极光抑制剂
极光激酶
极光激酶B
极光A激酶
激酶
细胞周期蛋白依赖激酶4
医学
癌症研究
生物
癌症
MAP激酶激酶激酶
蛋白激酶A
细胞周期
细胞生物学
主轴装置
生物化学
细胞
内科学
细胞分裂
作者
Xue-Li Jing,Shi‐Wu Chen
标识
DOI:10.1080/13543776.2021.1890027
摘要
Introduction: Aurora kinases are a family of serine/threonine kinases, and promote mitotic spindle assembly by regulating centrosome duplication and separation. Aurora kinases are overexpressed in a variety of tumor cell lines, thus, the use of Aurora kinase small-molecule inhibitors has become a potential treatment option for cancer.Areas covered: As a continuing review of Aurora kinase inhibitors and their patents published in 2009, 2011 and 2014. Herein, we updated the information for Aurora kinase inhibitors in clinical trials and the patents filed from 2014 to 2020. PubMed, Scopus, SciFinder, and www.clinicaltrials.gov databases were used for searching the clinical information and patents of Aurora kinase inhibitors.Expert opinion: Even though Aurora A or B selective as well as pan inhibitors show preclinical and clinical efficacy, so far, no Aurora kinase inhibitor has been approved for clinical use. Preliminary evidence suggested that highly selective Aurora kinase or multi-target inhibitors as a single agent as well as in combination therapy are still the current main development trend of Aurora kinase inhibitors.
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