Abstract

Circulating tumor cells (CTCs) are a popular topic in cancer research because they can be obtained by liquid biopsy, a minimally invasive procedure with more sample accessibility than tissue biopsy, to monitor a patient’s condition. Over the past decades, CTC research has covered a wide variety of topics such as enumeration, profiling, and correlation between CTC number and patient overall survival. It is important to isolate and enrich CTCs before performing CTC analysis because CTCs in the blood stream are very rare (0–10 CTCs/mL of blood). Among the various approaches to separating CTCs, here, we review the research trends in the isolation and analysis of CTCs using microfluidics. Microfluidics provides many attractive advantages for CTC studies such as continuous sample processing to reduce target cell loss and easy integration of various functions into a chip, making “do-everything-on-a-chip” possible. However, tumor cells obtained from different sites within a tumor exhibit heterogenetic features. Thus, heterogeneous CTC profiling should be conducted at a single-cell level after isolation to guide the optimal therapeutic path. We describe the studies on single-CTC analysis based on microfluidic devices. Additionally, as a critical concern in CTC studies, we explain the use of CTCs in cancer research, despite their rarity and heterogeneity, compared with other currently emerging circulating biomarkers, including exosomes and cell-free DNA (cfDNA). Finally, the commercialization of products for CTC separation and analysis is discussed.

Highlights

  • Tumor cells form a three-dimensional shape and send signals to the nearby blood vessel network to form new blood networks near themselves in a process known as angiogenesis

  • We described the trends in Circulating tumor cells (CTCs) research and have divided the CTC study into three generations

  • The CTC isolations were processed with batch systems, but it was difficult to access a sufficient number of purified CTCs for analysis (1st generation)

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Summary

Introduction

Tumor cells form a three-dimensional shape and send signals to the nearby blood vessel network to form new blood networks near themselves in a process known as angiogenesis. Since the introduction of the CellSearch system in 2004, many researchers have studied the relationship between the number of CTCs and the survival rate [3] This is a powerful system for clinical application, but it has a comparably low detecting accuracy and is not able to distinguish between heterogenic tumor cell types. The heterogeneity such as different cell sizes and various protein expression levels on the surface is the inherent characteristic of cancer cells. A scale of 1 to 3 was used to rank each category, where 3 represents the highest score

Positive Enrichment of CTCs Using Antigen-Antibody Reaction
Negative Enrichment of CTCs
Integration of Enrichment Methods
Single CTC Analysis Using Microfluidic Devices
Critical Concerns
Commercialization of Microfluidic-Based CTC Research
Findings
Conclusions
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