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Comprehensive Single Cell Microfluidic Chips for the Study of Cancer Cell Heterogeneity and Metastasis.

机译:综合单细胞微流控芯片研究癌细胞异质性和转移。

摘要

Due to the genomic and epigenetic instability of cancer cells, tumors are highly heterogeneous and difficult to treat. Additionally, cancer metastasis, which account for 90% of cancer mortality, is a complicated multi-step process. As such ideal assays should be high-throughput and providesingle-cell resolution and microenvironmet control, enlighteningindividual cellpropertiesrather than the average behavior of the bulk tumor. Here, we have developed microfluidic platforms meeting these requirements to investigate three critical stages of metastasis.First, asingle-cell migration chipwas developed to model cancer cell migration from the primary tumor. The motility of cells under the influence of chemo-attractants can be measuredon-chip. After the assays, highly motile cells and non-motile cells can be retrieved for further culture and analysis. Second, to understand cell survival in the circulatory system, a single-cell suspension culture chipwas developed, improving the throughput of single-cell anoikis assays and single-cell derived sphere formation by orders of magnitudeutilizing hydrodynamic single cell positioning.Third, to investigate interactions between cancer cells and stromal cells, three cell-cell interaction platforms were developed. Innovations including control of interacting cell ratios, valveless isolation of co-culture using two-phase flow, continuous nutrient renewal enabled by 3D integration, and dual adherent-suspension co-culture were attained.In addition, a selective single-cell retrieval technique that selectively detaches and retrieves targeted single cells has been developed for incorporation in our microfluidic platforms. The technique neither affects cell viability nor alters mRNA expression for qRT-PCR. These single cell platforms provide numerous advantages over traditional methods including: (1) ability to monitor and track individual cells, (2) control of various micro-environments on-chip for emulation of bio-processes, (3) accommodation of high-throughput screening, (4) capability to handle rare cell samples, and(5) potential to retrieve interesting single cells for further culture and analysis.
机译:由于癌细胞的基因组和表观遗传的不稳定性,肿瘤高度异质且难以治疗。此外,占90%的癌症死亡率的癌症转移是一个复杂的多步骤过程。因此,理想的测定方法应该是高通量的,并提供单细胞分辨率和微环境控制,从而启发单个细胞的特性,而不是大块肿瘤的平均行为。在这里,我们开发了满足这些要求的微流体平台,以研究转移的三个关键阶段。首先,开发了单细胞迁移芯片来模拟癌细胞从原发肿瘤的迁移。可以在芯片上测量在化学吸引剂的影响下细胞的运动性。在测定之后,可以回收高运动能力的细胞和非运动能力的细胞用于进一步的培养和分析。其次,为了了解循环系统中的细胞存活率,开发了单细胞悬浮培养芯片,通过利用流体动力学单细胞定位将数量级提高了单细胞阳极测定和单细胞衍生球形成的通量。第三,研究相互作用在癌细胞和基质细胞之间,开发了三个细胞-细胞相互作用平台。创新包括控制相互作用的细胞比例,使用两相流进行无瓣膜分离共培养,通过3D集成实现连续养分更新以及双重粘附-悬浮共培养。此外,还获得了一种选择性单细胞检索技术选择性分离并回收靶向的单细胞已被开发用于整合到我们的微流体平台中。该技术既不会影响细胞生存力,也不会改变qRT-PCR的mRNA表达。与传统方法相比,这些单细胞平台具有许多优势,包括:(1)监视和跟踪单个细胞的能力;(2)芯片上各种微环境的控制以模拟生物过程;(3)高通量的适应性筛选,(4)处理稀有细胞样品的能力和(5)检索有趣​​的单细胞用于进一步培养和分析的潜力。

著录项

  • 作者

    Chen Yu-Chih;

  • 作者单位
  • 年度 2014
  • 总页数
  • 原文格式 PDF
  • 正文语种 en_US
  • 中图分类
  • 入库时间 2022-08-31 16:10:14

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