Enhanced growth inhibition of prostate cancer in vitro and in vivo by a recombinant adenovirus-mediated dual-aptamer modified drug delivery system
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Successfully established a dual aptamer modified tumor targeting gene and DOX delivery system mediated by recombinant adenovirus.

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The uptake of ADDP-Ad5 and expression of reporter gene are enhanced by the system in LNCaP and PC3 cells.

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ADDP-Ad5 significantly inhibits the cell growth of LNCaP and PC3 cells but not WPMY-1 cells.

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ADDP-Ad5 is active in vivo against LNCaP and PC3 tumor xenografts and has no or slight toxicity to the mice.

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