The ChemScreen project to design a pragmatic alternative approach to predict reproductive toxicity of chemicals

被引:23
作者
van der Burg, Bart [1 ]
Wedebye, Eva Bay [2 ]
Dietrich, Daniel R. [3 ]
Jaworska, Joanna [4 ]
Mangelsdorf, Inge [5 ]
Paune, Eduard [6 ]
Schwarz, Michael [7 ]
Piersma, Aldert H. [8 ,9 ]
Kroese, E. Dinant [10 ]
机构
[1] BioDetect Syst BV, Amsterdam, Netherlands
[2] Danish Tech Univ, Lyngby, Denmark
[3] Univ Konstanz, Constance, Germany
[4] Procter & Gamble Co, Brussels, Belgium
[5] Fraunhofer ITEM, Hannover, Germany
[6] Simpple, Tarragona, Spain
[7] Univ Tubingen, Tubingen, Germany
[8] Natl Inst Publ Hlth & Environm, NL-3720 BA Bilthoven, Netherlands
[9] Univ Utrecht, Utrecht, Netherlands
[10] TNO, NL-3700 AJ Zeist, Netherlands
关键词
In vitro; In silico; Integrated testing; Read accross; Reproductive toxicity; Endocrine disruption; STEM-CELL TEST; IN-VITRO; DEVELOPMENTAL TOXICITY; STRUCTURAL FEATURES; ESTROGEN-RECEPTORS; CALUX METHOD; TEST BATTERY; VIVO; MODELS; PREVALIDATION;
D O I
10.1016/j.reprotox.2015.01.008
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
There is a great need for rapid testing strategies for reproductive toxicity testing, avoiding animal use. The EU Framework program 7 project ChemScreen aimed to fill this gap in a pragmatic manner preferably using validated existing tools and place them in an innovative alternative testing strategy. In our approach we combined knowledge on critical processes affected by reproductive toxicants with knowledge on the mechanistic basis of such effects. We used in silico methods for prescreening chemicals for relevant toxic effects aiming at reduced testing needs. For those chemicals that need testing we have set up an in vitro screening panel that includes mechanistic high throughput methods and lower throughput assays that measure more integrative endpoints. In silico pharmacokinetic modules were developed for rapid exposure predictions via diverse exposure routes. These modules to match in vitro and in vivo exposure levels greatly improved predictivity of the in vitro tests. As a further step, we have generated examples how to predict reproductive toxicity of chemicals using available data. We have executed formal validations of panel constituents and also used more innovative manners to validate the test panel using mechanistic approaches. We are actively engaged in promoting regulatory acceptance of the tools developed as an essential step towards practical application, including case studies for read-across purposes. With this approach, a significant saving in animal use and associated costs seemi very feasible. (C) 2015 Elsevier Inc. All rights reserved.
引用
收藏
页码:114 / 123
页数:10
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