Gold nanoparticles delivered miR-375 for treatment of hepatocellular carcinoma

被引:45
|
作者
Xue, Hui-Ying [1 ,2 ]
Liu, Yong [1 ,2 ]
Liao, Jia-Zhi [1 ]
Lin, Ju-Sheng [1 ]
Li, Bin [2 ]
Yuan, Wei-Gang [2 ]
Lee, Robert J. [3 ]
Li, Lei [2 ]
Xu, Chuan-Rui [2 ]
He, Xing-Xing [1 ]
机构
[1] Huazhong Univ Sci & Technol, Inst Liver Dis, Tongji Hosp, Tongji Med Coll, Wuhan 430030, Peoples R China
[2] Huazhong Univ Sci & Technol, Sch Pharm, Tongji Med Coll, Wuhan 430030, Peoples R China
[3] Ohio State Univ, Coll Pharm, Div Pharmaceut & Pharmaceut Chem, 500 W 12Th Ave, Columbus, OH 43210 USA
基金
中国国家自然科学基金;
关键词
microRNA; liver cancer; nanomedicine; therapy; AEG-1; LIVER-CANCER; MICRORNA EXPRESSION; MOUSE MODELS; IN-VITRO; SURVIVAL; CELLS;
D O I
10.18632/oncotarget.13431
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
MiR-375 is a tumor suppressor miRNA that is downregulated in hepatocellular carcinoma (HCC). However, due to the lack of effective delivery strategies, miR-375 replacement as a therapy for HCC has not been investigated. In the present study, we have developed a straightforward strategy to deliver miR-375 into HCC cells by assembling miR-375 mimics on the surface of AuNPs and forming AuNP-miR-375 nanoparticles. AuNP-miR-375 exhibits high cellular uptake and preserves miR-375's activities to suppress cellular proliferation, migration/invasion, and colony formation, and to induce apoptosis in HCC cells. Furthermore, AuNP-delivered miR-375 efficiently downregulated its target genes through RNA interference. In primary and xenograft tumor mouse models, AuNP-miR-375 showed high tumor uptake, therapeutic efficacy, and no apparent toxicity to the host mice. In conclusion, our findings indicate that AuNPs is a reliable strategy to deliver miR-375 into HCC cells and tissue, and that AuNP-miR-375 has the potential in the clinic for treatment of unresectable HCC.
引用
收藏
页码:86675 / 86686
页数:12
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