Skip to main content

Omics in Toxicology

  • Reference work entry
  • First Online:
Regulatory Toxicology

Abstract

The tremendous progress in the development of new technologies in the areas of molecular biology and bioinformatics enables interrogation of cellular responses to toxicant treatment at a global molecular level, allowing evaluation of toxic effects in the context of molecular pathways.

The major techniques currently employed, especially transcriptomics, but also proteomics and metabolomics, are being used and further evaluated in investigational toxicology. Since they already have been shown to provide increased insight into molecular mechanisms of toxicological effects, regulatory authorities are evaluating such data to prepare themselves for use in regulatory toxicology.

This is a preview of subscription content, log in via an institution to check access.

Access this chapter

Chapter
USD 29.95
Price excludes VAT (USA)
  • Available as PDF
  • Read on any device
  • Instant download
  • Own it forever
eBook
USD 599.99
Price excludes VAT (USA)
  • Available as EPUB and PDF
  • Read on any device
  • Instant download
  • Own it forever
Hardcover Book
USD 549.99
Price excludes VAT (USA)
  • Durable hardcover edition
  • Dispatched in 3 to 5 business days
  • Free shipping worldwide - see info

Tax calculation will be finalised at checkout

Purchases are for personal use only

Institutional subscriptions

References

  • Afshari CA, Hamadeh HK, Bushel PR (2011) The evolution of bioinformatics in toxicology: advancing toxicogenomics. Toxicol Sci 120(Suppl 1):S225–S237

    Article  CAS  PubMed Central  PubMed  Google Scholar 

  • Goodsaid FM, Amur S, Aubrecht J, Burczynski ME, Carl K, Catalano J, Charlab R, Close S, Cornu-Artis C, Essioux L, Fornace AJ Jr, Hinman L, Hong H, Hunt I, Jacobson-Kram D, Jawaid A, Laurie D, Lesko L, Li HH, Lindpaintner K, Mayne J, Morrow P, Papaluca-Amati M, Robison TW, Roth J, Schuppe-Koistinen I, Shi L, Spleiss O, Tong W, Truter SL, Vonderscher J, Westelinck A, Zhang L, Zineh I (2010) Voluntary exploratory data submissions to the US FDA and the EMA: experience and impact. Nat Rev Drug Discov 9:435–445

    Article  CAS  PubMed  Google Scholar 

  • Guo L, Lobenhofer EK, Wang C, Shippy R, Harris SC, Zhang L, Mei N, Chen T, Herman D, Goodsaid FM, Hurban P, Phillips KL, Xu J, Deng X, Sun YA, Tong W, Dragan YP, Shi L (2006) Rat toxicogenomic study reveals analytical consistency across microarray platforms. Nat Biotechnol 24:1162–1169

    Article  CAS  PubMed  Google Scholar 

  • Ly L, Wasinger VC (2011) Protein and peptide fractionation, enrichment and depletion: tools for the complex proteome. Proteomics 11:513–534

    Article  CAS  PubMed  Google Scholar 

  • Woollard PM, Mehta NA, Vamathevan JJ, Van Horn S, Bonde BK, Dow DJ (2011) The application of next-generation sequencing technologies to drug discovery and development. Drug Discov Today 16:512–519

    Article  CAS  PubMed  Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Heidrun Ellinger-Ziegelbauer .

Editor information

Editors and Affiliations

Rights and permissions

Reprints and permissions

Copyright information

© 2014 Springer-Verlag Berlin Heidelberg

About this entry

Cite this entry

Ellinger-Ziegelbauer, H., Ahr, HJ. (2014). Omics in Toxicology. In: Reichl, FX., Schwenk, M. (eds) Regulatory Toxicology. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-642-35374-1_40

Download citation

Publish with us

Policies and ethics