cx-4945 and Down-Syndrome

DYRK1A is important in neuronal development and function, and its excessive activity is considered a significant pathogenic factor in Down syndrome and Alzheimer's disease. Thus, inhibition of DYRK1A has been suggested to be a new strategy to modify the disease. Very few compounds, however, have been reported to act as inhibitors, and their potential clinical uses require further evaluation. Here, we newly identify CX-4945, the safety of which has been already proven in the clinical setting, as a potent inhibitor of DYRK1A that acts in an ATP-competitive manner. The inhibitory potency of CX-4945 on DYRK1A (IC50=6.8 nM) in vitro was higher than that of harmine, INDY or proINDY, which are well-known potent inhibitors of DYRK1A. CX-4945 effectively reverses the aberrant phosphorylation of Tau, amyloid precursor protein (APP) and presenilin 1 (PS1) in mammalian cells. To our surprise, feeding with CX-4945 significantly restored the neurological and phenotypic defects induced by the overexpression of minibrain, an ortholog of human DYRK1A, in the Drosophila model. Moreover, oral administration of CX-4945 acutely suppressed Tau hyperphosphorylation in the hippocampus of DYRK1A-overexpressing mice. Our research results demonstrate that CX-4945 is a potent DYRK1A inhibitor and also suggest that it has therapeutic potential for DYRK1A-associated diseases.

Topics: Adenosine Triphosphate; Administration, Oral; Alzheimer Disease; Amyloid beta-Protein Precursor; Animals; Calcineurin; Disease Models, Animal; Down Syndrome; Drosophila melanogaster; HEK293 Cells; Hippocampus; Humans; Mice, Inbred C57BL; Models, Molecular; Naphthyridines; Neurons; NFATC Transcription Factors; Phenazines; Phenotype; Phosphorylation; Presenilin-1; Protein Kinase Inhibitors; Protein Serine-Threonine Kinases; Signal Transduction; tau Proteins