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首页> 外文期刊>Radiation and Environmental Biophysics >Radiosensitization of NSCLC cells to X-rays and carbon ions by the CHK1/CHK2 inhibitor AZD7762, Honokiol and Tunicamycin
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Radiosensitization of NSCLC cells to X-rays and carbon ions by the CHK1/CHK2 inhibitor AZD7762, Honokiol and Tunicamycin

机译:CHK1 / CHK2抑制剂AZD7762,HONOKIOL和Tunicamycin的NSCLC细胞对X射线和碳离子的辐射敏化

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摘要

Although radiotherapy, especially carbon-ion radiotherapy, is an effective treatment modality against non-small-cell lung cancer (NSCLC), studies using radiation combined with sensitizer for improving the efficacy of radiotherapy are still needed. In this work, we aimed to investigate in NSCLC A549 and H1299 cell lines the effects of different linear energy transfer (LET) radiations combined with diverse sensitizing compounds. Cells pretreated with the CHK1/CHK2 inhibitor AZD7762, Honokiol or Tunicamycin were irradiated with low-LET X-rays and high-LET carbon ions. Cell survival was assessed using the clonogenic cell survival assay. Cell cycle distribution and apoptosis were measured with flow cytometry, and DNA double strand break (DSB) and repair were detected using gamma-H2AX immunofluorescence staining. Our results revealed that AZD7762, Honokiol and Tunicamycin demonstrated low cytotoxicity to NSCLC cells and a pronounced radiosensitizing effect on NSCLC cells exposed to carbon ions than X-rays. Unrepaired DNA DSB damages, the abrogation of G2/M arrest induced by irradiation, and finally apoptotic cell death were the main causes of the radiosensitizing effect. Thus, our data suggest that high-LET carbon ion combined with these compounds may be a potentially effective therapeutic strategy for locally advanced NSCLC.
机译:虽然放射疗法,尤其是碳离子放射疗法,是针对非小细胞肺癌(NSCLC)的有效治疗方式,但仍然需要使用辐射与敏感剂改善放射疗法效果的研究。在这项工作中,我们旨在研究NSCLC A549和H1299细胞系不同的线性能量转移(让)辐射与多样化敏化化合物的影响。用低使X射线和高碳离子照射用CHK1 / CHK2抑制剂AZD7762预处理的细胞,檀香或叔霉素。使用克隆核化细胞存活测定评估细胞存活。用流式细胞术测量细胞周期分布和细胞凋亡,使用γ-H2AX免疫荧光染色检测DNA双链断裂(DSB)和修复。我们的结果表明,AZD7762,HONOKIOL和TUNICAMICIN对NSCLC细胞的低细胞毒性和对暴露于碳离子的NSCLC细胞的显着放射敏感性效果而不是X射线。未解发的DNA DNA DSB损坏,辐射诱导的G2 / M停滞的损失,最终凋亡细胞死亡是放射敏化效应的主要原因。因此,我们的数据表明,与这些化合物相结合的高使碳离子可以是局部晚期NSCLC的潜在有效的治疗策略。

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