Drug-induced nephrotoxicity is a major cause of kidney dysfunction with potentially fatal consequences and can hamper the research and development of new pharmaceuticals. This emphasises the need for new methods for earlier and more accurate diagnosis to avoid drug-induced kidney injury. Here, we present a systematic review of the available approaches to study drug-induced kidney injury, as one of the most common reasons for drug withdrawal, in vitro. The systematic review approach was selected to ensure that our findings are as objective and reproducible as possible. A novel study quality checklist, named validation score, was developed based on published regulatory guidance and industrial perspectives, and models returned by the search strategy were analysed as per their overall complexity and the kidney region studied. Our search strategy returned 1731 articles supplemented by 337 from secondary sources, of which 57 articles met the inclusion criteria for final analysis. Our results show that the proximal tubule dominates the field (84%), followed by the glomerulus and Bowman's capsule (7%). Of all drugs investigated, the focus was most on cisplatin (n = 29, 50.1% of final inclusions). We found that with increasing model complexity the validation score increased, reflecting the value of innovative in vitro models. Furthermore, although the highly diverse usage of cell lines and modelling approaches prevented a strong statistical verification through a meta-analysis, our findings show the downstream potential of such approaches in personalised medicine and for rare diseases where traditional trials are not feasible.
机构:
Millennium Pharmaceut Inc, Dept Drug Metab & Pharmacokinet, Cambridge, MA 02139 USAMillennium Pharmaceut Inc, Dept Drug Metab & Pharmacokinet, Cambridge, MA 02139 USA
机构:
Dalian Univ Technol, Dept Chem Engn, State Key Lab Fine Chem, Dalian, Peoples R China
Dalian Univ Technol, Sch Pharmaceut Sci & Technol, Dalian, Peoples R ChinaDalian Univ Technol, Dept Chem Engn, State Key Lab Fine Chem, Dalian, Peoples R China
Qu, Yueyang
An, Fan
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机构:
Dalian Med Univ, Inst Canc Stem Cell, Dalian, Peoples R ChinaDalian Univ Technol, Dept Chem Engn, State Key Lab Fine Chem, Dalian, Peoples R China
An, Fan
Luo, Yong
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机构:
Dalian Univ Technol, Dept Chem Engn, State Key Lab Fine Chem, Dalian, Peoples R China
Dalian Univ Technol, Sch Pharmaceut Sci & Technol, Dalian, Peoples R ChinaDalian Univ Technol, Dept Chem Engn, State Key Lab Fine Chem, Dalian, Peoples R China
Luo, Yong
Lu, Yao
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机构:
Chinese Acad Sci, Dalian Inst Chem Phys, Dalian, Peoples R ChinaDalian Univ Technol, Dept Chem Engn, State Key Lab Fine Chem, Dalian, Peoples R China
Lu, Yao
Liu, Tingjiao
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Dalian Med Univ, Coll Stomatol, Dalian, Peoples R ChinaDalian Univ Technol, Dept Chem Engn, State Key Lab Fine Chem, Dalian, Peoples R China
Liu, Tingjiao
Zhao, Weijie
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机构:
Dalian Univ Technol, Dept Chem Engn, State Key Lab Fine Chem, Dalian, Peoples R China
Dalian Univ Technol, Sch Pharmaceut Sci & Technol, Dalian, Peoples R ChinaDalian Univ Technol, Dept Chem Engn, State Key Lab Fine Chem, Dalian, Peoples R China
Zhao, Weijie
Lin, Bingcheng
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h-index: 0
机构:
Dalian Univ Technol, Dept Chem Engn, State Key Lab Fine Chem, Dalian, Peoples R China
Dalian Univ Technol, Sch Pharmaceut Sci & Technol, Dalian, Peoples R ChinaDalian Univ Technol, Dept Chem Engn, State Key Lab Fine Chem, Dalian, Peoples R China
机构:
Pfizer Worldwide Res Dev & Med, Drug Safety R&D, One Portland St, Cambridge, MA 02139 USAPfizer Worldwide Res Dev & Med, Drug Safety R&D, One Portland St, Cambridge, MA 02139 USA