Efficient miRNA Inhibitor Delivery with Graphene Oxide-Polyethylenimine to Inhibit Oral Squamous Cell Carcinoma

被引:34
作者
Ou, Lingling [1 ]
Sun, Ting [1 ]
Liu, Minyi [1 ]
Zhang, Ye [1 ]
Zhou, Zhiying [1 ]
Zhan, Xiaozhen [1 ]
Lu, Lihong [1 ]
Zhao, Qingtong [1 ]
Lai, Renfa [1 ]
Shao, Longquan [2 ]
机构
[1] Jinan Univ, Affiliated Hosp 1, Dept Stomatol, Guangzhou 510632, Peoples R China
[2] Southern Med Univ, Stomatol Hosp, Dept Prosthodont, Guangzhou 510260, Peoples R China
基金
中国国家自然科学基金;
关键词
oral squamous cell carcinoma; GO-PEI; miR-214; inhibitor; gene therapy; IN-VIVO; GENE DELIVERY; FUNCTIONALIZED GRAPHENE; PROGNOSTIC VALUE; DRUG-DELIVERY; NANO-GRAPHENE; CANCER CELLS; E-CADHERIN; EXPRESSION; MICRORNAS;
D O I
10.2147/IJN.S220057
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Background: MicroRNAs (miRNAs) are widely believed to be promising targets for oral squamous cell carcinoma (OSCC) gene therapy. miR-214 has been identified as a promoter of OSCC aggression and metastasis. Methods: Graphene oxide-polyethylenimine (GO-PEI) complexes were prepared and loaded with a miRNA inhibitor at different N/P ratios. The transfection efficiency of GO-PEI-inhibitor was tested in Cal27 and SCC9 cells. Moreover, the tumor inhibition ability of GO-PEI-inhibitor was measured in an OSCC xenograft mouse model by intratumoral injection. Results: Here, we show that a GO-PEI complex efficiently delivers a miR-214 inhibitor into OSCC cells and controls the intracellular release of the miR-214 inhibitor. These results indicate that the GO-PEI-miR-214 inhibitor complex efficiently inhibited cellular miR-214, resulting in a decrease in OSCC cell invasion and migration and an increase in cell apoptosis by targeting PTEN and p53. In the xenograft mouse model, the GO-PEI-miR-214 inhibitor complex significantly prevented tumor volume growth. Conclusion: This study indicates that functionalized GO-PEI with low toxicity has promising potential for miRNA delivery for the treatment of OSCC.
引用
收藏
页码:1569 / 1583
页数:15
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