Toward predictive models for drug-induced liver injury in humans: are we there yet?

被引:98
作者
Chen, Minjun [1 ]
Bisgin, Halil [1 ]
Tong, Lillian [1 ,2 ]
Hong, Huixiao [1 ]
Fang, Hong [3 ]
Borlak, Juergen [4 ]
Tong, Weida [1 ]
机构
[1] US FDA, Natl Ctr Toxicol Res, Div Bioinformat & Biostat, Jefferson, AR 72079 USA
[2] CALTECH, Div Biol & Biol Engn, Pasadena, CA 91125 USA
[3] US FDA, Natl Ctr Toxicol Res, Off Sci Coordinat, Jefferson, AR 72079 USA
[4] Hannover Med Sch, Ctr Pharmacol & Toxicol, Hannover, Germany
关键词
biomarker; drug label; drug safety; drug-induced liver injury; predictive model; IN-SILICO MODELS; HUMAN HEPATOTOXICITY; HUMAN PHARMACOKINETICS; TOXICITY; ASSAY; QSAR; TOXICOGENOMICS; CLASSIFICATION; DISCOVERY; SAFETY;
D O I
10.2217/bmm.13.146
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Drug-induced liver injury (DILI) is a frequent cause for the termination of drug development programs and a leading reason of drug withdrawal from the marketplace. Unfortunately, the current preclinical testing strategies, including the regulatory-required animal toxicity studies or simple in vitro tests, are insufficiently powered to predict DILI in patients reliably. Notably, the limited predictive power of such testing strategies is mostly attributed to the complex nature of DILI, a poor understanding of its mechanism, a scarcity of human hepatotoxicity data and inadequate bioinformatics capabilities. With the advent of high-content screening assays, toxicogenomics and bioinformatics, multiple end points can be studied simultaneously to improve prediction of clinically relevant DILIs. This review focuses on the current state of efforts in developing predictive models from diverse data sources for potential use in detecting human hepatotoxicity, and also aims to provide perspectives on how to further improve DILI prediction.
引用
收藏
页码:201 / 213
页数:13
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