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Gene expression and antitumor effect following imelectroporation delivery of human interferon α2 gene
引用本文:Zhang GH,Tan XF,Shen D,Zhao SY,Shi YL,Jin CK,Sun WG,Guo YH,Chen KH,Tang J. Gene expression and antitumor effect following imelectroporation delivery of human interferon α2 gene[J]. Acta pharmacologica Sinica, 2003, 24(9): 891-896
作者姓名:Zhang GH  Tan XF  Shen D  Zhao SY  Shi YL  Jin CK  Sun WG  Guo YH  Chen KH  Tang J
摘    要:

关 键 词:肌肉电泳  基因表达  α2干扰素  肿瘤治疗学  白血病  实验研究

Gene expression and antitumor effect following im electroporation delivery of human interferon alpha 2 gene
Zhang Guo-Hua,Tan Xiao-Fan,Shen Dong,Zhao Shu-Yuan,Shi Yan-Li,Jin Cai-Ke,Sun Wei-Gu,Guo Yan-Hong,Chen Kuang-Hueih,Tang Jian. Gene expression and antitumor effect following im electroporation delivery of human interferon alpha 2 gene[J]. Acta pharmacologica Sinica, 2003, 24(9): 891-896
Authors:Zhang Guo-Hua  Tan Xiao-Fan  Shen Dong  Zhao Shu-Yuan  Shi Yan-Li  Jin Cai-Ke  Sun Wei-Gu  Guo Yan-Hong  Chen Kuang-Hueih  Tang Jian
Affiliation:Institute of Cardivascular Basic Research, Peking University Health Science Center, Beijing 100083, China.
Abstract:AIM: To investigate the gene expression and antitumor effect following im electroporation delivery of human interferon alpha 2 (hIFN-alpha 2) gene. METHODS: The pcD2/hIFN-alpha 2 was injected into the middle of the quadriceps muscle of female BALB/c mice or the leukemia-bearing female BALB/c nude mice, and then electroporation was given to the injection site. Optimal electrical parameters and the efficiency of gene transfer was studied with hIFN-alpha 2 ELISA kit. The HL-60 tumor model in BALB/c nude mice was used to investigate therapeutic effects of im electroporation delivery of pcD2/hIFN-alpha 2. RESULTS: The optimal conditions for the electric pulses were as follows: voltage at 200 V/cm; pulse duration at 40 ms per pulse; number of pulse at 6 pulses and frequency at 1 Hz. Under optimal conditions, the serum hIFN-alpha 2 levels in electroporation group (160 microg/L+/-31 microg/L) were 45-fold higher than those of nonelectroporation group (3.6 microg/L+/-1.6 microg/L, P<0.01). The growth of leukemia was inhibited more obviously and the survival time of the leukemia-bearing nude mice was prolonged after im electroporation delivery of pcD2/hIFN-alpha 2 100 microg or 200 microg. CONCLUSION: Electroporation was an efficient method for the delivery of plasmid DNA and im electroporation delivery of pcD2/hIFN-alpha 2 was effective in treating leukemia.
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