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DYRK1A Inhibitors as Potential Therapeutics for β-Cell Regeneration for Diabetes.
- Source :
-
Journal of medicinal chemistry [J Med Chem] 2021 Mar 25; Vol. 64 (6), pp. 2901-2922. Date of Electronic Publication: 2021 Mar 08. - Publication Year :
- 2021
-
Abstract
- According to the World Health Organization (WHO), 422 million people are suffering from diabetes worldwide. Current diabetes therapies are focused on optimizing blood glucose control to prevent long-term diabetes complications. Unfortunately, current therapies have failed to achieve glycemic targets in the majority of people with diabetes. In this context, regeneration of functional insulin-producing human β-cells in people with diabetes through the use of DYRK1A inhibitor drugs has recently received special attention. Several small molecule DYRK1A inhibitors have been identified that induce human β-cell proliferation in vitro and in vivo. Furthermore, DYRK1A inhibitors have also been shown to synergize β-cell proliferation with other classes of drugs, such as TGFβ inhibitors and GLP-1 receptor agonists. In this perspective, we review the status of DYRK1A as a therapeutic target for β-cell proliferation and provide perspectives on technical and scientific challenges for future translational development.
- Subjects :
- Animals
Diabetes Mellitus metabolism
Drug Discovery
Humans
Insulin-Secreting Cells cytology
Insulin-Secreting Cells metabolism
Protein Kinase Inhibitors chemistry
Protein Serine-Threonine Kinases metabolism
Protein-Tyrosine Kinases metabolism
Dyrk Kinases
Cell Proliferation drug effects
Diabetes Mellitus drug therapy
Insulin-Secreting Cells drug effects
Protein Kinase Inhibitors pharmacology
Protein Serine-Threonine Kinases antagonists & inhibitors
Protein-Tyrosine Kinases antagonists & inhibitors
Subjects
Details
- Language :
- English
- ISSN :
- 1520-4804
- Volume :
- 64
- Issue :
- 6
- Database :
- MEDLINE
- Journal :
- Journal of medicinal chemistry
- Publication Type :
- Academic Journal
- Accession number :
- 33682417
- Full Text :
- https://doi.org/10.1021/acs.jmedchem.0c02050