共 100 条
Use of transcriptomics in understanding mechanisms of drug-induced toxicity
被引:30
作者:

Cui, Yuxia
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h-index: 0
机构:
NIEHS, Environm Stress & Canc Grp, Res Triangle Pk, NC 27709 USA NIEHS, Environm Stress & Canc Grp, Res Triangle Pk, NC 27709 USA

Paules, Richard S.
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h-index: 0
机构:
NIEHS, Environm Stress & Canc Grp, Res Triangle Pk, NC 27709 USA NIEHS, Environm Stress & Canc Grp, Res Triangle Pk, NC 27709 USA
机构:
[1] NIEHS, Environm Stress & Canc Grp, Res Triangle Pk, NC 27709 USA
关键词:
adverse drug reaction;
hepatotoxicity;
idiosyncratic toxicity;
mechanism;
nephrotoxicity;
toxicogenomics;
GENE-EXPRESSION ANALYSIS;
INDUCED LIVER-INJURY;
ACETAMINOPHEN-INDUCED HEPATOTOXICITY;
METHAPYRILENE-INDUCED HEPATOTOXICITY;
PERIPHERAL-BLOOD TRANSCRIPTOME;
PRIMARY HUMAN HEPATOCYTES;
RENAL TUBULAR TOXICITY;
IN-VITRO;
PPAR-ALPHA;
MICROARRAY ANALYSIS;
D O I:
10.2217/PGS.10.37
中图分类号:
R9 [药学];
学科分类号:
1007 ;
摘要:
Adverse drug reactions (ADRs) are an important clinical issue and a serious public health risk. Understanding the underlying mechanisms is critical for clinical diagnosis and management of different ADRs. Toxicogenomics can reveal impacts on biological pathways and processes that had not previously been considered to be involved in a drug response. Mechanistic hypotheses can be generated that can then be experimentally tested using the full arsenal of pharmacology, toxicology, molecular biology and genetics. Recent transcriptomic studies on drug-induced toxicity, which have provided valuable mechanistic insights into various ADRs, have been reviewed with a focus on nephrotoxicity and hepatotoxicity. Related issues have been discussed, including extrapolation of mechanistic findings from experimental model systems to humans using blood as a surrogate tissue for organ damage and comparative systems biology approaches.
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收藏
页码:573 / 585
页数:13
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