方政,袁惠芳,赵军方,孙明磊,乔彬,吴大鹏,李新明,孙强.沉默EZH2诱导舌癌Tca-8113细胞凋亡及其对放射敏感性的影响[J].中华放射医学与防护杂志,2018,38(8):561-566
沉默EZH2诱导舌癌Tca-8113细胞凋亡及其对放射敏感性的影响
Effects of EZH2 siRNA on apoptosis induction and radiosensitivity of tongue cancer Tca-8113 cells
投稿时间:2018-01-27  
DOI:10.3760/cma.j.issn.0254-5098.2018.08.001
中文关键词:  舌鳞癌  放疗  凋亡  EZH2
英文关键词:Tongue squamous cell carcinoma  Radiotherapy  Apoptosis  EZH2
基金项目:国家自然科学基金(8140100298)
作者单位E-mail
方政 450052 郑州大学第一附属医院口腔颌面外科  
袁惠芳 450052 郑州大学第一附属医院口腔颌面外科  
赵军方 450052 郑州大学第一附属医院口腔颌面外科 junfangzhao@zzu.edu.cn 
孙明磊 450052 郑州大学第一附属医院口腔颌面外科  
乔彬 450052 郑州大学第一附属医院口腔颌面外科  
吴大鹏 475000 开封, 河南大学淮河医院放疗科  
李新明 450052 郑州大学第一附属医院口腔颌面外科  
孙强 450052 郑州大学第一附属医院口腔颌面外科  
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中文摘要:
      目的 探讨zeste基因增强子同源物2(enhancer of zeste homolog 2,EZH2)对舌鳞癌细胞凋亡及放射敏感性的影响。方法 以舌鳞癌Tca-8113细胞为研究对象,细胞转染EZH2小干扰RNA(EZH2 siRNA1、EZH2 siRNA2)及小干扰RNA阴性对照(siRNA-NC),RT-PCR和Western blot检测EZH2表达水平,筛选干扰效果较好的EZH2 siRNA2继续研究。将转染EZH2 siRNA2后的Tca-8113记为EZH2 siRNA2组,同时以不做处理的细胞为对照组,用8 Gy剂量照射转染siRNA对照组和EZH2 siRNA2细胞,并依次命名为照射组和联合组,四甲基偶氮唑盐(MTT)检测细胞增殖,流式细胞术检测细胞凋亡,Western blot检测信号转导与转录因子3(STAT3)、磷酸化的STAT3(p-STAT3)、活性Caspase-3(Cleaved Caspase-3)表达。siRNA-NC组和EZH2 siRNA2组细胞用0、2、4、6、8 Gy剂量照射处理后,细胞克隆实验检测放射敏感性。结果 EZH2 siRNA1、EZH2 siRNA2均能够干扰舌鳞癌细胞中EZH2的表达,且EZH2 siRNA2干扰效果最好(tmRNA=8.660,PmRNA<0.01;t蛋白=2.883,P蛋白<0.05)。下调EZH2 siRNA2组细胞凋亡率为(29.90±1.64)%,联合组凋亡率为(38.17±1.59)%,二者比较,差异有统计学意义(t=4.742,P<0.05),同时下调EZH2还可以降低p-STAT3水平,促进Cleaved Caspase-3蛋白表达。干扰EZH2表达后Tca-8113细胞辐射增敏比为1.668。结论 干扰EZH2表达能够协同放疗促进舌鳞癌细胞凋亡,抑制舌鳞癌细胞增殖,增加舌鳞癌细胞放射敏感性。
英文摘要:
      Objective To investigate the effect of EZH2 on apoptosis and radiosensitivity of squamous cell carcinoma of tongue.Methods Tongue squamous carcinoma cells Tca-8113 were transfected with small interfering RNA of EZH2 (EZH2 siRNA1, EZH2 siRNA2) and its negative controls (siRNA-NC), the expression levels of EZH2 were detected by RT-PCR and Western blot and EZH2 siRNA2 was used for further studied since its better interference efficiency. The cells with siRNA transfection were irradiated with 8 Gy doses, and cell proliferation was detected by MTT, apoptosis was detected by flow cytometry, the expression of p-STAT3, STAT3 and Cleaved Caspase-3 was detected by Western blot. In addition, the cells were irradiated with 0, 2, 4, 6, and 8 Gy to detect radiosensitivity by cell colony formation assay.Results EZH2 siRNA1 and EZH2 siRNA2 decreased the expression of EZH2 in Tca-8113 cells and EZH2 siRNA2 had a better interference efficiency (tmRNA=8.660, PmRNA<0.01; tprotein=2.883, Pprotein<0.05). The apoptotic rate in the EZH2 siRNA group was (29.90±1.64)%, and was increased by 8 Gy irradiation to (38.17±1.59)% (t=4.742, P<0.05). At the same time, EZH2 siRNA reduced the level of p-STAT3, but promoted the expression of Cleaved Caspase-3 protein, and enhanced the sensitivity of Tca-8113 cells to 1.668-times of control.Conclusions Interfering EZH2 could promote apoptosis, inhibit proliferation and increase radiosensitivity of squamous cell carcinoma of tongue.
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