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可扩展多层细胞收集器,用于捕获具有无限体积容量的循环肿瘤细胞。

Scalable Multilayer Cell Collector to Capture Circulating Tumor Cells with an Unlimited Volume Capacity.

作者信息

Tsai Yu-Lin, Yeh Po-Ying, Huang Chun-Jen, Guo Chin-Lin, Chang Ying-Chih

机构信息

Department of Chemical Engineering, Stanford University, 443 Via Ortega, Stanford, California 94305, United States.

Department of Biomedical Sciences and Engineering & Department of Chemical and Materials Engineering, National Central University, Taoyuan 320, Taiwan.

出版信息

ACS Biomater Sci Eng. 2019 Jun 10;5(6):2725-2731. doi: 10.1021/acsbiomaterials.9b00315. Epub 2019 May 22.

Abstract

Circulating tumor cells (CTCs) have been suggested as the precursors of metastatic cancer. CTC-based characterization has thus been used to monitor tumor status before the onset of metastasis and has shown to be an independent factor. The low abundance of CTCs, however, makes it challenging to employ CTC as a clinical routine, thus making it impossible to address tumor heterogeneity. Here, we present a cell collection prototype for an efficient capture of CTCs from a large volume of body fluids such as blood. An antibody-PEG modified multilayer matrix column is engineered and connected to an apheresis-based circulation system. This setup allows us to capture CTCs repetitively from an unlimited sample volume through the circulation system, thereby increasing the capture count. Compared to conventional CTC capturing devices where the sample handling is generally limited to 1-10 mL, our collector is able to handle a wide range of fluidic sample (40-2000 mL) at a high flow rate (400 mL/min). By processing 90 min in circulation, we obtained an average capture efficiency of at least 75% for the colorectal cancer cell line HCT116 spiked in either 40-200 mL of buffer solution or 40 mL of a whole blood sample. This result highlights a possibility to construct personalized CTC libraries through high-throughput CTC collection for the study of tumor heterogeneity in precision medicine.

摘要

循环肿瘤细胞(CTCs)被认为是转移性癌症的前体。因此,基于CTCs的特征分析已被用于在转移发生之前监测肿瘤状态,并且已被证明是一个独立因素。然而,CTCs的低丰度使得将其作为临床常规应用具有挑战性,从而无法解决肿瘤异质性问题。在此,我们展示了一种细胞收集原型,用于从大量体液(如血液)中高效捕获CTCs。设计了一种抗体-聚乙二醇修饰的多层基质柱,并将其连接到基于血液成分单采的循环系统。这种设置使我们能够通过循环系统从无限量的样本中重复捕获CTCs,从而增加捕获数量。与传统的CTCs捕获装置相比,传统装置的样本处理量通常限制在1-10 mL,而我们的收集器能够在高流速(400 mL/min)下处理广泛的流体样本(40-2000 mL)。通过90分钟的循环处理,我们对添加到40-200 mL缓冲溶液或40 mL全血样本中的结肠癌细胞系HCT116获得了至少75%的平均捕获效率。这一结果凸显了通过高通量CTCs收集构建个性化CTCs文库以用于精准医学中肿瘤异质性研究的可能性。

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