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Inhibitors of DNA Glycosylases as Prospective Drugs.
- Source :
-
International journal of molecular sciences [Int J Mol Sci] 2020 Apr 28; Vol. 21 (9). Date of Electronic Publication: 2020 Apr 28. - Publication Year :
- 2020
-
Abstract
- DNA glycosylases are enzymes that initiate the base excision repair pathway, a major biochemical process that protects the genomes of all living organisms from intrinsically and environmentally inflicted damage. Recently, base excision repair inhibition proved to be a viable strategy for the therapy of tumors that have lost alternative repair pathways, such as BRCA-deficient cancers sensitive to poly(ADP-ribose)polymerase inhibition. However, drugs targeting DNA glycosylases are still in development and so far have not advanced to clinical trials. In this review, we cover the attempts to validate DNA glycosylases as suitable targets for inhibition in the pharmacological treatment of cancer, neurodegenerative diseases, chronic inflammation, bacterial and viral infections. We discuss the glycosylase inhibitors described so far and survey the advances in the assays for DNA glycosylase reactions that may be used to screen pharmacological libraries for new active compounds.<br />Competing Interests: The authors declare no conflict of interest. The funders had no role in the design of the study; in the collection, analyses, or interpretation of data; in the writing of the manuscript, or in the decision to publish the results.
- Subjects :
- Bacterial Infections drug therapy
Bacterial Infections enzymology
DNA Repair
Drug Discovery
Enzyme Inhibitors therapeutic use
Humans
Inflammation drug therapy
Inflammation enzymology
Neoplasms drug therapy
Neoplasms enzymology
Neurodegenerative Diseases drug therapy
Neurodegenerative Diseases enzymology
Small Molecule Libraries therapeutic use
Virus Diseases drug therapy
Virus Diseases enzymology
DNA Glycosylases antagonists & inhibitors
Enzyme Inhibitors pharmacology
Small Molecule Libraries pharmacology
Subjects
Details
- Language :
- English
- ISSN :
- 1422-0067
- Volume :
- 21
- Issue :
- 9
- Database :
- MEDLINE
- Journal :
- International journal of molecular sciences
- Publication Type :
- Academic Journal
- Accession number :
- 32354123
- Full Text :
- https://doi.org/10.3390/ijms21093118