适体
循环肿瘤细胞
液体活检
DNA
掩蔽
自愈水凝胶
化学
上皮细胞粘附分子
细胞
癌细胞
单细胞分析
细胞粘附
生物物理学
核酸
微流控
纳米技术
生物传感器
癌症
细胞生物学
分子生物学
生物
遗传学
生物化学
转移
有机化学
作者
Ping Song,Dekai Ye,Xiaolei Zuo,Jiang Li,Jianbang Wang,Huajie Liu,Michael Taeyoung Hwang,Jie Chao,Shao Su,Lihua Wang,Jiye Shi,Lianhui Wang,Wei Huang,Ratnesh Lal,Fan Chen
出处
期刊:Nano Letters
[American Chemical Society]
日期:2017-08-10
卷期号:17 (9): 5193-5198
被引量:183
标识
DOI:10.1021/acs.nanolett.7b01006
摘要
Circulating tumor cells (CTCs) contain molecular information on the primary tumor and can be used for predictive cancer diagnostics. Capturing rare live CTCs and their quantification in whole blood remain technically challenging. Here we report an aptamer-trigger clamped hybridization chain reaction (atcHCR) method for in situ identification and subsequent cloaking/decloaking of CTCs by porous DNA hydrogels. These decloaked CTCs were then used for live cell analysis. In our design, a DNA staple strand with aptamer-toehold biblocks specifically recognizes epithelial cell adhesion molecule (EpCAM) on the CTC surface that triggers subsequent atcHCR via toehold-initiated branch migration. Porous DNA hydrogel based-cloaking of single/cluster of CTCs allows capturing of living CTCs directly with minimal cell damage. The ability to identify a low number of CTCs in whole blood by DNA hydrogel cloaking would allow high sensitivity and specificity for diagnosis in clinically relevant settings. More significantly, decloaking of CTCs using controlled and defined chemical stimuli can release living CTCs without damages for subsequent culture and live cell analysis. We expect this liquid biopsy tool to open new powerful and effective routes for cancer diagnostics and therapeutics.
科研通智能强力驱动
Strongly Powered by AbleSci AI