The present invention is VEGF-A, VEGF-B, and VEGF-C antisense cDNA containing a rAAV vector and VEGF receptor protein (VEGFR) of the truncated soluble cDNA containing a rAAV vector containing the arm of a gene therapy to about it. ; Gene therapy according to the present invention can be used effectively in the treatment of cancer by inhibiting the expression of VEGF and functions involved in angiogenesis is essential for the proliferation and metastasis, by reducing the growth of tumors in the gene level. ; rAAV, gene therapy, VEGF, VEGF receptor, adeno-associated virus
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