Efficient targeted tumor imaging and secreted endostatin gene delivery by anti-CD105 immunoliposomes

• Published in: Journal of experimental & clinical cancer research 2018-03, Vol.37 (1), p.42-42, Article 42
• Main Authors: Zhuo, Huiqin, Zheng, Baoshi, Liu, Jianming, Huang, Yong, Wang, Huiling, Zheng, Duo, Mao, Naiquan, Meng, Jinyu, Zhou, Sufang, Zhong, Liping, Zhao, Yongxiang
• Format: Article
• Language: English
• Subjects: Animals; Anti-CD105 immunoliposome; Antibodies, Monoclonal - administration & dosage; Cancer; Care and treatment; Cell Line, Tumor; Chromatography, High Pressure Liquid; Disease Models, Animal; Endoglin - antagonists & inhibitors; Endostatins - biosynthesis; Endostatins - genetics; Female; Gene therapy; Gene Transfer Techniques; Genetic Therapy; Glutathione - metabolism; Humans; In vivo imaging; Liposomes; Liposomes - chemistry; Liposomes - ultrastructure; Methods; Mice; Molecular Imaging; Neoplasms - diagnosis; Neoplasms - genetics; Neoplasms - therapy; Optical Imaging - methods; Physiological aspects; Plasmids - chemistry; Plasmids - genetics; Secreted endostatin; Superoxide Dismutase - metabolism; Tandem Mass Spectrometry; Transgenes; Tumor vascular targeting
• ISSN: 1756-9966; 0392-9078; 1756-9966
• DOI: 10.1186/s13046-018-0712-8

Anti-CD105 mAb-conjugated immunoliposomes, loaded with secreted mouse endostatin gene, were developed for targeted tumor imaging and antiangiogenic gene therapy. The liposomes were investigated for size, zeta-potential, lipid content, antibody binding ability, and pcDNA loading capacity. The ability of immunoliposomes to target tumor-derived endothelial cells and perform gene transfer in vitro was measured and their basic biocompatibility was evaluated. A nude mouse/breast cancer xenograft model was used to examine the tumor internalization of fluorescent-labeled liposomes and the clinical potential of immnuoliposomes loaded with pcDNA3.1-CSF1-endostatin. Loaded immunoliposomes were homogenously distributed with a well-defined spherical shape and bilayer, diameter of 122 ± 11 nm, and zeta potential + 1.40 mV. No significant differences were observed in body weight, liver index, oxidative stress, or liver and kidney function in mice after liposomes exposure. The addition of CD105 mAb to liposomes conferred the ability to target tumor-derived endothelial cells in vitro and in vivo. Systemic intravenous administration of fluorescent immunoliposomes in the xenograft model resulted in selective and efficient internalization in tumor vasculature. Treatment of mice with pcDNA3.1-CSF1-endostatin-loaded immunoliposomes suppressed tumor growth by 71%. These data demonstrate the advantages of using anti-CD105 mAb-conjugated immunoliposomes to enhance tumor targeting, imaging, and gene transfer applications.