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Identifying and categorizing compounds that reduce corneal transforming growth factor beta induced protein levels: a scoping review.
- Source :
-
Expert review of clinical pharmacology [Expert Rev Clin Pharmacol] 2022 Dec; Vol. 15 (12), pp. 1423-1442. Date of Electronic Publication: 2022 Nov 10. - Publication Year :
- 2022
-
Abstract
- Introduction: Transforming growth factor beta induced ( TGFBI ) gene mutations have been reported as the cause of a group of genetically inherited, visually debilitating, corneal dystrophies (CD). A scoping literature review to identify and categorize compounds that inhibit corneal TGFBI expression and/or promote TGFBIp degradation was performed. Emphasis was given to their potential to be used as a cost-effective approach via drug repurposing.<br />Areas Covered: We performed a thorough search of original peer-reviewed literature using electronic bibliographic databases and selected articles according to a set of criteria. The total number of articles retrieved from the search terms applied to the databases was 2344. The number of relevant full-text articles included added up to 19. We identified 16 compounds that can theoretically reduce the levels of mutant TGFBIp in human corneal cells.<br />Expert Opinion: Currently, the only temporary treatments available for this condition are lubricant drops and surgery. Here, we explored the crosstalk between cascades that regulate TGFBI expression and identified compounds that target these pathways. Compounds that inhibit DNA synthesis and function, increase elimination of TGFBIp or bind to mutant TGFBIp were also explored with the aim of highlighting promising compounds that can be used in future cost-effective drug-repurposing studies.
- Subjects :
- Humans
Extracellular Matrix Proteins genetics
Extracellular Matrix Proteins metabolism
Cornea metabolism
Mutation
Transforming Growth Factor beta genetics
Transforming Growth Factor beta metabolism
Corneal Dystrophies, Hereditary genetics
Corneal Dystrophies, Hereditary metabolism
Corneal Dystrophies, Hereditary therapy
Subjects
Details
- Language :
- English
- ISSN :
- 1751-2441
- Volume :
- 15
- Issue :
- 12
- Database :
- MEDLINE
- Journal :
- Expert review of clinical pharmacology
- Publication Type :
- Academic Journal
- Accession number :
- 36308770
- Full Text :
- https://doi.org/10.1080/17512433.2022.2142560