Label-free isolation of a prostate cancer cell among blood cells and the single-cell measurement of drug accumulation using an integrated microfluidic chip

被引:37
|
作者
Khamenehfar, A. [1 ]
Beischlag, T. V. [2 ]
Russell, P. J. [3 ]
Ling, M. T. P. [3 ]
Nelson, C. [3 ]
Li, P. C. H. [1 ]
机构
[1] Simon Fraser Univ, Dept Chem, Burnaby, BC V5A 1S6, Canada
[2] Simon Fraser Univ, Fac Hlth Sci, Burnaby, BC V5A 1S6, Canada
[3] Queensland Univ Technol, Australian Prostate Canc Res Ctr Queensland, Inst Hlth & Biomed Innovat, Dept Fac Hlth,Princess Alexandra Hosp,Translat Re, Brisbane, Qld 4001, Australia
基金
英国医学研究理事会; 加拿大自然科学与工程研究理事会;
关键词
CIRCULATING TUMOR-CELLS; ABC MULTIDRUG TRANSPORTERS; PROGRESSION-FREE; P-GLYCOPROTEIN; RESISTANCE; SEPARATION; EXPRESSION; MICROCHIP; ANDROGEN; EFFLUX;
D O I
10.1063/1.4934715
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Circulating tumor cells (CTCs) are found in the blood of patients with cancer. Although these cells are rare, they can provide useful information for chemotherapy. However, isolation of these rare cells from blood is technically challenging because they are small in numbers. An integrated microfluidic chip, dubbed CTC chip, was designed and fabricated for conducting tumor cell isolation. As CTCs usually show multidrug resistance (MDR), the effect of MDR inhibitors on chemotherapeutic drug accumulation in the isolated single tumor cell is measured. As a model of CTC isolation, human prostate cancer cells were mixed with mouse blood cells and the label-free isolation of the tumor cells was conducted based on cell size difference. The major advantages of the CTC chip are the ability for fast cell isolation, followed by multiple rounds of single-cell measurements, suggesting a potential assay for detecting the drug responses based on the liquid biopsy of cancer patients. (C) 2015 AIP Publishing LLC.
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页数:18
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