| Literature DB >> 25527862 |
Bart van der Burg1, Bart Pieterse2, Harrie Buist3, Geertje Lewin4, Sander C van der Linden2, Hai-yen Man2, Emiel Rorije5, Aldert H Piersma5, Inge Mangelsdorf4, Andre P M Wolterbeek3, E Dinant Kroese3, Barbara van Vugt-Lussenburg2.
Abstract
There is a great need for alternative testing methods for reproductive toxicants that are practical, fast, cost-effective and easy to interpret. Previously we followed a pragmatic approach using readily available tests, which was successful in predicting reproductive toxicity of chemicals [13]. This initial battery still contained apical tests and is fairly complex and low in its throughput. The current study aimed to simplify this screening battery using a mechanistic approach and a panel of high throughput CALUX reporter gene assays. A mechanistic approach was taken to validate this high throughput test battery. To this end it was challenged with two preselected sets of chemicals addressing two major apical effect classes relevant in reproductive toxicity. We found selectivity in this battery in that 82% of the compounds inducing reproductive organ deformities were predicted correctly, while for compounds inducing neural tube defects this was the case in 47% only. This is consistent with the mechanisms of toxicity covered in the battery. The most informative assays in the battery were ERalpha CALUX to measure estrogenicity and the AR-anti CALUX assay to measure androgen receptor antagonism.Entities:
Keywords: Estrogen–androgen reporter gene assay; High throughput screening; Mechanistic validation; Reproductive organ deformities
Mesh:
Substances:
Year: 2014 PMID: 25527862 DOI: 10.1016/j.reprotox.2014.11.011
Source DB: PubMed Journal: Reprod Toxicol ISSN: 0890-6238 Impact factor: 3.143