Small-Molecule Inhibitors of PARPs: From Tools for Investigating ADP-Ribosylation to Therapeutics.


Journal

Current topics in microbiology and immunology
ISSN: 0070-217X
Titre abrégé: Curr Top Microbiol Immunol
Pays: Germany
ID NLM: 0110513

Informations de publication

Date de publication:
Historique:
pubmed: 23 9 2018
medline: 14 8 2019
entrez: 23 9 2018
Statut: ppublish

Résumé

Over the last 60 years, poly-ADP-ribose polymerases (PARPs, 17 family members in humans) have emerged as important regulators of physiology and disease. Small-molecule inhibitors have been essential tools for unraveling PARP function, and recently the first PARP inhibitors have been approved for the treatment of various human cancers. However, inhibitors have only been developed for a few PARPs and in vitro profiling has revealed that many of these exhibit polypharmacology across the PARP family. In this review, we discuss the history, development, and current state of the field, highlighting the limitations and opportunities for PARP inhibitor development.

Identifiants

pubmed: 30242511
doi: 10.1007/82_2018_137
doi:

Substances chimiques

Poly(ADP-ribose) Polymerase Inhibitors 0
Poly(ADP-ribose) Polymerases EC 2.4.2.30

Types de publication

Journal Article Review

Langues

eng

Pagination

211-231

Auteurs

Ilsa T Kirby (IT)

Program in Chemical Biology, Oregon Health & Science University, Portland, OR, 97210, USA.
Department of Physiology and Pharmacology, Oregon Health & Science University, Portland, OR, 97210, USA.

Michael S Cohen (MS)

Program in Chemical Biology, Oregon Health & Science University, Portland, OR, 97210, USA. cohenmic@ohsu.edu.
Department of Physiology and Pharmacology, Oregon Health & Science University, Portland, OR, 97210, USA. cohenmic@ohsu.edu.

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Classifications MeSH