Omic profiling for drug safety assessment: current trends and public-private partnerships

被引:18
作者
Gallagher, William M. [1 ]
Tweats, David [2 ]
Koenig, Jochen [3 ]
机构
[1] Univ Coll Dublin, Conway Inst, Sch Biomol & Biomed Sci, Dublin 2, Ireland
[2] Univ Swansea, Sch Med, Dept Genet, Swansea SA2 8PP, W Glam, Wales
[3] Genedata AG, CH-4016 Basel, Switzerland
关键词
TOXICOGENOMICS; TOXICITY; CARCINOGENICITY; MICROARRAY; SYSTEMS; RAT;
D O I
10.1016/j.drudis.2009.02.001
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The drug development process is currently being hindered by non-optimal prediction of toxicity. Advances in molecular profiling approaches, such as transcriptomics, proteomics and metabolomics, offer the potential to provide it more comprehensive insight into toxicological effects than hitherto possible. These new technologies present their own challenges, however, particularly in relation to standardization and assessment. The focus of this article is on describing the current trends concerning the application of omic approaches in drug safety assessment, with specific emphasis on the role of public-private partnerships in advancing this emerging arena.
引用
收藏
页码:337 / 342
页数:6
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