| Literature DB >> 33682417 |
Kunal Kumar1, Chalada Suebsuwong1, Peng Wang2, Adolfo Garcia-Ocana2, Andrew F Stewart2, Robert J DeVita1.
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.Entities:
Mesh:
Substances:
Year: 2021 PMID: 33682417 DOI: 10.1021/acs.jmedchem.0c02050
Source DB: PubMed Journal: J Med Chem ISSN: 0022-2623 Impact factor: 7.446