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重组腺病毒介导的FLT3配体和阿霉素联合治疗小鼠肝癌
引用本文:李刚,卫立辛,杨庆,贾凤岐,张柏和,吴孟超. 重组腺病毒介导的FLT3配体和阿霉素联合治疗小鼠肝癌[J]. 第二军医大学学报, 2003, 24(4): 390-392
作者姓名:李刚  卫立辛  杨庆  贾凤岐  张柏和  吴孟超
作者单位:1. 第二军医大学长海医院普通外科,上海,200433
2. 东方肝胆外科医院,上海,200438
基金项目:国家自然科学基金(39730440).
摘    要:目的:将重组腺病毒介导的FLT3配体(FLT3 ligand,FL)与阿霉素(adriamycin,ADM)联合治疗小鼠肝癌,探索基因治疗和化疗相结合治疗肿瘤的新方法。方法:构建携带鼠FL的重组腺病毒载体(AdmFL),单独用其或ADM以及两者联用对实验性肝癌小鼠进行治疗,观察抗肿瘤效果。结果:(1)FL+ADM组小鼠肝癌生长抑制率最大值为56.5%,明显高于ADM组和FL组的27.5%和26.6%(P<0.01);(2)FL+ADM组小鼠早期死亡率为8.3%,明显低于ADM组的37.5%(P<0.01);FL十ADM组小鼠长期生存率为86.4%,明显高于ADM组和FL组的50.0%和41.5%(P<0.01)。结论:(1)FL和ADM治疗小鼠肝癌具有协同作用,FL可显著增强化疗效果;(2)FL能明显降低化疗不良反应。

关 键 词:重组腺病毒介导 FLT3配体 阿霉素 联合治疗 小鼠 肝癌
文章编号:0258-879X(2003)04-0390-03
修稿时间:2002-08-10

Treatment of hepatoma in mice by adenovirus-mediated FLT3-ligand combined with adriamycin
LI Gang,WEI Li-Xin,YANG Qing,JIA Feng-Qi,ZHANG Bai-He,WU Meng-Chao. Treatment of hepatoma in mice by adenovirus-mediated FLT3-ligand combined with adriamycin[J]. Former Academic Journal of Second Military Medical University, 2003, 24(4): 390-392
Authors:LI Gang  WEI Li-Xin  YANG Qing  JIA Feng-Qi  ZHANG Bai-He  WU Meng-Chao
Abstract:Objective: To study the effects of adenovirus-mediated FLT3-ligand and/or adriamycin(ADM) on hepatoma in mice and to explore a new way for hepatoma gene therapy combined with chemotherapy. Methods: The recombinant aden-ovirus vector carrying murine FLT3 ligand (AdmFL) was constructed, AdmFL and/or ADM were injected into the tumor-bearing mice. Their effects on the growth of the tumor and the survival rate of the mice were observed. Results: (1)In FL + ADM group,the hepatoma cell suppression percentage was 56. 5% , while the percentage in ADM group and FL group were 27. 5% and 26. 6%(F<0. 01) respectively; (2) In FL + ADM group,the early death rate was 8. 3%,while the rate in ADM group was 37. 5% ; in FL + ADM group,the survival percentage of mice was 86. 4% , while the percentage in ADM group and FL group were 50% and 41. 5%(P<0. 01) respectively. Conclusion: FL can significantly enhance the effeciency of ADM chemotherapy, and relieve the toxic effects of ADM chemotherapy.
Keywords:FLT3 ligand  adenovirus  adriamycin  liver neoplasms  experimental  gene therapy  drug therapy
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