Construction of Aptamer-siRNA Chimera/PEI/5-FU/Carbon Nanotube/Collagen Membranes for the Treatment of Peritoneal Dissemination of Drug-Resistant Gastric Cancer

被引:29
作者
Chen, Wen [1 ]
Yang, Sainan [2 ]
Wei, Xia [2 ]
Yang, Zailin [2 ]
Liu, Dongxu [1 ]
Pu, Xin [2 ]
He, Silian [2 ]
Zhang, Yong [2 ]
机构
[1] Chinese Peoples Liberat Army Gen Hosp, Dept Pathol, Med Ctr 8, Beijing 100091, Peoples R China
[2] Chongqing Med Univ, Affiliated Hosp 3, Dept Hematol, Gener Hosp, Chongqing 401120, Peoples R China
基金
中国国家自然科学基金;
关键词
aptamers; carbon nanotubes; gastric cancer; peritoneal dissemination; siRNA; EXPRESSION;
D O I
10.1002/adhm.202001153
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Due to extensive metastasis, poor blood supply, and drug-resistant, there is still no effective clinical means to treat peritoneal dissemination of gastric cancer. Here, an aptamer-siRNA chimera (Chim)/polyethyleneimine (PEI)/5-fluorouracil (5-FU)/carbon nanotube (CNT)/collagen membrane is constructed, which could be divided into 15 layers with a thickness of 70-100 mu m. Sustained release experiments show that the collagen membranes can control 5-FU release for more than 2 weeks. Aptamer-siRNA chimera can specifically bind to gastric cancer cells, enabling targeted delivery of 5-FU and silencing drug-resistant gene. In vitro experiments demonstrated that Chim/PEI/5-FU/CNT nanoparticles promoted the apoptosis of 5-FU-resistant gastric cancer cells, inhibited their invasion and proliferation. Animal experiments show that Chim/PEI/5-FU/CNT/collagen membrane significantly inhibits the expression of mitogen-activated protein kinase (MAPK), and effectively treats peritoneal dissemination of 5-FU-resistant gastric cancer. Compared with siRNA/PEI/5-FU/CNT group, ki-67 proliferation index, and matrix metallopeptidase 9 (MMP9) expression are significantly decreased in the Chim/PEI/5-FU/CNT group, while the proportion of apoptotic cells is markly increased. In conclusion, a chimera/PEI/5-FU/CNT/collagen membrane is constructed, which can effectively treat peritoneal dissemination of drug-resistant gastric cancer. The study provides a new therapeutic approach for relevant clinical treatment.
引用
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页数:8
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