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.

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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