Oncolytic virus carrying shRNA targeting SATB1 inhibits prostate cancer growth and metastasis

被引:20
|
作者
Mao, Li-jun [1 ,2 ]
Zhang, Jie [2 ]
Liu, Ning [2 ]
Fan, Li [2 ]
Yang, Dong-rong [1 ]
Xue, Bo-xin [1 ]
Shan, Yu-xi [1 ]
Zheng, Jun-nian [2 ]
机构
[1] Soochow Univ, Affiliated Hosp 2, Dept Urinary Surg, Suzhou 215004, Peoples R China
[2] Xuzhou Med Coll, Jiangsu Key Lab Biol Canc Therapy, Xuzhou 221002, Peoples R China
基金
中国国家自然科学基金;
关键词
Oncolytic adenovirus; SATB1; Prostate cancer; shRNA; POTENT ANTITUMORAL EFFICACY; SILENCING SATB1; DRUG-RESISTANCE; TUMOR-GROWTH; CELL-GROWTH; PROLIFERATION; VIROTHERAPY; INVASION;
D O I
10.1007/s13277-015-3658-x
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Recent studies suggest that SATB1 is a promising therapeutic target for prostate cancer. To develop novel SATB1-based therapeutic agents for prostate cancer, in this study, we aimed to construct ZD55-SATB1, an oncolytic adenovirus ZD55 carrying shRNA targeting SATB1, and investigate its effects on the inhibition of prostate cancer growth and metastasis. ZD55-SATB1 was constructed and used to infect human prostate cancer cell lines DU145 and LNCaP. The inhibitory effect of ZD55-SATB1 on SATB1 expression was evaluated by reverse transcription polymerase chain reaction (RT-PCR) and Western blot analysis. The cytotoxicity of ZD55-SATB1 was detected by MTT assay. Cell invasion was detected by Matrigel invasion assay. The in vivo antitumor activities of ZD55-SATB1 were evaluated in xenograft mouse model. We found that ZD55-SATB1 selectively replicated and significantly reduced SATB1 expression in DU145 and LNCaP cells. ZD55-SATB1 effectively inhibited the viability and invasion of DU145 and LNCaP cells in vitro and inhibited prostate cancer growth and metastasis in xenograft nude mice. In conclusion, replicative oncolytic adenovirus armed with SATB1 shRNA exhibits effective antitumor effect in human prostate cancer. Our study provides the basis for the development of ZD55-SATB1 for the treatment of prostate cancer.
引用
收藏
页码:9073 / 9081
页数:9
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