| Literature DB >> 30803232 |
Wei Xie, Wei-Wei Deng, Minghui Zan, Lang Rao, Guang-Tao Yu, Dao-Ming Zhu, Wen-Tao Wu, Bei Chen, Li-Wei Ji, Liben Chen1, Kan Liu2,3, Shi-Shang Guo, Hui-Ming Huang, Wen-Feng Zhang, Xingzhong Zhao, Yufeng Yuan4, Wenfei Dong5, Zhi-Jun Sun, Wei Liu4.
Abstract
Although anti-PD-1 immunotherapy is widely used to treat melanoma, its efficacy still has to be improved. In this work, we present a therapeutic method that combines immunotherapy and starvation therapy to achieve better antitumor efficacy. We designed the CMSN-GOx method, in which mesoporous silica nanoparticles (MSN) are loaded with glucose oxidase (GOx) and then encapsulate the surfaces of cancer cell membranes to realize starvation therapy. By functionalizing the MSN's biomimetic surfaces, we can synthesize nanoparticles that can escape the host immune system and homologous target. These attributes enable the nanoparticles to have improved cancer targeting ability and enrichment in tumor tissues. Our synthetic CMSN-GOx complex can ablate tumors and induce dendritic cell maturity to stimulate an antitumor immune response. We performed an in vivo analysis of these nanoparticles and determined that our combined therapy CMSN-GOx plus PD-1 exhibits a better antitumor therapeutic effect than therapies using CMSN-GOx or PD-1 alone. Additionally, we used the positron emission tomography imaging to measuring the level of glucose metabolism in tumor tissues, for which we investigate the effect with the cancer therapy in vivo.Entities:
Keywords: cancer cell membrane; immunotherapy; positron emission tomography; starvation therapy
Year: 2019 PMID: 30803232 DOI: 10.1021/acsnano.8b03788
Source DB: PubMed Journal: ACS Nano ISSN: 1936-0851 Impact factor: 15.881