Mechanical Low-Pass Filtering of Cells for Detection of Circulating Tumor Cells in Whole Blood.
Taiki SuzukiNoritada KajiHirotoshi YasakiTakao YasuiYoshinobu BabaPublished in: Analytical chemistry (2020)
The detection of circulating tumor cells (CTCs) from liquid biopsies using microfluidic devices is attracting a considerable amount of attention as a new, less-invasive cancer diagnostic and prognostic method. One of the drawbacks of the existing antibody-based detection systems is the false negatives for epithelial cell adhesion molecule detection of CTCs. Here we report a mechanical low-pass filtering technique based on a microfluidic constriction and electrical current sensing system for the novel CTC detection in whole blood without any specific antigen-antibody interaction or biochemical modification of the cell surface. The mechanical response of model cells of CTCs, such as HeLa, A549, and MDA-MB-231 cells, clearly demonstrated different behaviors from that of Jurkat cells, a human T-lymphocyte cell line, when they passed through the 6-μm wide constriction channel. A 6-μm wide constriction channel was determined as the optimum size to identify CTCs in whole blood with an accuracy greater than 95% in tens of milliseconds. The mechanical filtering of cells at a single cell level was achieved from whole blood without any pretreatment (e.g., dilution of lysing) and prelabeling (e.g., fluorophores or antibodies).
Keyphrases
- circulating tumor cells
- induced apoptosis
- cell cycle arrest
- single cell
- label free
- high throughput
- circulating tumor
- endoplasmic reticulum stress
- cell death
- loop mediated isothermal amplification
- neuropathic pain
- oxidative stress
- cell surface
- young adults
- squamous cell carcinoma
- spinal cord
- endothelial cells
- signaling pathway
- high resolution
- lymph node metastasis
- peripheral blood
- induced pluripotent stem cells