Targeting AURKA in Cancer: molecular mechanisms and opportunities for Cancer therapy

被引:0
作者
Ruijuan Du
Chuntian Huang
Kangdong Liu
Xiang Li
Zigang Dong
机构
[1] School of Basic Medical Sciences,Department of Pathophysiology
[2] Zhengzhou University,State Key Laboratory of Esophageal Cancer Prevention and Treatment
[3] China-US (Henan) Hormel Cancer Institute,undefined
[4] The Collaborative Innovation Center of Henan Province for Cancer Chemoprevention,undefined
[5] Zhengzhou University,undefined
[6] College of medicine,undefined
[7] Zhengzhou University,undefined
来源
Molecular Cancer | / 20卷
关键词
Aurora kinase a; Cancer; Regulators; Substrates; Inhibitors; Combination therapy;
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摘要
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.
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