Author/Authors :
Jiang، نويسنده , , Tao and Zhou، نويسنده , , Changdong and Gu، نويسنده , , Junlian and Liu، نويسنده , , Yanan and Zhao، نويسنده , , Lijing and Li، نويسنده , , Wei and Wang، نويسنده , , Guanjun and Li، نويسنده , , Yang and Cai، نويسنده , , Lu، نويسنده ,
Abstract :
Prostate cancer urgently needs an efficient therapy. Here we demonstrated that cisplatin combined with gene therapy by transfecting the attenuated Salmonella that carry a plasmid containing p53 gene and MDM2 siRNA provided a super-synergistic effect on the inhibition of prostate cancer growth in vivo. This synergistic therapy was associated with the induction of apoptotic cell death with a decreased Bcl2 to Bax expression ratio and increased expression of cleaved caspase 3 and caspase 9 in the prostate cancer xenograft. These results indicate that cisplatin-chemotherapy in combination with targeting the MDM2/p53 axis is an attractive strategy to treat prostate cancer.
Keywords :
p53 , prostate cancer , apoptosis , Cisplatin (DDP) , Xenograft mice model , Si RNA-mdm2