2013
Revision Received Date: 9/12/2013
Acceptance Date: 12/12/2013
Electronic publication date: 7/3/2014
Collection year: 2014

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© Freitas et al.; Licensee Bentham Open.

open-access license: This is an open access article licensed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted, non-commercial use, distribution and reproduction in any medium, provided the work is properly cited.


* Address correspondence to this author at the Department of Neurobiology, Physiology, and Behavior, University of California, Davis, CA 95616; Tel: (530)754-8609; Fax: (530) 752-5582. E-mail: jdfurlow@ucdavis.edu# Both authors contributes equally.



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