Oncolytic Adenovirus with SPAG9 shRNA Driven by DD3 Promoter Improved the Efficacy of Docetaxil for Prostate Cancer

被引:0
|
作者
Lu, Meng [1 ,2 ]
Wei, Fu-kun [2 ]
Wu, Chuang [2 ]
Xu, Zi-yang [2 ]
Mao, Li-jun [2 ]
Yang, Dong-rong [1 ]
机构
[1] Soochow Univ, Dept Urol, Affiliated Hosp 2, Suzhou 215004, Jiangsu, Peoples R China
[2] Xuzhou Med Univ, Dept Urol, Affiliated Hosp, Xuzhou 221002, Jiangsu, Peoples R China
基金
中国国家自然科学基金;
关键词
PROLIFERATION; CELLS; CHEMOTHERAPY; EXPRESSION; APOPTOSIS; DD3(PCA3); INVASION; TARGETS; GROWTH; EMT;
D O I
10.1155/2022/7918067
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Prostate cancer (PCa) is a common malignant tumor of the male urinary system and ranks the second in the causes of tumor-related deaths. Differential display code 3 (DD3) is a noncoding gene that is specifically expressed in PCa. High expression of sperm-associated antigen 9 (SPAG9) is closely related to tumorigenesis of PCa, and SPAG9 is a therapeutic target for PCa. In this study, a new oncolytic adenovirus DD3-ZD55-SPAG9 was constructed by using DD3 promoter to enhance the efficacy and safety of adenovirus. The combined use of DD3-ZD55-SPAG9 and docetaxel showed that DD3-ZD55-SPAG9 significantly improved the anti-tumor efficacy of docetaxel in PCa both in vitro and in vivo. The mechanism was related to the induction of tumor cell apoptosis and the inhibition of tumor cell invasion. In conclusion, DD3-ZD55-SPAG9 combined with docetaxel is an effective strategy for PCa therapy.
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页数:10
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