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胰岛素样生长因子-1受体(IGF-1R)抑制可增强放射敏感性,并通过非同源末端连接和同源重组两种方式延迟双链断裂修复。

IGF-1R inhibition enhances radiosensitivity and delays double-strand break repair by both non-homologous end-joining and homologous recombination.

作者信息

Chitnis M M, Lodhia K A, Aleksic T, Gao S, Protheroe A S, Macaulay V M

机构信息

1] Department of Oncology Laboratories, Weatherall Institute of Molecular Medicine, John Radcliffe Hospital, University of Oxford, Oxford, UK [2] Department of Oncology, Cancer and Haematology Centre, The Churchill Hospital, Oxford, UK.

Department of Oncology Laboratories, Weatherall Institute of Molecular Medicine, John Radcliffe Hospital, University of Oxford, Oxford, UK.

出版信息

Oncogene. 2014 Nov 6;33(45):5262-73. doi: 10.1038/onc.2013.460. Epub 2013 Nov 4.

Abstract

Inhibition of type 1 insulin-like growth factor receptor (IGF-1R) enhances tumor cell sensitivity to ionizing radiation. It is not clear how this effect is mediated, nor whether this approach can be applied effectively in the clinic. We previously showed that IGF-1R depletion delays repair of radiation-induced DNA double-strand breaks (DSBs), unlikely to be explained entirely by reduction in homologous recombination (HR) repair. The current study tested the hypothesis that IGF-1R inhibition induces a repair defect that involves non-homologous end joining (NHEJ). IGF-1R inhibitor AZ12253801 blocked cell survival and radiosensitized IGF-1R-overexpressing murine fibroblasts but not isogenic IGF-1R-null cells, supporting specificity for IGF-1R. IGF-1R inhibition enhanced radiosensitivity in DU145, PC3 and 22Rv1 prostate cancer cells, comparable to effects of Ataxia Telangiectasia Mutated inhibition. AZ12253801-treated DU145 cells showed delayed resolution of γH2AX foci, apparent within 1 h of irradiation and persisting for 24 h. In contrast, IGF-1R inhibition did not influence radiosensitivity or γH2AX focus resolution in LNCaP-LN3 cells, suggesting that radiosensitization tracks with the ability of IGF-1R to influence DSB repair. To differentiate effects on repair from growth and cell-survival responses, we tested AZ12253801 in DU145 cells at sub-SF50 concentrations that had no early (⩽48 h) effects on cell cycle distribution or apoptosis induction. Irradiated cultures contained abnormal mitoses, and after 5 days IGF-1R-inhibited cells showed enhanced radiation-induced polyploidy and nuclear fragmentation, consistent with the consequences of entry into mitosis with incompletely repaired DNA. AZ12253801 radiosensitized DNA-dependent protein kinase (DNA-PK)-proficient but not DNA-PK-deficient glioblastoma cells, and did not radiosensitize DNA-PK-inhibited DU145 cells, suggesting that in the context of DSB repair, IGF-1R functions in the same pathway as DNA-PK. Finally, IGF-1R inhibition attenuated repair by both NHEJ and HR in HEK293 reporter assays. These data indicate that IGF-1R influences DSB repair by both major DSB repair pathways, findings that may inform clinical application of this approach.

摘要

抑制1型胰岛素样生长因子受体(IGF-1R)可增强肿瘤细胞对电离辐射的敏感性。目前尚不清楚这种效应是如何介导的,也不清楚这种方法能否在临床上有效应用。我们之前的研究表明,IGF-1R的缺失会延迟辐射诱导的DNA双链断裂(DSB)的修复,这不太可能完全由同源重组(HR)修复的减少来解释。本研究检验了一个假设,即IGF-1R抑制会诱导一种涉及非同源末端连接(NHEJ)的修复缺陷。IGF-1R抑制剂AZ12253801可阻断细胞存活并使过表达IGF-1R的小鼠成纤维细胞对辐射敏感,但对同基因IGF-1R缺失的细胞无效,这支持了其对IGF-1R的特异性。IGF-1R抑制增强了DU145、PC3和22Rv1前列腺癌细胞的辐射敏感性,与共济失调毛细血管扩张突变抑制的效果相当。用AZ12253801处理的DU145细胞显示γH2AX焦点的消退延迟,在照射后1小时内明显,并持续24小时。相比之下,IGF-1R抑制对LNCaP-LN3细胞的辐射敏感性或γH2AX焦点消退没有影响,这表明辐射增敏与IGF-1R影响DSB修复的能力相关。为了区分对修复的影响与生长和细胞存活反应,我们在低于半数致死浓度(SF50)的情况下,在DU145细胞中测试了AZ12253801,该浓度对细胞周期分布或凋亡诱导没有早期(⩽48小时)影响。照射后的培养物中出现异常有丝分裂,5天后,IGF-1R抑制的细胞显示辐射诱导的多倍体和核碎裂增强,这与未完全修复的DNA进入有丝分裂的后果一致。AZ12253801使DNA依赖蛋白激酶(DNA-PK)功能正常的胶质母细胞瘤细胞对辐射敏感,但对DNA-PK缺陷的细胞无效,并且不会使DNA-PK抑制的DU145细胞对辐射敏感,这表明在DSB修复的背景下,IGF-1R与DNA-PK在同一途径中发挥作用。最后,在HEK293报告基因试验中,IGF-1R抑制减弱了NHEJ和HR的修复。这些数据表明,IGF-1R通过两种主要的DSB修复途径影响DSB修复,这些发现可能为该方法的临床应用提供参考。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c18f/3997348/d2b55cc4c331/emss-56055-f0001.jpg

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