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通过产生无着丝粒微核实现 ATR 抑制剂 AZD6738 的放射增敏作用。

Radiosensitization by the ATR Inhibitor AZD6738 through Generation of Acentric Micronuclei.

作者信息

Dillon Magnus T, Barker Holly E, Pedersen Malin, Hafsi Hind, Bhide Shreerang A, Newbold Kate L, Nutting Christopher M, McLaughlin Martin, Harrington Kevin J

机构信息

Targeted Therapy Team, Division of Radiotherapy and Imaging, The Institute of Cancer Research, London, UK.

The Royal Marsden Hospital, London, UK.

出版信息

Mol Cancer Ther. 2017 Jan;16(1):25-34. doi: 10.1158/1535-7163.MCT-16-0239. Epub 2016 Nov 9.

Abstract

AZD6738 is an orally active ATR inhibitor (ATRi) currently in phase I clinical trials. We found in vitro growth inhibitory activity of this ATRi in a panel of human cancer cell lines. We demonstrated radiosensitization by AZD6738 to single radiation fractions in multiple cancer cell lines independent of both p53 and BRCA2 status by the clonogenic assay. Radiosensitization by AZD6738 to clinically relevant doses of fractionated radiation was demonstrated in vitro using a 3D tumor spheroid model and, in vivo, AZD6738 radiosensitized by abrogating the radiation-induced G cell-cycle checkpoint and inhibiting homologous recombination. Mitosis with damaged DNA resulted in mitotic catastrophe as measured by micronucleus formation by live-cell fluorescent-ubiquitination cell-cycle imaging of cell-cycle progression and nuclear morphology. Induction of micronuclei was significantly more prominent for AZD6738 compared with inhibition of the downstream kinase CHK1 alone at isoeffective doses. Micronuclei were characterized as acentric chromosomal fragments, which displayed characteristics of increased DNA damage and cell-cycle dyssynchrony when compared with the primary nucleus. Mol Cancer Ther; 16(1); 25-34. ©2016 AACR.

摘要

AZD6738是一种口服活性的共济失调毛细血管扩张症突变基因(ATR)抑制剂(ATRi),目前正处于I期临床试验阶段。我们发现这种ATRi在一组人类癌细胞系中具有体外生长抑制活性。通过克隆形成试验,我们证明了AZD6738在多种癌细胞系中对单次放射剂量具有放射增敏作用,且与p53和BRCA2状态无关。使用三维肿瘤球体模型在体外证明了AZD6738对临床相关分次放射剂量具有放射增敏作用,并且在体内,AZD6738通过消除辐射诱导的G2期细胞周期检查点和抑制同源重组而产生放射增敏作用。通过对细胞周期进程和细胞核形态进行活细胞荧光泛素化细胞周期成像来测量微核形成,结果显示,有受损DNA的有丝分裂会导致有丝分裂灾难。在等效剂量下,与单独抑制下游激酶CHK1相比,AZD6738诱导的微核明显更为突出。微核被鉴定为无着丝粒染色体片段,与主核相比,其显示出DNA损伤增加和细胞周期不同步的特征。《分子癌症治疗》;16(1);25 - 34。©2016美国癌症研究协会。

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