DYRK1A型
神经退行性变
高磷酸化
激酶
化学
发病机制
疾病
癌症研究
生物
生物化学
医学
免疫学
内科学
作者
Tong Liu,Yuxi Wang,Jiaxing Wang,Changyu Ren,Hao Chen,Jifa Zhang
标识
DOI:10.1016/j.ejmech.2021.114062
摘要
Dual-specificity tyrosine phosphorylation-regulated kinase 1 A (DYRK1A) is a conserved protein kinase that plays essential roles in various biological processes. It is located in the region q22.2 of chromosome 21, which is involved in the pathogenesis of Down syndrome (DS). Moreover, DYRK1A has been shown to promote the accumulation of amyloid beta (Aβ) peptides leading to gradual Tau hyperphosphorylation, which contributes to neurodegeneration. Additionally, alterations in the DRK1A expression are also associated with cancer and diabetes. Recent years have witnessed an explosive increase in the development of DYRK1A inhibitors. A variety of novel DYRK1A inhibitors have been reported as potential treatments for human diseases. In this review, the latest therapeutic potential of DYRK1A for different diseases and the novel DYRK1A inhibitors discoveries are summarized, guiding future inhibitor development and structural optimization.
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