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

Author:

Chen Minjun1,Bisgin Halil1,Tong Lillian12,Hong Huixiao1,Fang Hong3,Borlak Jürgen4,Tong Weida5

Affiliation:

1. Division of Bioinformatics & Biostatistics, National Center for Toxicological Research, The US Food & Drug Administration, Jefferson, AR, USA

2. Division of Biology & Biological Engineering, California Institute of Technology, Pasadena, CA, USA

3. Office of Scientific Coordination, National Center for Toxicological Research, The US Food & Drug Administration, Jefferson, AR, USA

4. Center of Pharmacology & Toxicology, Hannover Medical School, Hannover, Germany

5. Division of Bioinformatics & Biostatistics, National Center for Toxicological Research, The US Food & Drug Administration, Jefferson, AR, USA.

Abstract

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.

Publisher

Future Medicine Ltd

Subject

Biochemistry (medical),Clinical Biochemistry,Drug Discovery

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