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华蟾素对喉癌细胞株的诱导分化研究
引用本文:韩仲明,苏红星,张敏燕,孙宝春,张海荣,黄晋生. 华蟾素对喉癌细胞株的诱导分化研究[J]. 中国中西医结合耳鼻咽喉科杂志, 2004, 12(5): 241-243
作者姓名:韩仲明  苏红星  张敏燕  孙宝春  张海荣  黄晋生
作者单位:1. 北京第二炮兵总医院耳鼻咽喉科,100088
2. 首都医科大学基础医学院组织胚胎教研组
3. 海军总医院中心实验室
摘    要:目的研究华蟾素(Cinobutacini,CIN)对喉癌细胞的诱导分化作用.方法体外培养喉癌细胞(Hep-2)放射性同位素掺入法检测CIN对Hep-2的生长抑制作用,原位杂交方法检测c-myc(细胞核内癌基因)的表达变化.结果CIN低浓度在24小时内有促进Hep-2细胞分裂、增殖并诱导细胞分化作用;高浓度作用72小时则抑制Hep-2细胞生长.3H-脱氧胸苷(3H-TdR)掺入量检测提示,CIN短时间作用的Hep-2细胞cpm(每分钟脉冲数)值增高,而长时间作用组则cpm值下降.CIN作用48小时后,Hep-2细胞内c-myc蛋白表达较对照组低,但较平阳霉素组高.结论中药华蟾素在低浓度和时间相对较短时对人喉癌Hep-2细胞具有诱导分化作用,当作用时间超过72小时,则表现为抑制肿瘤细胞生长作用.

关 键 词:华蟾素  分化诱导  喉瘤细胞株
修稿时间:2003-03-31

The differentiation-inducing effect of cinobutacini on human laryngeal carcinoma cell line Hep-2
HAN Zhongming,SU Hongxing,ZHANG Minyan,SUN Baochun,ZHANG Hairong,HUANG Jinsheng Dept. of Otolaryngology,the General Hospital of PLA nd Artillery,Beijing. The differentiation-inducing effect of cinobutacini on human laryngeal carcinoma cell line Hep-2[J]. Chinese Journal of Otorhinolaryngology of Integrated Traditional and Western Medicine, 2004, 12(5): 241-243
Authors:HAN Zhongming  SU Hongxing  ZHANG Minyan  SUN Baochun  ZHANG Hairong  HUANG Jinsheng Dept. of Otolaryngology  the General Hospital of PLA nd Artillery  Beijing
Affiliation:HAN Zhongming,SU Hongxing,ZHANG Minyan,SUN Baochun,ZHANG Hairong,HUANG Jinsheng Dept. of Otolaryngology,the General Hospital of PLA 2nd Artillery,Beijing 100088
Abstract:Objective To investigate the differentiation-inducing effect of cinobutacini (CIN)on human laryngeal carcinoma cell line Hep-2. Methods Radioisotope 3H labeled TdR (3H-TdR) was used to determine the growth-inhibiting effect of CIN on Hep-2 by the incorporation method and in situ hybridization technique was taken to detect the changes in the expressive level of oncogene c-myc in these cells, with the morphological changes observed microscopically on the cultured cells in vitro. Results CIN could cause Hep-2 cells dividing to show a tendency of proliferating and a differentiation-inducing effect on the cells cultured together with it for 24 hours at lower concentration,while it showed an inhibitory effect on Hep 2 cultured together for 72 hours at higher concentration. These effects were shown as the content changes of 3H-TdR incorporated to the nucleus of Hep-2 cells. Moreover,the expressive level of c myc protein was significantly lower in the cells cultured together with CIN for 48 hours,than that in the controls, while it was higher than that in the cells cultured with pingyangmyinycin. Conclusions CIN can bring about differentiation-inducing effect on Hep-2 when cultured together with it at lower concentration for a shorter period of time. However, it causes an inhibitory effect on these cells when cultured together for more than 72h.
Keywords:Cinobutacini  Differentiation-inducing  Laryngeal carcinoma cell line
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