| Literature DB >> 31376410 |
Pengfei Xu1, Chiara Ianes2, Fabian Gärtner3, Congxing Liu4, Timo Burster5, Vasiliy Bakulev6, Najma Rachidi7, Uwe Knippschild8, Joachim Bischof9.
Abstract
Members of the highly conserved pleiotropic CK1 family of serine/threonine-specific kinases are tightly regulated in the cell and play crucial regulatory roles in multiple cellular processes from protozoa to human. Since their dysregulation as well as mutations within their coding regions contribute to the development of various different pathologies, including cancer and neurodegenerative diseases, they have become interesting new drug targets within the last decade. However, to develop optimized CK1 isoform-specific therapeutics in personalized therapy concepts, a detailed knowledge of the regulation and functions of the different CK1 isoforms, their various splice variants and orthologs is mandatory. In this review we will focus on the stress-induced CK1 isoform delta (CK1δ), thereby addressing its regulation, physiological functions, the consequences of its deregulation for the development and progression of diseases, and its potential as therapeutic drug target.Entities:
Keywords: CSNK1D; Cancer; Casein kinase 1; Hedgehog pathway; N; P; Phosphorylation; R; S; Site-specific phosphorylation; Small molecule inhibitor; Stress-induced kinase; Wnt signaling pathway; p53
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Year: 2019 PMID: 31376410 PMCID: PMC7939460 DOI: 10.1016/j.gene.2019.144005
Source DB: PubMed Journal: Gene ISSN: 0378-1119 Impact factor: 3.688