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Function and inhibition of DYRK1A: Emerging roles of treating multiple human diseases
Yuping Yang1, Xiaoxiao Fan1, Yongjian Liu1
1School of Chinese Materia Medica, Beijing University of Chinese Medicine, Beijing 102488, China.
Abstract:
Dual-specificity tyrosine phosphorylation-regulated kinase 1A (DYRK1A) is an evolutionarily conserved protein kinase and the most studied member of the Dual-specificity tyrosine-regulated kinase (DYRK) family. It has been shown that it participates in the development of plenty of diseases, and both the low or high expression of DYRK1A protein could lead to disorder. Thus, DYRK1A is recognized as a key target for the therapy for these diseases, and the studies on natural or synthetic DYRK1A inhibitors have become more and more popular. Here, we provide a comprehensive review for DYRK1A from the structure and function of DYRK1A, the roles of DYRK1A in various types of diseases, including diabetes mellitus, neurodegenerative diseases, and kinds of cancers, and the studies of its natural and synthetic inhibitors.
Insights
Dual-specificity tyrosine phosphorylation-regulated kinase 1A (DYRK1A) is crucial in disease development. This review covers DYRK1A
Area of Science:
- Biochemistry and Molecular Biology
- Cell Signaling
- Disease Pathogenesis
Background:
- Dual-specificity tyrosine phosphorylation-regulated kinase 1A (DYRK1A) is a key protein kinase involved in numerous cellular processes.
- Aberrant DYRK1A expression, either low or high, is linked to the pathogenesis of various diseases.
- DYRK1A is recognized as a significant therapeutic target for multiple disorders.
Purpose of the Study:
- To provide a comprehensive review of DYRK1A.
- To elucidate the structure, function, and disease relevance of DYRK1A.
- To summarize the landscape of DYRK1A inhibitors.
Main Methods:
- Literature review of existing research on DYRK1A.
- Analysis of studies detailing DYRK1A's role in disease.
- Compilation of data on natural and synthetic DYRK1A inhibitors.
Main Results:
- DYRK1A's involvement in diabetes mellitus, neurodegenerative diseases, and cancers is detailed.
- The review categorizes and discusses various natural and synthetic DYRK1A inhibitors.
- Structure-function relationships and disease mechanisms associated with DYRK1A are explored.
Conclusions:
- DYRK1A is a critical regulator implicated in diverse pathologies.
- Targeting DYRK1A with inhibitors presents a promising therapeutic strategy.
- Further research into DYRK1A inhibitors is warranted for disease treatment.
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