| Literature DB >> 28213892 |
Nathan A Berger1, Valerie C Besson2, A Hamid Boulares3, Alexander Bürkle4, Alberto Chiarugi5, Robert S Clark6, Nicola J Curtin7, Salvatore Cuzzocrea8, Ted M Dawson9, Valina L Dawson10, György Haskó11, Lucas Liaudet12, Flavio Moroni13, Pál Pacher14, Peter Radermacher15, Andrew L Salzman16, Solomon H Snyder17, Francisco Garcia Soriano18, Robert P Strosznajder19, Balázs Sümegi20, Raymond A Swanson21, Csaba Szabo22.
Abstract
The recent clinical availability of the PARP inhibitor olaparib (Lynparza) opens the door for potential therapeutic repurposing for non-oncological indications. Considering (a) the preclinical efficacy data with PARP inhibitors in non-oncological diseases and (b) the risk-benefit ratio of treating patients with a compound that inhibits an enzyme that has physiological roles in the regulation of DNA repair, we have selected indications, where (a) the severity of the disease is high, (b) the available therapeutic options are limited, and (c) the duration of PARP inhibitor administration could be short, to provide first-line options for therapeutic repurposing. These indications are as follows: acute ischaemic stroke; traumatic brain injury; septic shock; acute pancreatitis; and severe asthma and severe acute lung injury. In addition, chronic, devastating diseases, where alternative therapeutic options cannot halt disease development (e.g. Parkinson's disease, progressive multiple sclerosis or severe fibrotic diseases), should also be considered. We present a preclinical and clinical action plan for the repurposing of PARP inhibitors. LINKED ARTICLES: This article is part of a themed section on Inventing New Therapies Without Reinventing the Wheel: The Power of Drug Repurposing. To view the other articles in this section visit http://onlinelibrary.wiley.com/doi/10.1111/bph.v175.2/issuetoc.Entities:
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Year: 2017 PMID: 28213892 PMCID: PMC5758399 DOI: 10.1111/bph.13748
Source DB: PubMed Journal: Br J Pharmacol ISSN: 0007-1188 Impact factor: 8.739