| Literature DB >> 26897539 |
Xibo Ma1, Hui Hui2, Yushen Jin3, Di Dong2, Xiaolong Liang4, Xin Yang2, Ke Tan5, Zhifei Dai4, Zhen Cheng6, Jie Tian7.
Abstract
SM5-1 is a humanized mouse monoclonal antibody, targeting an over-expressed membrane protein of approximately 230 kDa in hepatocellular carcinoma (HCC). SM5-1 can be used for target therapy in hepatocellular carinoma due to its ability of inhibiting cell growth and inducing apoptosis. However, the tumor inhibition efficacy of SM5-1 in HCC cancer treatment remains low. In this study, we synthesized SM5-1-conjugated gold nanoparticles (Au-SM5-1 NPs) and investigated their anticancer efficacy in HCC both in vitro and in vivo. The tumor inhibition rates of Au-SM5-1 NPs for subcutaneous tumor mice were 40.10% ± 4.34%, 31.37% ± 5.12%, and 30.63% ± 4.87% on day 12, 18, and 24 post-treatment as determined by bioluminescent intensity. In addition, we investigated the antitumor efficacy of Au-SM5-1 NPs in orthotopic HCC tumor models. The results showed that the inhibition rates of Au-SM5-1 NPs can reach up to 39.64% ± 4.87% on day 31 post-treatment determined by the bioluminescent intensity of the abdomen in tumor-bearing mice. Furthermore, three-dimensional reconstruction results of the orthotopic tumor revealed that Au-SM5-1 NPs significantly inhibited tumor growth compared with SM5-1 alone. Our results suggested that the developed Au-SM5-1 NPs has great potential as an antibody-based nano-drug for HCC therapy.Entities:
Keywords: Antibody therapy; Bioluminescence tomography; Cell proliferation; Gold nanoparticles; Hepatocellular carcinoma
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Year: 2016 PMID: 26897539 DOI: 10.1016/j.biomaterials.2016.02.007
Source DB: PubMed Journal: Biomaterials ISSN: 0142-9612 Impact factor: 12.479