| Literature DB >> 33451333 |
Ruijuan Du1,2, Chuntian Huang3,4, Kangdong Liu3,4,5,6, Xiang Li7,8,9,10, Zigang Dong11,12,13,14,15.
Abstract
Aurora kinase A (AURKA) belongs to the family of serine/threonine kinases, whose activation is necessary for cell division processes via regulation of mitosis. AURKA shows significantly higher expression in cancer tissues than in normal control tissues for multiple tumor types according to the TCGA database. Activation of AURKA has been demonstrated to play an important role in a wide range of cancers, and numerous AURKA substrates have been identified. AURKA-mediated phosphorylation can regulate the functions of AURKA substrates, some of which are mitosis regulators, tumor suppressors or oncogenes. In addition, enrichment of AURKA-interacting proteins with KEGG pathway and GO analysis have demonstrated that these proteins are involved in classic oncogenic pathways. All of this evidence favors the idea of AURKA as a target for cancer therapy, and some small molecules targeting AURKA have been discovered. These AURKA inhibitors (AKIs) have been tested in preclinical studies, and some of them have been subjected to clinical trials as monotherapies or in combination with classic chemotherapy or other targeted therapies.Entities:
Keywords: Aurora kinase a; Cancer; Combination therapy; Inhibitors; Regulators; Substrates
Year: 2021 PMID: 33451333 PMCID: PMC7809767 DOI: 10.1186/s12943-020-01305-3
Source DB: PubMed Journal: Mol Cancer ISSN: 1476-4598 Impact factor: 27.401