Gold Nanoparticle-Mediated Targeted Delivery of Recombinant Human Endostatin Normalizes Tumour Vasculature and Improves Cancer Therapy

被引:102
作者
Li, Wei [1 ]
Zhao, Xiaoxu [1 ]
Du, Bin [2 ]
Li, Xin [1 ]
Liu, Shuhao [1 ]
Yang, Xiao-Yan [1 ]
Ding, Hui [1 ]
Yang, Wende [1 ]
Pan, Fan [1 ]
Wu, Xiaobo [1 ]
Qin, Li [3 ]
Pan, Yunlong [1 ]
机构
[1] Jinan Univ, Affiliated Hosp 1, Dept Gen Surg, Guangzhou 510632, Guangdong, Peoples R China
[2] Jinan Univ, Affiliated Hosp 1, Dept Pathol, Guangzhou 510632, Guangdong, Peoples R China
[3] Jinan Univ, Sch Med, Dept Histol & Embryol, Guangzhou 510632, Guangdong, Peoples R China
来源
SCIENTIFIC REPORTS | 2016年 / 6卷
基金
中国国家自然科学基金;
关键词
ANGIOGENESIS; VEGF; METASTASIS; LYMPHANGIOGENESIS; MICROENVIRONMENT; BIODISTRIBUTION; INHIBITOR; PERICYTES; PATHWAYS; CELLS;
D O I
10.1038/srep30619
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Tumour vasculature is generally disordered because of the production of excessive angiogenic factors by tumour cells, which results in tumour progression and reduces the effectiveness of radiotherapy or chemotherapy. Transient anti-angiogenic therapies that regulate tumour vascular morphology and function and improve the efficiency of antitumour therapy are under investigation. Recombinant human endostatin (Endostar/rhES) is a vascular angiogenesis-disrupting agent that has been used to treat non-small cell lung cancer (NSCLC) in the clinical setting. In this study, we used gold nanoparticles (AuNPs) as a drug-delivery system (DDS) for targeted tumour delivery of rhES for short therapy, which resulted in transient tumour vascular normalization, reduced permeability and hypoxia, strengthened blood vessel integrity, and increased blood-flow perfusion. Moreover, combination therapy with 5-FU over this timeframe was substantially more effective than 5-FU monotherapy. In conclusion, our research demonstrates the potential use of AuNPs as a drug-delivery platform for transporting rhES into a tumour to induce transient tumour vascular normalization and enhance the antitumour efficacy of cytotoxic drugs.
引用
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页数:11
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