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Intra-laboratory validated human cell-based in vitro vasculogenesis/angiogenesis test with serum-free medium
•Vasculogenesis/angiogenesis test intra-laboratory validated (OECD GD34).•Vasculogenesis/angiogenesis test is found to be reproducible and repeatable.•Test suitable for predicting inhibition of vascular formation and teratogenesis. Vasculogenesis and angiogenesis are the processes by which new blood...
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Published in: | Reproductive toxicology (Elmsford, N.Y.) N.Y.), 2017-06, Vol.70, p.116-125 |
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Main Authors: | , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | •Vasculogenesis/angiogenesis test intra-laboratory validated (OECD GD34).•Vasculogenesis/angiogenesis test is found to be reproducible and repeatable.•Test suitable for predicting inhibition of vascular formation and teratogenesis.
Vasculogenesis and angiogenesis are the processes by which new blood vessels are formed. We have developed a serum-free human adipose stromal cell and umbilical cord vein endothelial cell based vasculogenesis/angiogenesis test. In this study, the test was validated in our GLP laboratory following the OECD Guidance Document 34 [1] using erlotinib, acetylic salicylic acid, levamisole, 2-methoxyestradiol, anti‐VEGF, methimazole, and D-mannitol to show its reproducibility, repeatability, and predictivity for humans. The results were obtained from immunostained tubule structures and cytotoxicity assessment.
The performance of the test was evaluated using 26 suspected teratogens and non-teratogens. The positive predictive value was 71.4% and the negative predictive value was 50.0%, indicating that inhibition of vasculogenesis is a significant mechanism behind teratogenesis. In conclusion, this test has great potential to be a screening test for prioritization purposes of chemicals and to be a test in a battery to predict developmental hazards in a regulatory context. |
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ISSN: | 0890-6238 1873-1708 |
DOI: | 10.1016/j.reprotox.2016.11.015 |