标题:Targeting blockage of STAT3 inhibits hepatitis B virus-related hepatocellular carcinoma
作者:Yang, Yinli; Zheng, Bingqing; Han, Qiuju; Zhang, Cai; Tian, Zhigang; Zhang, Jian
作者机构:[Yang, Yinli; Zheng, Bingqing; Han, Qiuju; Zhang, Cai; Tian, Zhigang; Zhang, Jian] Shandong Univ, Sch Pharmaceut Sci, Inst Immunopharmaceut Sci, Jinan 更多
通讯作者:Zhang, J
通讯作者地址:[Zhang, J]Shandong Univ, Sch Pharmaceut Sci, Inst Immunopharmaceut Sci, Jinan, Peoples R China.
来源:CANCER BIOLOGY & THERAPY
出版年:2016
卷:17
期:4
页码:449-456
DOI:10.1080/15384047.2016.1156257
关键词:Gene targeted therapy; HBV; HCC; STAT3
摘要:Hepatitis B virus (HBV) infection is a significant cause of liver disease pathogenesis, which results in the development of hepatic dysfunction, cirrhosis and hepatocellular carcinoma (HCC). Our previous studies showed that oncogene STAT3 might be an ideal target for HCC therapy. Here, we investigated whether targeting blockage of STAT3 signaling is efficient for HBV-related HCC. Based on the refractory of HCC and the persistence of HBV, in this study, we designed shRNAs targeting STAT3. The results showed that blocking STAT3 signaling by shRNAs could promote HBV positive HCC cell apoptosis and induce cell cycle arrest, resulting in HCC cell growth inhibition in vitro. Importantly, STAT3-shRNAs efficiently suppressed HBV replication, which would reduce HBV-derived stimulation to STAT3 signaling and augment STAT3-shRNAs-mediated anti-HCC effect. Finally, STAT3-shRNAs-mediated anti-HBV positive HCC effect was confirmed in xenograft nude mice. This study suggested that targeting STAT3 therapies such as STAT3-shRNAs may be an efficacious strategy for HBV-related HCC.
收录类别:SCOPUS;SCIE
WOS核心被引频次:5
Scopus被引频次:7
资源类型:期刊论文
原文链接:https://www.scopus.com/inward/record.uri?eid=2-s2.0-84967203015&doi=10.1080%2f15384047.2016.1156257&partnerID=40&md5=2dbda6da1a35b68fd673061b55544449
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