High-throughput screening of chemical effects on steroidogenesis using H295R human adrenocortical carcinoma cells
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1 resource available
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https://gaftp.epa.gov/COMPTOX/NCCT_Publication_Data/MartinMatt/ToxCast_Steroidogenesis/
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Complete Metadata
| accessLevel | public |
|---|---|
| bureauCode |
[
"020:00"
]
|
| contactPoint |
{
"fn": "Keith Houck",
"hasEmail": "mailto:houck.keith@epa.gov"
}
|
| description | Disruption of steroidogenesis by environmental chemicals can result in altered hormone levels causing adverse reproductive and developmental effects. A high-throughput assay using H295R human adrenocortical carcinoma cells was used to evaluate the effect of 2060 chemical samples on steroidogenesis via high-performance liquid chromatography followed by tandem mass spectrometry quantification of 10 steroid hormones, including progestagens, glucocorticoids, androgens, and estrogens. The study employed a 3 stage screening strategy. The first stage established the maximum tolerated concentration (MTC; ≥ 70% viability) per sample. The second stage quantified changes in hormone levels at the MTC whereas the third stage performed concentration-response (CR) on a subset of samples. At all stages, cells were prestimulated with 10 µM forskolin for 48 h to induce steroidogenesis followed by chemical treatment for 48 h. Of the 2060 chemical samples evaluated, 524 samples were selected for 6-point CR screening, based in part on significantly altering at least 4 hormones at the MTC. CR screening identified 232 chemical samples with concentration-dependent effects on 17β-estradiol and/or testosterone, with 411 chemical samples showing an effect on at least one hormone across the steroidogenesis pathway. Clustering of the concentration-dependent chemical-mediated steroid hormone effects grouped chemical samples into 5 distinct profiles generally representing putative mechanisms of action, including CYP17A1 and HSD3B inhibition. A distinct pattern was observed between imidazole and triazole fungicides suggesting potentially distinct mechanisms of action. From a chemical testing and prioritization perspective, this assay platform provides a robust model for high-throughput screening of chemicals for effects on steroidogenesis. This dataset is associated with the following publication: Karmaus , A., C. Toole, D. Filer , K. Lewis, and M. Martin. (Toxicological Sciences) High-throughput screening of chemical effects on steroidogenesis using H295R human adrenocortical carcinoma cells. TOXICOLOGICAL SCIENCES. Society of Toxicology, 150(2): 323-332, (2016). |
| distribution |
[
{
"title": "https://gaftp.epa.gov/COMPTOX/NCCT_Publication_Data/MartinMatt/ToxCast_Steroidogenesis/",
"accessURL": "https://gaftp.epa.gov/COMPTOX/NCCT_Publication_Data/MartinMatt/ToxCast_Steroidogenesis/"
}
]
|
| identifier | A-x0kx-385 |
| keyword |
[
"ToxCast",
"cancer",
"chemical safety for sustainablity",
"chemical safety research",
"computational toxicology",
"high-throughput toxicology",
"steroidogenesis"
]
|
| license | https://pasteur.epa.gov/license/sciencehub-license.html |
| modified | 2016-04-02 |
| programCode |
[
"020:095"
]
|
| publisher |
{
"name": "U.S. EPA Office of Research and Development (ORD)",
"subOrganizationOf": {
"name": "U.S. Environmental Protection Agency",
"subOrganizationOf": {
"name": "U.S. Government"
}
}
}
|
| references |
[
"https://doi.org/10.1093/toxsci/kfw002"
]
|
| rights |
null
|
| title | High-throughput screening of chemical effects on steroidogenesis using H295R human adrenocortical carcinoma cells |