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Bioinspired DNA Nanointerface with Anisotropic Aptamers for Accurate Capture of Circulating Tumor Cells

机译:具有各向异性适体的Bioinspired DNA纳米迹用于精确捕获循环肿瘤细胞

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摘要

The capture and analysis of circulating tumor cells (CTCs) have provided a non‐invasive entry for cancer diagnosis and disease monitoring. Despite recent development in affinity‐based CTCs isolation, it remains challenging to achieve efficient capture toward CTCs with dynamic surface expression. Enlightened by the synergistic effect insideimmune synapses, the development of a nanointerface engineered with topology‐defined anisotropic aptamers programmed by DNA scaffold (DNA nanosynapse), for accurate CTCs isolation, is herein reported. As compared to isotropic aptamers, the DNA nanosynapse exhibits enhanced anchoring on the cell membrane with both high and low epithelial cell adhesion molecule (EpCAM) expression. This nanointerface enables accurate capture toward CTCs of heterogeneous EpCAM, without dramatically proportional change inside the mixture of diverse phenotypes. By applying this nanoplatform, CTCs detection as well as downstream analysis for measuring disease status can be achieved in clinical samples from breast cancer patients.
机译:循环肿瘤细胞(CTCs)的捕获和分析为癌症诊断和疾病监测提供了非侵入性进入。尽管最近基于亲和力的CTCS分离的发展,但在具有动态表面表达的情况下实现有效捕获仍然有挑战性。通过Ineximmune突触的协同效果开明,本文报道了通过DNA支架(DNA纳米型)编程的拓扑定义的各向异性适体,用于精确CTCS分离的拓扑定义的各向异性适体进行设计的开发。与各向同性的适体相比,DNA纳米肌腱表现出在细胞膜上具有增强的锚固,具有高和低上皮细胞粘附分子(EPCAM)表达。该纳米接口能够精确地捕获异构EPCAM的CTC,而没有在不同表型的混合物内部的显着成比例变化。通过施加该纳米片,可以在乳腺癌患者的临床样本中实现CTCS检测以及测量疾病状态下游分析。

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