Targeting Aurora Kinase A enhances radiation sensitivity of atypical teratoid rhabdoid tumor cells

被引:53
|
作者
Venkataraman, Sujatha [2 ]
Alimova, Irina [2 ]
Tello, Tiffany [3 ]
Harris, Peter S. [2 ]
Knipstein, Jeffrey A. [2 ]
Donson, Andrew M. [2 ]
Foreman, Nicholas K. [2 ]
Liu, Arthur K. [4 ]
Vibhakar, Rajeev [1 ,2 ]
机构
[1] Univ Colorado, Dept Pediat, Aurora, CO 80045 USA
[2] Univ Colorado, Sch Med, Dept Pediat, Childrens Hosp Colorado, Aurora, CO USA
[3] Univ Colorado, Sch Med, Aurora, CO 80045 USA
[4] Univ Colorado, Dept Radiat Oncol, Aurora, CO 80045 USA
基金
美国国家卫生研究院;
关键词
Atypical teratoid rhabdoid tumor; ATRT; Aurora Kinase A; CENTRAL-NERVOUS-SYSTEM; TERATOID/RHABDOID TUMORS; A EXPRESSION; CANCER; CHILDREN; AMPLIFICATION; INHIBITION; THERAPY; GENE;
D O I
10.1007/s11060-011-0795-y
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Atypical teratoid/ rhabdoid tumors (ATRT) are rare, highly malignant, embryonal CNS tumors with a poor prognosis. Therapy relies on highly toxic chemotherapy and radiotherapy. To improve outcomes and decrease morbidity, more targeted therapy is required. Gene expression analysis revealed elevated expression of multiple kinases in ATRT tissues. Aurora Kinase A was one of the candidate kinases. The objective of this study was to evaluate the impact of Aurora Kinase A inhibition in ATRT cell lines. Our analysis revealed that inhibition of Aurora Kinase A induces cell death in ATRT cells and the small molecule inhibitor MLN 8237 sensitizes these cells to radiation. Furthermore, inhibition of Aurora Kinase A resulted in decreased activity of pro-proliferative signaling pathways. These data indicate that inhibition of Aurora Kinase A is a promising small molecule target for ATRT therapy.
引用
收藏
页码:517 / 526
页数:10
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