• Department of General Surgery, First Affiliated Hospital, West China University of Medical Sciences, Chengdu 610041;
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Objective  To explore the feasibility of recombinant adeno-associated virus (rAAV) as a vector for the gene therapy of liver cancer.
Methods  The rAAV/enhance green fluorescein protein (EGFP) recombinant was prepared by the routine method of two plasmids cotransfection.
Results  The experiment showed that one 10cm plate could produce 107-108 infection unit recombinant by the method of two plasmids cotransfection, and the transduction of HepG2 cell was increased with the increase of infection dosage of rAAV. About 100 multiplicity of infection (MOI) AAV vector could make all the tumor cell light. Conclusion  Liver cancer cell can be efficiently transduced by rAAV, and AAV vector may be a valuable vector for the gene therapy of liver cancer.

Citation: LIU Ziming,YAN Lnan,WANG Zhong,et al.. THE RESEARCH ON THE RECOMBINANT ADENO-ASSOCIATED VIRUS AS A VECTOR FOR THE GENE THERAPY OF LIVER CANCER. CHINESE JOURNAL OF BASES AND CLINICS IN GENERAL SURGERY, 2001, 8(3): 133-134. doi: Copy