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阿利西替尼(MLN8237)是一种选择性极光激酶A抑制剂,在体外和体内均可诱导人舌鳞状细胞癌细胞凋亡。

Alisertib (MLN8237), a selective Aurora-A kinase inhibitor, induces apoptosis in human tongue squamous cell carcinoma cell both in vitro and in vivo.

作者信息

Qi Lin, Zhang Yang

机构信息

Department of Orthodontics, School of Stomatology, China Medical University; Liaoning Institute of Dental Research, Shenyang, 110002, Liaoning, People's Republic of China.

出版信息

Tumour Biol. 2015 Mar;36(3):1797-802. doi: 10.1007/s13277-014-2782-3. Epub 2014 Nov 4.

Abstract

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.

摘要

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。

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