Qi Lin, Zhang Yang
Department of Orthodontics, School of Stomatology, China Medical University; Liaoning Institute of Dental Research, Shenyang, 110002, Liaoning, People's Republic of China.
Tumour Biol. 2015 Mar;36(3):1797-802. doi: 10.1007/s13277-014-2782-3. Epub 2014 Nov 4.
Aurora-A kinases are overexpressed in many cancer tissues and cells. Alisertib is an investigational, orally administered, selective, small-molecule Aurora-A kinase inhibitor with preclinical activity against a broad range of tumors. Our study was aimed to detect the effects of alisertib on human tongue squamous cell carcinoma (HTSCC). Treatment of a human tongue squamous cell carcinoma cell line, HSC-3, with alisertib to inhibition of Aurora-A kinases reduced proliferation and induced apoptosis, which was accompanied by activation of the ATM/Chk2/p53 pathway. In vivo, inhibition of Aurora-A kinases in established xenografted tumors decreased tumor size and weight. Kaplan-Meyer survival analysis demonstrated that the cumulative survival time of mice without Aurora-A kinases was significantly longer than those with Aurora-A kinases. Our data provide the basis for developing alisertib to treat human tongue squamous cell carcinoma.
极光激酶A在许多癌症组织和细胞中过度表达。阿利塞替布是一种正在研究的口服、选择性小分子极光激酶A抑制剂,对多种肿瘤具有临床前活性。我们的研究旨在检测阿利塞替布对人舌鳞状细胞癌(HTSCC)的影响。用阿利塞替布处理人舌鳞状细胞癌细胞系HSC-3以抑制极光激酶A,可减少细胞增殖并诱导凋亡,同时伴有ATM/Chk2/p53通路的激活。在体内,对已建立的异种移植肿瘤中极光激酶A的抑制可减小肿瘤大小和重量。Kaplan-Meier生存分析表明,没有极光激酶A的小鼠的累积生存时间明显长于有极光激酶A的小鼠。我们的数据为开发阿利塞替布治疗人舌鳞状细胞癌提供了依据。