In vivo SELEX of bone targeting aptamer in prostate cancer bone metastasis model

被引:38
作者
Chen, Lingxiao [1 ]
He, Wei [1 ]
Jiang, Huichuan [1 ]
Wu, Longxiang [1 ]
Xiong, Wei [1 ]
Li, Bolun [1 ]
Zhou, Zhihua [2 ]
Qian, Yuna [3 ,4 ,5 ]
机构
[1] Cent South Univ, Xiangya Hosp, Dept Urol, Changsha 410008, Hunan, Peoples R China
[2] Hunan Univ Sci & Technol, Sch Chem & Chem Engn, Xiangtan 411201, Hunan, Peoples R China
[3] Chinese Acad Sci, Wenzhou Inst Biomat & Engn, Wenzhou 325001, Zhejiang, Peoples R China
[4] Wenzhou Med Univ, Sch Biomed Engn, Sch Ophthalmol & Optometry, Xinsan Rd 16,R1307, Wenzhou 325035, Zhejiang, Peoples R China
[5] Chongqing Univ, Minist Educ, Key Lab Biorheol Sci & Technol, Chongqing 400045, Peoples R China
关键词
aptamer; tumor endothelial targeting; drug delivery; TUMOR-GROWTH; ANGIOGENESIS; INHIBITION; DELIVERY;
D O I
10.2147/IJN.S188003
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Purpose: PB is one of the most severe complications of late stage prostate cancer and negatively impacts patient quality of life. A major challenge for the treatment of cancer bone metastasis is the management of efficient drug delivery to metastatic bone lesion. We aimed to explore the use of aptamers as promising tools to develop a targeted drug delivery system for PBs. Materials and methods: In vivo SELEX was applied to identify bone targeting aptamer in a mouse model with PBs. Results: The aptamer (designated as "PB") with the highest bone targeting frequency in mice bearing PC3 PB was selected for further analysis. The PB aptamer specifically targeted modulated endothelial cells in response to cancer cells in the bones of mice bearing PC3 PBs. The targeting efficiency of the PB aptamer conjugated to gold particles was verified in vivo. Conclusion: This investigation highlights the promise of in vivo SELEX for the discovery of bone targeting aptamers for use in drug delivery.
引用
收藏
页码:149 / 159
页数:11
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