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PillarX:一种基于几何形状、变形能力和上皮状态对循环肿瘤细胞簇进行分析的微流控装置。

PillarX: A Microfluidic Device to Profile Circulating Tumor Cell Clusters Based on Geometry, Deformability, and Epithelial State.

机构信息

IFOM-FIRC Institute of Molecular Oncology, Via Adamello, 16, Milan, 20139, Italy.

IEO, Istituto Europeo di Oncologia IRCCS, Via Ripamonti 435, Milan, 20141, Italy.

出版信息

Small. 2022 Apr;18(17):e2106097. doi: 10.1002/smll.202106097. Epub 2022 Mar 28.

DOI:10.1002/smll.202106097
PMID:35344274
Abstract

Circulating tumor cell (CTC) clusters are associated with increased metastatic potential and worse patient prognosis, but are rare, difficult to count, and poorly characterized biophysically. The PillarX device described here is a bimodular microfluidic device (Pillar-device and an X-magnetic device) to profile single CTCs and clusters from whole blood based on their size, deformability, and epithelial marker expression. Larger, less deformable clusters and large single cells are captured in the Pillar-device and sorted according to pillar gap sizes. Smaller, deformable clusters and single cells are subsequently captured in the X-device and separated based on epithelial marker expression using functionalized magnetic nanoparticles. Clusters of established and primary breast cancer cells with variable degrees of cohesion driven by different cell-cell adhesion protein expression are profiled in the device. Cohesive clusters exhibit a lower deformability as they travel through the pillar array, relative to less cohesive clusters, and have greater collective invasive behavior. The ability of the PillarX device to capture clusters is validated in mouse models and patients of metastatic breast cancer. Thus, this device effectively enumerates and profiles CTC clusters based on their unique geometrical, physical, and biochemical properties, and could form the basis of a novel prognostic clinical tool.

摘要

循环肿瘤细胞 (CTC) 簇与转移潜能增加和患者预后不良相关,但数量稀少、难以计数且物理特性描述不佳。本文介绍的 PillarX 设备是一种双模块微流控设备(Pillar 设备和 X 磁设备),可根据大小、变形性和上皮标志物表达对来自全血的单个 CTC 和簇进行分析。较大、变形性较小的簇和较大的单个细胞在 Pillar 设备中被捕获,并根据柱间隙大小进行分类。较小、变形性较大的簇和单个细胞随后在 X 设备中被捕获,并根据上皮标志物表达使用功能化磁性纳米颗粒进行分离。在设备中对具有不同细胞间黏附蛋白表达驱动的不同黏附程度的已建立和原发性乳腺癌细胞簇进行分析。与黏附性较小的簇相比,在穿过柱阵列时,具有较高黏附性的簇表现出较低的变形性,并且具有更强的集体侵袭行为。PillarX 设备在转移性乳腺癌的小鼠模型和患者中验证了其捕获簇的能力。因此,该设备可根据 CTC 簇的独特几何、物理和生化特性有效对其进行计数和分析,并且可能成为一种新的预后临床工具的基础。

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