Microfluidic flow fractionation device for label-free isolation of circulating tumor cells (CTCs) from breast cancer patients

被引:107
作者
Hyun, Kyung-A [1 ]
Kwon, Kiho [1 ]
Han, Hyunju [2 ]
Kim, Seung-Il [2 ]
Jung, Hyo-Il [1 ]
机构
[1] Yonsei Univ, Sch Mech Engn, Seoul 120752, South Korea
[2] Yonsei Univ, Coll Med, Seoul 120752, South Korea
基金
新加坡国家研究基金会;
关键词
Circulating tumor cell; Metastasis; Flow fractionation; Breast cancer; SIZE-BASED SEPARATION; CONTRACTION/EXPANSION MICROCHANNELS; SERIES;
D O I
10.1016/j.bios.2012.07.021
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
Circulating tumor cells (CTCs) are dissociated from primary tumor and circulate in peripheral blood. They are regarded as the genesis of metastasis. Isolation and enumeration of CTCs serve as valuable tools for cancer prognosis and diagnosis. However, the rarity and heterogeneity of CTCs in blood makes it difficult to separate intact CTCs without loss. In this paper, we introduce a parallel multi-orifice flow fractionation (p-MOFF) device in which a series of contraction/expansion microchannels are placed parallel on a chip forming four identical channels. CTCs were continuously isolated from the whole blood of breast cancer patients by hydrodynamic forces and cell size differences. Blood samples from 24 breast cancer patients were analyzed (half were from metastatic breast cancer patients and the rest were from adjuvant breast cancer patients). The number of isolated CTCs varied from 0 to 21 in 7.5 ml of blood. Because our devices do not require any labeling processes (e.g.. EpCAM antibody), heterogeneous CTCs can be isolated regardless of EpCAM expression. (C) 2012 Elsevier B.V. All rights reserved.
引用
收藏
页码:206 / 212
页数:7
相关论文
共 17 条
[1]   Separation and detection of rare cells in a microfluidic disk via negative selection [J].
Chen, Chen-Lin ;
Chen, Ken-Chao ;
Pan, Yu-Cheng ;
Lee, Tai-Ping ;
Hsiung, Lo-Chang ;
Lin, Cheng-Ming ;
Chen, Chang-Yu ;
Lin, Ching-Hung ;
Chiang, Bor-Luen ;
Wo, Andrew M. .
LAB ON A CHIP, 2011, 11 (03) :474-483
[2]   Circulating tumor cells: A novel prognostic factor for newly diagnosed metastatic breast cancer [J].
Cristofanilli, M ;
Hayes, DF ;
Budd, GT ;
Ellis, MJ ;
Stopeck, A ;
Reuben, JM ;
Doyle, GV ;
Matera, J ;
Allard, WJ ;
Miller, MC ;
Fritsche, HA ;
Hortobagyi, GN ;
Terstappen, LWMM .
JOURNAL OF CLINICAL ONCOLOGY, 2005, 23 (07) :1420-1430
[3]   Circulating tumor cells: the Grand Challenge [J].
den Toonder, Jaap .
LAB ON A CHIP, 2011, 11 (03) :375-377
[4]   Microsystems for isolation and electrophysiological analysis of breast cancer cells from blood [J].
Han, KH ;
Han, A ;
Frazier, AB .
BIOSENSORS & BIOELECTRONICS, 2006, 21 (10) :1907-1914
[5]  
Hou Jian-Mei, 2010, Cancers (Basel), V2, P1236, DOI 10.3390/cancers2021236
[6]   High speed detection of circulating tumor cells [J].
Hsieh, HB ;
Marrinucci, D ;
Bethel, K ;
Curry, DN ;
Humphrey, M ;
Krivacic, RT ;
Kroener, J ;
Kroener, L ;
Ladanyi, A ;
Lazarus, N ;
Kuhn, P ;
Bruce, RH ;
Nieva, J .
BIOSENSORS & BIOELECTRONICS, 2006, 21 (10) :1893-1899
[7]   Circulating Tumor Cells: Detection Methods and Potential Clinical Application in Breast Cancer [J].
Kim, Seung Il ;
Jung, Hyo-il .
JOURNAL OF BREAST CANCER, 2010, 13 (02) :125-131
[8]  
Moon HS, 2011, LAB CHIP, V11, P1118, DOI [10.1039/c0lc00345j, 10.1039/c01c00345j]
[9]   Isolation of rare circulating tumour cells in cancer patients by microchip technology [J].
Nagrath, Sunitha ;
Sequist, Lecia V. ;
Maheswaran, Shyamala ;
Bell, Daphne W. ;
Irimia, Daniel ;
Ulkus, Lindsey ;
Smith, Matthew R. ;
Kwak, Eunice L. ;
Digumarthy, Subba ;
Muzikansky, Alona ;
Ryan, Paula ;
Balis, Ulysses J. ;
Tompkins, Ronald G. ;
Haber, Daniel A. ;
Toner, Mehmet .
NATURE, 2007, 450 (7173) :1235-U10
[10]   Multiorifice Flow Fractionation: Continuous Size-Based Separation of Microspheres Using a Series of Contraction/Expansion Microchannels [J].
Park, Jae-Sung ;
Jung, Hyo-Il .
ANALYTICAL CHEMISTRY, 2009, 81 (20) :8280-8288