Mesenchymal stem cells deliver and release conditionally replicative adenovirus depending on hepatic differentiation to eliminate hepatocellular carcinoma cells specifically. Issue 1 (10th October 2016)

• Record Type: Journal Article
• Authors: Yuan, Xiangfei; Zhang, Qing; Li, Zhenzhen; Zhang, Xiaolong; Bao, Shiqi; Fan, Dongmei; Ru, Yongxin; Dong, Shuxu; Zhang, Yizhi; Zhang, Yanjun; Ye, Zhou; Xiong, Dongsheng
• Is Part Of: Cancer letters. Volume 381:Issue 1(2016)
• Page Start: 85
• Page End: 95
• Publication Date: 2016-10-10
• Subjects: CRAd -- microRNA-122 -- AFP promoter -- HUMSC -- Hepatic differentiation -- Hepatocellular carcinoma; Cancer -- Periodicals; Neoplasms -- Periodicals; Cancer -- Périodiques; Electronic journals; 616.994
• DOI: 10.1016/j.canlet.2016.07.019
• Languages: English
• ISSNs: 0304-3835

Abstract

Highlights: This method selectively eliminates hepatoma cells with less damage to liver. The obstacle of adenoviruses intravenous injection is broken by loading them on the HUMSCs. The CRAds are dual regulated by AFP promoter and microRNA-122 target sequence. This targeted method depends on the homing and hepatic differentiation characters of HUMSCs. This method is effective on both orthotopic and subcutaneous xenograft tumor models. Abstract: Currently, it is a key challenge to remove the postsurgical residuals and metastasis of hepatocellular carcinoma (HCC). Oncolytic adenoviral virotherapy is an attractive treatment modality for cancer; however, the difficulty remains regarding its intravenous administration. The aim of this study was to develop a targeted therapeutic system which has great potential to overcome the postsurgical residuals and metastasis of HCC. In this system, we developed a conditionally replicative adenovirus (CRAd) loaded on human umbilical cord-derived mesenchymal stem cells (HUMSCs), in which the CRAd contained an adenovirus E1A gene dual regulated by α-fetoprotein promoter and microRNA-122 target sequence. When HUMSCs homed to the tumor sites and differentiated into hepatocyte-like cells within tumor microenvironment, the CRAds were packaged and released strictly to the local tumor. Subsequently, the CRAd lysed tumor cells selectively with the post-infection regulation. The study showed the specific oncolytic effect of the CRAd to HCC cells and the production of the CRAd by differentiated HUMSCs in vitro . Furthermore, we proved the hepatocyte-like transformation of HUMSC in the microenvironment of orthotopic or heterotopic hepatoma. Finally, this therapeutic system exhibited dramatic tumor inhibition on both orthotopic and subcutaneous hepatic xenograft tumor model mice with less toxicity on normal organs. The study results have demonstrated that this targeted therapeutic strategy is a promising method to resolve the problem of postsurgical residuals and metastasis of HCC.