ZHAO Jing-guo,NI Yan-jun,SUN Ting.Anti-tumor effects of Egr-IFNγ gene therapy combined with 125I -UdR radionuclide therapy[J].Chinese Journal of Radiological Medicine and Protection,2008,28(6):606-608
Anti-tumor effects of Egr-IFNγ gene therapy combined with 125I -UdR radionuclide therapy
Received:November 29, 2007  
DOI:
KeyWords:IFNγ  H22 cells  Gene-radiotherapy  Deoxyuridine  Iodine radioisotopes
FundProject:国家自然科学基金资助项目(30600160)
Author NameAffiliationE-mail
ZHAO Jing-guo No.403 Hosptial of PLA, Dalian 116015, China  
NI Yan-jun 沈阳军区总医院  
SUN Ting 吉林大学基础医学院生物化学教研室  
宋享福 吉林大学公共卫生学院  
马庆杰 吉林大学中日联谊医院  
李修义 吉林大学公共卫生学院  
高凤彤 吉林大学中日联谊医院  
杨巍 苏州大学放射医学与公共卫生学院放射生物教研室 detachedy@yahoo.com.cn 
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Abstract::
      Objective To explore the anti-tumor effects of Egr-IFNγ gene therapy combined with 125I-UdR radionuclide therapy in mice bearing H22 hepatocarcinoma and its mechanism.Methods The recombinant plasmid pcDNAEgr-IFNγ mixed with liposome was injected into tumor. 48 h later, 370 kBq 125I-UdR was injected into tumor. The tumor growth rates at different times were observed. After 3 d gene-radionuclide therapy, the concentration of IFNγ in cytoplasm of H22 cells and cytotoxic activities of splenic CTL of the mice in different groups were examined. Results The tumor growth rates of pcDNAEgr-IFNγ+ 125I -UdR group were obviously lower than those of control group, 125I -UdR group and pcDNAEgr-1+125I-UdR group 6-15d after gene-radionuclide therapy. IFNγ protein was found in cytoplasm of H22 cells in pcDNAEgr-IFNγ+125I-UdR group after 3 d gene-radionuclide therapy. Cytotoxic activity of splenic CTL in pcDNAEgr-IFNγ+125I-UdR group was significantly higher than that in the other groups (P<0.01). Conclusions The anti-tumor effects in vivo of pcDNAEgr-IFNγ gene therapy combined with 125I -UdR radionuclide therapy are better than those of 125I -UdR therapy.
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