DNA aptamer selected for specific recognition of prostate cancer cells and clinical tissues

被引:0
作者
Zhi-Xiang Huang [1 ]
Qin Xie [1 ]
Qiu-Ping Guo [1 ]
Ke-Min Wang [1 ]
Xiang-Xian Meng [1 ]
Bao-Yin Yuan [1 ]
Jun Wan [1 ]
Yuan-Yuan Chen [1 ]
机构
[1] State Key Laboratory of Chemo/Biosensing and Chemometrics,College of Biology,College of Chemistry and Chemical Engineering,Key Laboratory for Bio-Nanotechnology and Molecular Engineering of Hunan Province,Hunan University
基金
中国国家自然科学基金;
关键词
Aptamer; Cell-SELEX; Prostate cancer; PC-3M; Clinical tissues;
D O I
暂无
中图分类号
R737.25 [前列腺肿瘤];
学科分类号
100214 ;
摘要
Prostate cancer is the most common malignancy in men lack of efficient early diagnosis and therapeutics,calling for effective molecular probes.Herein,we performed cell-based systematic evolution of ligands by exponential enrichment(cell-SELEX) to obtain specific recognition of human prostate cancer cells PC-3M.Four aptamers were successfully obtained that can bind to target cells with high affinity and specificity.A 51-nt truncated sequence named Xq-2-C1 was identified after further elaborative analysis on the secondary structure.More importantly,the achieved aptamer Xq-2-C1 not only demonstrated excellent specific to target cells,but also revealed specific recognition to clinical prostate cancer tissue.The tissue imaging results showed that Xq-2-C1 had better recognition ratio for clinical prostate cancer tissue samples(85%) compared to the random sequence(9%).These results demonstrate that these newly generated aptamers would furnish potential applications in the early diagnosis and clinical treatment of prostate cancer.
引用
收藏
页码:1252 / 1257
页数:6
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