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Grouping 34 Chemicals Based on Mode of Action Using Connectivity Mapping.
- Source :
-
Toxicological sciences : an official journal of the Society of Toxicology [Toxicol Sci] 2016 Jun; Vol. 151 (2), pp. 447-61. Date of Electronic Publication: 2016 Mar 29. - Publication Year :
- 2016
-
Abstract
- Connectivity mapping is a method used in the pharmaceutical industry to find connections between small molecules, disease states, and genes. The concept can be applied to a predictive toxicology paradigm to find connections between chemicals, adverse events, and genes. In order to assess the applicability of the technique for predictive toxicology purposes, we performed gene array experiments on 34 different chemicals: bisphenol A, genistein, ethinyl-estradiol, tamoxifen, clofibrate, dehydorepiandrosterone, troglitazone, diethylhexyl phthalate, flutamide, trenbolone, phenobarbital, retinoic acid, thyroxine, 1α,25-dihydroxyvitamin D3, clobetasol, farnesol, chenodeoxycholic acid, progesterone, RU486, ketoconazole, valproic acid, desferrioxamine, amoxicillin, 6-aminonicotinamide, metformin, phenformin, methotrexate, vinblastine, ANIT (1-naphthyl isothiocyanate), griseofulvin, nicotine, imidacloprid, vorinostat, 2,3,7,8-tetrachloro-dibenzo-p-dioxin (TCDD) at the 6-, 24-, and 48-hour time points for 3 different concentrations in the 4 cell lines: MCF7, Ishikawa, HepaRG, and HepG2 GEO (super series accession no.: GSE69851). The 34 chemicals were grouped in to predefined mode of action (MOA)-based chemical classes based on current literature. Connectivity mapping was used to find linkages between each chemical and between chemical classes. Cell line-specific linkages were compared with each other and to test whether the method was platform and user independent, a similar analysis was performed against publicly available data. The study showed that the method can group chemicals based on MOAs and the inter-chemical class comparison alluded to connections between MOAs that were not predefined. Comparison to the publicly available data showed that the method is user and platform independent. The results provide an example of an alternate data analysis process for high-content data, beneficial for predictive toxicology, especially when grouping chemicals for read across purposes.<br /> (© The Author 2016. Published by Oxford University Press on behalf of the Society of Toxicology. All rights reserved. For Permissions, please e-mail: journals.permissions@oup.com.)
- Subjects :
- Databases, Genetic
Dose-Response Relationship, Drug
Gene Expression Profiling methods
Gene Expression Regulation, Neoplastic drug effects
Hep G2 Cells
Humans
MCF-7 Cells
Molecular Structure
Oligonucleotide Array Sequence Analysis
Pharmaceutical Preparations chemistry
Structure-Activity Relationship
Time Factors
Transcriptome drug effects
Computational Biology
Pharmaceutical Preparations classification
Subjects
Details
- Language :
- English
- ISSN :
- 1096-0929
- Volume :
- 151
- Issue :
- 2
- Database :
- MEDLINE
- Journal :
- Toxicological sciences : an official journal of the Society of Toxicology
- Publication Type :
- Academic Journal
- Accession number :
- 27026708
- Full Text :
- https://doi.org/10.1093/toxsci/kfw058