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Suicide gene therapy of hepatocellular carcinoma and delivery procedure and route of therapeutic gene in vivo

Suicide gene therapy of hepatocellular carcinoma and delivery procedure and route of therapeutic gene in vivo

作     者:Sun X.-Y. Wu Z.-D. Hu J.-B. 

作者机构:Department of Surgery Tongji Hospital Tongji Med. Coll. Huazhong Univ. Sci Wuhan 430030 China 

出 版 物:《Hepatobiliary & Pancreatic Diseases International》 (国际肝胆胰疾病杂志(英文版))

年 卷 期:2002年第1卷第3期

页      面:373-377页

学科分类:1002[医学-临床医学] 100214[医学-肿瘤学] 10[医学] 

主  题:hepatocellular carcinoma gene therapy gene transfer in vivo tk gene bystander effect Epstein-Barr virus 

摘      要:Objective: To study the induction of sensitivity toganciclovir (GCV) or acyclovir (ACV) in humanhepatocellular carcinoma (HCC) cell line trans-ferred by an Epstein-Barr virus (EBV)-based repli-con expression vector carrying the herpes simplex vi-rus thymidine kinase (HSV-tk) gene, including kill-ing and bystander effect, and also the gene delive-ry procedure and route of gene therapy in vivo ***: Liposome-entrapped plasmid pDR2/tk wastransferred into HCC cells, and then different con-centrations of GCV or ACV were added. The trans-ferred cells were mixed with untransferred HCC cellsin different proportion and 200 μmol/L GCV wasthen added into each well. After 72 hours, all sam-ples were measured by MTT colorimetric assay. AnEBV-based plasmid eukarotic expression vector car-rying IL-2 cDNA was used. Three models of gene di-rect injection in the local liver, injection through theportal vein, and injection through the embolized he-patic artery were established in closed Wister *** each model, two subgroups, injected either na-ked plasmid DNA or lipofectin-plasmid complex wereincluded. The expression of the IL-2 gene was regu-larly examined ***: GCV or ACV could apparently kill thetransferred HCC cells at a concentration of 0. 2μmol/L. The inhibition rate was changed with dif-ferent drug concentrations. The bystander effectwas obviously induced at a transferred to untrans-ferred HCC cells ratio of 1:5. IL-2 gene expressionwas observed in liver cells of all animals on day 3,which reached peak within 3-7 days, and declined af-ter day 7. Injection of naked plasmid DNA throughthe hepatic artery plus embolization obtained a ***: EBV-based vector is suitable for carry-ing suicide gene therapy for hepatocellular carcino-ma. Gene direct delivery in vivo combined with in-terventional surgery can be used to treat hepatocellu-lar carcinoma.

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