| Literature DB >> 28941584 |
Eric Lin1, Lianette Rivera-Báez1, Shamileh Fouladdel2, Hyeun Joong Yoon1, Stephanie Guthrie1, Jacob Wieger1, Yadwinder Deol3, Evan Keller2, Vaibhav Sahai2, Diane M Simeone4, Monika L Burness3, Ebrahim Azizi2, Max S Wicha5, Sunitha Nagrath6.
Abstract
We present "Labyrinth," a label-free microfluidic device to isolate circulating tumor cells (CTCs) using the combination of long loops and sharp corners to focus both CTCs and white blood cells (WBCs) at a high throughput of 2.5 mL/min. The high yield (>90%) and purity (600 WBCs/mL) of Labyrinth enabled us to profile gene expression in CTCs. As proof of principle, we used previously established cancer stem cell gene signatures to profile single cells isolated from the blood of breast cancer patients. We observed heterogeneous subpopulations of CTCs expressing genes for stem cells, epithelial cells, mesenchymal cells, and cells transitioning between epithelial and mesenchymal. Labyrinth offers a cell-surface marker-independent single-cell isolation platform to study heterogeneous CTC subpopulations.Entities:
Keywords: breast cancer; circulating tumor cells; epithelial mesenchymal transition; heterogeneity of cancer; label-free separation; mesenchymal epithelial transition; microfluidics; pancreatic cancer; single-cell gene analysis of CTCs
Mesh:
Year: 2017 PMID: 28941584 DOI: 10.1016/j.cels.2017.08.012
Source DB: PubMed Journal: Cell Syst ISSN: 2405-4712 Impact factor: 10.304