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基于生物正交化学的细胞释放磁性囊泡捕获代谢标记的稀有循环肿瘤细胞。

Cell-Released Magnetic Vesicles Capturing Metabolic Labeled Rare Circulating Tumor Cells Based on Bioorthogonal Chemistry.

机构信息

National Engineering Research Center for Biomaterials, Sichuan University, Chengdu, 610064, P. R. China.

出版信息

Small. 2021 May;17(18):e2007796. doi: 10.1002/smll.202007796. Epub 2021 Mar 21.

Abstract

Capture of circulating tumor cells (CTCs) with high efficiency and high purity holds great value for potential clinical applications. Besides the existing problems of contamination from blood cells and plasma proteins, unknown/down-regulated expression of targeting markers (e.g., antigen, receptor, etc.) of CTCs have questioned the reliability and general applicability of current CTCs capture methodologies based on immune/aptamer-affinity. Herein, a cell-engineered strategy is designed to break down such barriers by employing the cell metabolism as the leading force to solve key problems. Generally, through an extracellular vesicle generation way, the cell-released magnetic vesicles inherited parent cellular membrane characteristics are produced, and then functionalized with dibenzoazacyclooctyne to target and isolate the metabolic labeled rare CTCs. This strategy offers good reliability and broader possibilities to capture different types of tumor cells, as proven by the capture efficiency above 84% and 82% for A549 and HepG2 cell lines as well as an extremely low detection limitation of 5 cells. Moreover, it enabled high purity enrichment of CTCs from 1 mL blood samples of tumor-bearing mice, only ≈5-757 white blood cells are non-specific caught, ignoring the potential phenotypic fluctuation associated with the cancer progression.

摘要

高效、高纯度地捕获循环肿瘤细胞 (CTC) 在潜在的临床应用中具有重要价值。除了现有的血细胞和血浆蛋白污染问题外,CTC 靶向标志物(如抗原、受体等)的未知/下调表达也质疑了基于免疫/适体亲和力的当前 CTC 捕获方法的可靠性和普遍适用性。在此,设计了一种基于细胞工程的策略,通过利用细胞代谢作为主要驱动力来解决关键问题,从而打破这些障碍。通常,通过细胞外囊泡生成途径,产生了具有亲本细胞膜特性的细胞释放的磁性囊泡,然后用二苯并氮杂环辛炔进行功能化,以靶向和分离代谢标记的稀有 CTC。该策略通过捕获效率超过 84%和 82%的 A549 和 HepG2 细胞系以及极低的检测极限 5 个细胞,证明了对不同类型肿瘤细胞具有良好的可靠性和更广泛的可能性。此外,它能够从荷瘤小鼠的 1ml 血液样本中高度纯净化 CTC,仅 ≈5-757 个白细胞被非特异性捕获,忽略了与癌症进展相关的潜在表型波动。

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