Drug Repurposing for the Development of Novel Analgesics

被引:37
|
作者
Sisignano, Marco [1 ]
Parnham, Michael J. [2 ]
Geisslinger, Gerd [1 ,2 ]
机构
[1] Goethe Univ Frankfurt, Inst Clin Pharmacol, Pharmazentrum Frankfurt ZAFES, Univ Hosp, D-60590 Frankfurt, Germany
[2] Fraunhofer Inst Mol Biol & Appl Ecol IME, Project Grp Translat Med & Pharmacol TMP, Theodor Stern Kai 7, D-60596 Frankfurt, Germany
关键词
ACTIVATED PROTEIN-KINASE; PAIN CLINICAL-TRIALS; NEUROPATHIC PAIN; PERIPHERAL NEUROPATHY; ION-CHANNEL; PHASE-II; RECEPTOR; SILDENAFIL; MECHANISMS; MINOCYCLINE;
D O I
10.1016/j.tips.2015.11.006
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Drug development consumes huge amounts of time and money and the search for novel analgesics, which are urgently required, is particularly difficult, having resulted in many setbacks in the past. Drug repurposing - the identification of new uses for existing drugs - is an alternative approach, which bypasses most of the time- and cost-consuming components of drug development. Recent, unexpected findings suggest a role for several existing drugs, such as minocycline, ceftriaxone, sivelestat, and pioglitazone, as novel analgesics in chronic and neuropathic pain states. Here, we discuss these findings as well as their proposed antihyperalgesic mechanisms and outline the merits of pathway based repurposing screens, in combination with bioinformatics and novel cellular reprogramming techniques, for the identification of novel analgesics.
引用
收藏
页码:172 / 183
页数:12
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