Literature DB >> 15331182

Interaction networks: coordinating responses to xenobiotic exposure.

Nick Plant1.   

Abstract

In the last decade the increased usage of '-omic' technologies, plus the sequencing of over 800 complete genomes has led to a vast increase in the amount of information available to the researcher for examining cellular responses to xenobiotics. Much effort has been put into the identification and analysis of expression profiles associated with pathobiological conditions and/or xenobiotic exposure. These profiles are commonly used in two applications. Firstly, comparative profile experiments are used to classify pathobiological states and for the screening of novel chemical entities to predict their action(s) on the body. Secondly, mechanistic investigations will gain information on the molecular mechanisms underlying toxic responses/pathobiological states. During the course of such analysis it has become increasingly clear that a series of highly refined interaction networks exist within the body, regulating both the sensitivity and selectivity of the body's response to pathobiological states/xenobiotic exposure. These interaction networks exist at several levels: Firstly, within individual cells, the interaction between factors that transmit xenobiotics signals will determine the overall cellular response. Secondly, intraorgan communication occurs between the different cell types/sub-types which makes up an organ, coordinating the overall organ response. Finally, interorgan interactions provide axes of response through the body.

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Year:  2004        PMID: 15331182     DOI: 10.1016/j.tox.2004.06.028

Source DB:  PubMed          Journal:  Toxicology        ISSN: 0300-483X            Impact factor:   4.221


  2 in total

1.  In silico and in vitro modeling of hepatocyte drug transport processes: importance of ABCC2 expression levels in the disposition of carboxydichlorofluroscein.

Authors:  Katharine Howe; G Gordon Gibson; Tanya Coleman; Nick Plant
Journal:  Drug Metab Dispos       Date:  2008-11-20       Impact factor: 3.922

2.  A PXR-mediated negative feedback loop attenuates the expression of CYP3A in response to the PXR agonist pregnenalone-16α-carbonitrile.

Authors:  Ian Bailey; G Gordon Gibson; Kathryn Plant; Mark Graham; Nick Plant
Journal:  PLoS One       Date:  2011-02-02       Impact factor: 3.240

  2 in total

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