Doctor Thomas Hartung
Toward a Deeper UnderstandingLeading a revolution in toxicological approachesThomas Hartung, Professor of Evidence-Based Toxicology at Johns Hopkins University, is helping increase the implementation of omics-focused approaches toward a deeper understanding of toxicology. Current toxicological processes and approaches face a variety of challenges and limitations. Methods are often not productive enough or too costly, meaning they cannot be used sustainably, and there is sometimes an over-reliance on animal testing. The current regulations on certain toxicological processes are also highly precautionary; using today's rules, it would be difficult to bring something like aspirin to market, for example. Additionally, the proliferation of new products and treatments from other areas demands new toxicological approaches. Professor Hartung's team sees that the future of toxicological testing as increasingly based on -omics (primarily proteomic, transcriptomic, and metabolic) processes, leading to far more comprehensive toxicological approaches. This work could also help to map out the many ways and processes through which cells can be harmed. Using uniquely powerful Agilent analytical solutions - such as GeneSpring software - data from multiple pathways can be integrated to provide toxicologists with much greater insight into toxicological mechanisms. These results can also enable better assessment and prediction of toxicological endpoints, such as determining whether a particular sample will affect a certain organ. For Research Use Only. Not for use in diagnostic procedures.
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Director, Center for Alternative to Animal Testing (CAAT) |
Selected publications
3S - Systematic, systemic, and systems biology and toxicology.
Metabolomic network analysis of estrogen-stimulated MCF-7 cells: a comparison of overrepresentation analysis, quantitative enrichment analysis and pathway analysis versus metabolite network analysis.
Information-dependent enrichment analysis reveals time-dependent transcriptional regulation of the estrogen pathway of toxicity.
Combination therapy with BPTES nanoparticles and metformin targets the metabolic heterogeneity of pancreatic cancer.
The human toxome project. |