首页> 外文期刊>Thoracic cancer. >ANTP‐SmacN7 fusion peptide‐induced radiosensitization in A549 cells and its potential mechanisms
【24h】

ANTP‐SmacN7 fusion peptide‐induced radiosensitization in A549 cells and its potential mechanisms

机译:ANTP-SMACN7融合肽诱导A549细胞的辐射敏化和其潜在机制

获取原文
           

摘要

BACKGROUND:Radioresistance in tumors limits the curative effect of the radiotherapy. Mimetic compounds of second mitochondria-derived activator of caspase (Smac) are potential new tumor radiation-sensitizing drugs because they can increase radiation-induced tumor cell apoptosis. Here, we observed the radiosensitization effect of a new Smac mimetic Antennapedia protein (ANTP)-SmacN7 fusion peptide in A549 cells and investigated the underlying mechanisms behind the effects of this protein on tumor cells.METHODS:The ANTP-SmacN7 fusion peptide was synthesized and linked with fluorescein isothiocyanate to observe the protein's ability to penetrate cells. A549 cells were divided into the control, radiation-only, ANTP-SmacN7-only and ANTP-SmacN7? ?radiation groups. The cells were exposed to 0, 2, 4 and 6 Gy, with 20 μmol/L of ANTP-SmacN7. The radiation-sensitizing effects of the ANTP-SmacN7 fusion proteins were observed via clonogenic assay. Apoptosis was detected using flow cytometry. A comet assay was used to assess DNA damage. The levels and degrees of cytochrome-c, PARP, H2AX, caspase-8, caspase-3, and caspase-9 activation were detected via western blot assay. The radiation sensitization of the fusion peptide, expression of γ-H2AX and C-PARP were compared after adding the caspase inhibitor, Z-VAD.RESULTS:ANTP-SmacN7 fusion proteins entered the cells and promoted A549 cell radiosensitization. Treatment with ANTP-SmacN7? ?radiation significantly reduced the A549 cell clone-forming rate, increased the cytochrome-c, cleaved caspase-8, cleaved caspase-3 and cleaved caspase-9 expression levels, promoted caspase activation, and increased the rate of radiation-induced apoptosis. The ANTP-SmacN7 fusion peptide significantly increased radiation-induced double-stranded DNA rupture in the A549 cells and increased DNA damage. Adding Z-VAD reduced the fusion peptide's proapoptotic effect but not the level of double-stranded DNA breakage.CONCLUSIONS:The ANTP-SmacN7 fusion peptide exerted a remarkable radiosensitization effect on A549 cells. This protein may reduce tumor cell radioresistance by inducing caspase activation and may be a potential new Smac mimetic that can be applied in radiosensitization therapy.? 2020 The Authors. Thoracic Cancer published by China Lung Oncology Group and John Wiley & Sons Australia, Ltd.
机译:背景:肿瘤的辐射敏感度限制了放射疗法的疗效。 Caspase(SMAC)的第二线粒体衍生激活剂的模拟化合物是潜在的新肿瘤辐射致敏药物,因为它们可以增加辐射诱导的肿瘤细胞凋亡。在这里,我们观察到A549细胞中新SMAC模拟天平蛋白(ANTP)-SmacN7融合肽的放射敏化效应,并研究了该蛋白质对肿瘤细胞的影响背后的潜在机制。方法:合成抗蛋白酶肽肽与荧光素相连,异硫氰酸酯观察蛋白质的渗透细胞的能力。 A549细胞分为对照,仅辐射,禁区,仅限SMACN7和ANTP-SMACN7? ?辐射组。将细胞暴露于0,2,4和6Gy,用20μmol/ L的抗乳酸SmacN7。通过克隆基测定观察AntP-Smacn7融合蛋白的辐射敏化效应。使用流式细胞术检测细胞凋亡。使用彗星测定来评估DNA损伤。通过蛋白质印迹测定检测细胞色素-C,PARP,H2AX,Caspase-8,Caspase-3和Caspase-9的水平和程度。在添加Caspase抑制剂Z-VAD后比较融合肽的辐射敏化,γ-H2AX和C-PARP的表达:抗体进入细胞并促进了A549细胞辐射敏化蛋白。用antp-smacn7治疗? ?辐射显着降低了A549细胞克隆成型率,增加了细胞色素-C,切割的caspase-8,切割的caspase-3和切割的caspase-9表达水平,促进了胱天蛋白激活,增加了辐射诱导的细胞凋亡的速率。 ANTP-SMACN7融合肽显着增加了A549细胞中的辐射诱导的双链DNA破裂并增加了DNA损伤。添加Z-VAD降低了融合肽的促进效应,但不是双链DNA破裂的水平。结论:抗蛋白酶掺杂肽对A549细胞产生显着的放射敏化效应。通过诱导胱天蛋白酶激活,该蛋白质可以减少肿瘤细胞辐射敏感度,并且可以是可用于放射敏化疗法的潜在新的SMAC模拟物。 2020作者。中国肺部肿瘤集团和约翰瓦里和儿子澳大利亚发表的胸癌

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号