An exposure:activity profiling method for interpreting high-throughput screening data for estrogenic activity-Proof of concept

被引:43
作者
Becker, Richard A. [1 ]
Friedman, Katie Paul [2 ]
Simon, Ted W. [3 ]
Marty, M. Sue [4 ]
Patlewicz, Grace [5 ]
Rowlands, J. Craig [4 ]
机构
[1] Amer Chem Council, Washington, DC 20002 USA
[2] Bayer CropSci LP, Res Triangle Pk, NC USA
[3] Ted Simon LLC, Winston, GA USA
[4] Dow Chem Co USA, Midland, MI 48674 USA
[5] DuPont Haskell Global Ctr Hlth & Environm Sci, Newark, DE USA
关键词
Endocrine disruption; Estrogen assays; Exposure:activity ratio; Relative estrogenic exposure:activity quotient; Genistein; ToxCast (TM); Tox21; Exposure; Potency; ENDOCRINE-DISRUPTING CHEMICALS; ACTIVATION ASSAY T47D-KBLUC; EQUIVALENTS EXPERT WORKSHOP; COREGULATOR BINDING ASSAY; BREAST-CANCER RISK; IN-VIVO HAZARD; BISPHENOL-A; POSTMENOPAUSAL WOMEN; SOY ISOFLAVONES; DOSE-RESPONSE;
D O I
10.1016/j.yrtph.2015.01.008
中图分类号
DF [法律]; D9 [法律]; R [医药、卫生];
学科分类号
0301 ; 10 ;
摘要
Rapid high throughput in vitro screening (HTS) assays are now available for characterizing dose-responses in assays that have been selected for their sensitivity in detecting estrogen-related endpoints. For example, EPA's ToxCast (TM) program recently released endocrine assay results for more than 1800 substances and the interagency Tox21 consortium is in the process of releasing data for approximately 10,000 chemicals. But such activity measurements alone fall short for the purposes of priority setting or screening because the relevant exposure context is not considered. Here, we extend the method of exposure:activity profiling by calculating the exposure:activity ratios (EARs) using human exposure estimates and AC50 values for a range of chemicals tested in a suite of seven estrogenic assays in ToxCast (TM) and Tox21. To provide additional context, relative estrogenic exposure:activity quotients (REEAQ) were derived by comparing chemical-specific EARS to the EAR of the ubiquitous dietary phytoestrogen, genistein (GEN). Although the activity of a substance in HIS-endocrine assays is not a measure of health hazard or risk, understanding how such a dose compares to human exposures provides a valuable additional metric that can be used in decision-making; substances with small EARs and REEAQs would indicate low priority for further endocrine screening or testing. (C) 2015 The Authors. Published by Elsevier Inc.
引用
收藏
页码:398 / 408
页数:11
相关论文
共 85 条
[31]   In Vitro and Modelling Approaches to Risk Assessment from the US Environmental Protection Agency ToxCast Programme [J].
Judson, Richard ;
Houck, Keith ;
Martin, Matt ;
Knudsen, Thomas ;
Thomas, Russell S. ;
Sipes, Nisha ;
Shah, Imran ;
Wambaugh, John ;
Crofton, Kevin .
BASIC & CLINICAL PHARMACOLOGY & TOXICOLOGY, 2014, 115 (01) :69-76
[32]   Estimating Toxicity-Related Biological Pathway Altering Doses for High-Throughput Chemical Risk Assessment [J].
Judson, Richard S. ;
Kavlock, Robert J. ;
Setzer, R. Woodrow ;
Hubal, Elaine A. Cohen ;
Martin, Matthew T. ;
Knudsen, Thomas B. ;
Houck, Keith A. ;
Thomas, Russell S. ;
Wetmore, Barbara A. ;
Dix, David J. .
CHEMICAL RESEARCH IN TOXICOLOGY, 2011, 24 (04) :451-462
[33]   In Vitro Screening of Environmental Chemicals for Targeted Testing Prioritization: The ToxCast Project [J].
Judson, Richard S. ;
Houck, Keith A. ;
Kavlock, Robert J. ;
Knudsen, Thomas B. ;
Martin, Matthew T. ;
Mortensen, Holly M. ;
Reif, David M. ;
Rotroff, Daniel M. ;
Shah, Imran ;
Richard, Ann M. ;
Dix, David J. .
ENVIRONMENTAL HEALTH PERSPECTIVES, 2010, 118 (04) :485-492
[34]  
KRAUS WL, 1995, MOL CELL BIOL, V15, P1847
[35]   Guidelines for the communication of Biomonitoring Equivalents: Report from the Biomonitoring Equivalents Expert Workshop [J].
LaKind, Judy S. ;
Aylward, Lesa L. ;
Brunk, Conrad ;
DiZio, Stephen ;
Dourson, Michael ;
Goldstein, Daniel A. ;
Kilpatrick, Michael E. ;
Krewski, Daniel ;
Bartels, Michael J. ;
Barton, Hugh A. ;
Boogaard, Peter J. ;
Lipscomb, John ;
Krishnan, Kannan ;
Nordberg, Monica ;
Okino, Miles ;
Tan, Yu-Mei ;
Viau, Claude ;
Yager, Janice W. ;
Hays, Sean M. .
REGULATORY TOXICOLOGY AND PHARMACOLOGY, 2008, 51 (03) :S16-S26
[36]   Plant-derived 3,3′-diindolylmethane is a strong androgen antagonist in human prostate cancer cells [J].
Le, HT ;
Schaldach, CM ;
Firestone, GL ;
Bjeldanes, LF .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2003, 278 (23) :21136-21145
[37]   Luteinizing hormone receptor (lhcgr) as a marker gene for characterizing estrogenic endocrine-disrupting chemicals in zebrafish ovarian follicle cells [J].
Liu, Ka-Cheuk ;
Wu, Rudolf S. S. ;
Ge, Wei .
GENERAL AND COMPARATIVE ENDOCRINOLOGY, 2013, 192 :89-94
[38]  
Metzner JE, 2009, ARZNEIMITTELFORSCH, V59, P513
[39]   A Multifactorial Approach to Hepatobiliary Transporter Assessment Enables Improved Therapeutic Compound Development [J].
Morgan, Ryan E. ;
van Staden, Carlo J. ;
Chen, Yuan ;
Kalyanaraman, Natarajan ;
Kalanzi, Jackson ;
Dunn, Robert T., II ;
Afshari, Cynthia A. ;
Hamadeh, Hisham K. .
TOXICOLOGICAL SCIENCES, 2013, 136 (01) :216-241
[40]   Mechanism-based testing strategy using in vitro approaches for identification of thyroid hormone disrupting chemicals [J].
Murk, AlberTinka J. ;
Rijntjes, Eddy ;
Blaauboer, Bas J. ;
Clewell, Rebecca ;
Crofton, Kevin M. ;
Dingemans, Milou M. L. ;
Furlow, J. David ;
Kavlock, Robert ;
Koehrle, Josef ;
Opitz, Robert ;
Traas, Theo ;
Visser, Theo J. ;
Xia, Menghang ;
Gutleb, Arno C. .
TOXICOLOGY IN VITRO, 2013, 27 (04) :1320-1346