Systems toxicology: applications of toxicogenomics, transcriptomics, proteomics and metabolomics in toxicology

被引:126
作者
Heijne, Wilbert H. M.
Kienhuis, Anne S.
van Ommen, Ben
Stierum, Rob H. [1 ]
Groten, John P.
机构
[1] DSM Food Specialties R&D, Delft, Netherlands
[2] TNO, Dept Physiol Sci, NL-3700 AJ Zeist, Netherlands
[3] Maastricht Univ, Dept Hlth Risck Anal & Toxicol, Maastricht, Netherlands
[4] Univ Wageningen & Res Ctr, Dept Toxicol, NL-6700 HB Wageningen, Netherlands
关键词
genomics; metabolomics; proteomics; systems biology; toxicogenomics; toxicology; transcriptomics;
D O I
10.1586/14789450.2.5.767
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Toxicogenomics can facilitate the identification and characterization of toxicity, as illustrated in this review. Toxicogenomics, the application of the functional genomics technologies (transcriptomics, proteomics and metabolomics) in toxicology enables the study of adverse effects of xenobiotic substances in relation to structure and activity of the genome. The advantages and limitations of the different technologies are evaluated, and the prospects for integration of the technologies into a systems biology or systems toxicology approach are discussed. Applications of toxicogenomics in various laboratories around the world show that the crucial steps and sequence of events at the molecular level can be studied to provide detailed insights into mechanisms of toxic action. Toxicogenomics allowed for more sensitive and earlier detection of adverse effects in (animal) toxicity studies. Furthermore, the effects of exposure to mixtures could be studied in more detail. This review argues that in the (near) future, human health risk assessment will truly benefit from toxicogenomics (systems toxicology).
引用
收藏
页码:767 / 780
页数:14
相关论文
共 97 条
[61]   Characterization of SDS-PAGE-separated proteins by matrix-assisted laser desorption ionization mass spectrometry [J].
Liang, XL ;
Bai, J ;
Liu, YH ;
Lubman, DM .
ANALYTICAL CHEMISTRY, 1996, 68 (06) :1012-1018
[62]   Genomics, gene expression and DNA arrays [J].
Lockhart, DJ ;
Winzeler, EA .
NATURE, 2000, 405 (6788) :827-836
[63]   Expression monitoring by hybridization to high-density oligonucleotide arrays [J].
Lockhart, DJ ;
Dong, HL ;
Byrne, MC ;
Follettie, MT ;
Gallo, MV ;
Chee, MS ;
Mittmann, M ;
Wang, CW ;
Kobayashi, M ;
Horton, H ;
Brown, EL .
NATURE BIOTECHNOLOGY, 1996, 14 (13) :1675-1680
[64]   Influence of isolation procedure, extracellular matrix and dexamethasone on the regulation of membrane transporters gene expression in rat hepatocytes [J].
Luttringer, O ;
Theil, FP ;
Lavé, T ;
Wernli-Kuratli, K ;
Guentert, TW ;
de Saizieu, A .
BIOCHEMICAL PHARMACOLOGY, 2002, 64 (11) :1637-1650
[65]  
Merchant M, 2000, ELECTROPHORESIS, V21, P1164, DOI 10.1002/(SICI)1522-2683(20000401)21:6<1164::AID-ELPS1164>3.3.CO
[66]  
2-S
[67]  
Merrick BA, 2004, CURR OPIN MOL THER, V6, P600
[68]   'Metabonomics': understanding the metabolic responses of living systems to pathophysiological stimuli via multivariate statistical analysis of biological NMR spectroscopic data [J].
Nicholson, JK ;
Lindon, JC ;
Holmes, E .
XENOBIOTICA, 1999, 29 (11) :1181-1189
[69]  
Nuwaysir EF, 1999, MOL CARCINOGEN, V24, P153, DOI 10.1002/(SICI)1098-2744(199903)24:3<153::AID-MC1>3.0.CO
[70]  
2-P