杨卫忠, 陈春美, 石松生, 王春华, 杨贤义, 王锐. 榄香烯抑制人脑胶质瘤U251细胞株c-myc癌基因表达及其影响细胞凋亡机制的研究[J]. 中国肿瘤临床, 2005, 32(13): 763-766.
引用本文: 杨卫忠, 陈春美, 石松生, 王春华, 杨贤义, 王锐. 榄香烯抑制人脑胶质瘤U251细胞株c-myc癌基因表达及其影响细胞凋亡机制的研究[J]. 中国肿瘤临床, 2005, 32(13): 763-766.
Yang Wei-zhong, Chen Chun-mei, Shi Song-sheng, . The Study on Inhibition of the Expression of c-myc Gene of Human Glioma U251 Cell Line and the Effect Mechanism of Effect on Cellular Apoptosis by Elemene[J]. CHINESE JOURNAL OF CLINICAL ONCOLOGY, 2005, 32(13): 763-766.
Citation: Yang Wei-zhong, Chen Chun-mei, Shi Song-sheng, . The Study on Inhibition of the Expression of c-myc Gene of Human Glioma U251 Cell Line and the Effect Mechanism of Effect on Cellular Apoptosis by Elemene[J]. CHINESE JOURNAL OF CLINICAL ONCOLOGY, 2005, 32(13): 763-766.

榄香烯抑制人脑胶质瘤U251细胞株c-myc癌基因表达及其影响细胞凋亡机制的研究

The Study on Inhibition of the Expression of c-myc Gene of Human Glioma U251 Cell Line and the Effect Mechanism of Effect on Cellular Apoptosis by Elemene

  • 摘要: 目的: 探讨榄香烯对人脑胶质瘤U251细胞株c-myc癌基因表达及其影响细胞凋亡的机制。 方法: 应用榄香烯处理人脑胶质瘤U251细胞株,应用MTT法检测细胞增殖抑制试验,并求出半数致死浓度(IC50),倒置显微镜和电镜观察经榄香烯处理的U251细胞形态,流式细胞仪检测细胞周期的变化,凝胶电泳检测凋亡梯度,免疫荧光技术观察凋亡小体,免疫组织化学检测c-myc蛋白和RT-PCR检测c-myc基因的表达。 结果: 榄香烯对U251细胞株增殖具有抑制作用,呈剂量和作用时间的依赖性,IC50为0.062mg/ml,倒置显微镜下可见榄香烯组细胞皱缩、变小,电镜下可见具有典型新月形核的凋亡细胞和凋亡小体,流式细胞仪检测榄香烯阻滞U251细胞株周期中S期向G2/M期的转变过程,减少有丝分裂,并引起细胞凋亡,琼脂糖凝胶电泳获得清晰的凋亡特征性梯形条带,免疫荧光技术观察凋亡小体,免疫组织化学和RT-PCR分别证实榄香烯抑制c-myc蛋白和c-myc基因的表达。 结论: 榄香烯可抑制人脑胶质瘤U251细胞株c-myc癌基因表达,并通过下调U251细胞株的凋亡途径,促进肿瘤细胞凋亡,抑制细胞增殖。

     

    Abstract: Objective : To investigate the inhibition of the expression of c-myc gene of human glioma U251 cell line and the mechanism of effect on cellular apoptosis by the elemene. Methods : We studied on the two groups: the normal controls and the treatment groups with elemene in human glioma U251, then examined the inhibition test by MTT methods and worked out the IC50, watched the morphological alterations by inverted microscope and electron microscope, evaluated the apoptosis by flow cytometry analysis, agarose gel electrophoresis and light microscopy, and examined the expression of c-myc protein and gene by immunohistochemical method and RT-PCR. Results : Our studies showed that elemene had a markedly antineoplastic activity on glioma U251 cell line with the dependence of dose and time, IC50 was 0.062 mg/ml. After administration of elemene the cellular morphology became small under inverted microscopy and found apoptotic cell and bodies under electron microscope.The flow cytometry analysis showed that elemene inhibited the cell cycle transference from phaseS to phase T2/M and induced the apoptosis. The apoptosis in glioma cells was confirmed by DNA ladder formation on gel electrophoresis. Our studies showed that elemene inhibited the expression of c-myc protein and gene by immunohistochemical method and RT-PCR. Conclusion : Elemene inhibits the expression of c-myc gene, induce apoptosis and has a marked antiproliferative effect on glioma cells.

     

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