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靶向 Aurora 激酶 A 增强非典型畸胎样横纹肌样瘤细胞的辐射敏感性。

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

机构信息

Department of Pediatrics, Children's Hospital Colorado, University of Colorado School of Medicine, Anschutz Medical Campus, Aurora, CO, USA.

出版信息

J Neurooncol. 2012 May;107(3):517-26. doi: 10.1007/s11060-011-0795-y. Epub 2012 Jan 15.

Abstract

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.

摘要

非典型畸胎样/横纹肌样瘤(ATRT)是一种罕见的、高度恶性的胚胎性中枢神经系统肿瘤,预后较差。治疗依赖于高度毒性的化疗和放疗。为了改善结果并降低发病率,需要更有针对性的治疗。基因表达分析显示,ATRT 组织中多种激酶的表达升高。Aurora Kinase A 是候选激酶之一。本研究的目的是评估 Aurora Kinase A 抑制对 ATRT 细胞系的影响。我们的分析表明,Aurora Kinase A 的抑制可诱导 ATRT 细胞死亡,并且小分子抑制剂 MLN 8237 可使这些细胞对辐射敏感。此外,Aurora Kinase A 的抑制导致促增殖信号通路活性降低。这些数据表明,抑制 Aurora Kinase A 是 ATRT 治疗的一个有前途的小分子靶标。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/908a/4681522/2c3a6d6bc1b4/nihms742747f1.jpg

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