Microfluidics and cancer: are we there yet?

被引:83
作者
Zhang, Zhuo [1 ]
Nagrath, Sunitha [1 ]
机构
[1] Univ Michigan, Dept Chem Engn, Ann Arbor, MI 48109 USA
基金
美国国家科学基金会;
关键词
Microfluidics; Cancer; Cancer diagnostics; Circulating tumor cells; Tumor biology; Bio MEMS; Cancer therapeutics; CIRCULATING TUMOR-CELLS; TOTAL ANALYSIS SYSTEMS; BREAST-CANCER; CYTOMETRIC ANALYSIS; PROTEIN EXPRESSION; PERIPHERAL-BLOOD; CARCINOMA CELLS; DEVICE; NANOTECHNOLOGY; MUTATIONS;
D O I
10.1007/s10544-012-9734-8
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
More than two decades ago, microfluidics began to show its impact in biological research. Since then, the field of microfluidics has evolving rapidly. Cancer is one of the leading causes of death worldwide. Microfluidics holds great promise in cancer diagnosis and also serves as an emerging tool for understanding cancer biology. Microfluidics can be valuable for cancer investigation due to its high sensitivity, high throughput, less material-consumption, low cost, and enhanced spatio-temporal control. The physical laws on microscale offer an advantage enabling the control of physics, biology, chemistry and physiology at cellular level. Furthermore, microfluidic based platforms are portable and can be easily designed for point-of-care diagnostics. Developing and applying the state of the art microfluidic technologies to address the unmet challenges in cancer can expand the horizons of not only fundamental biology but also the management of disease and patient care. Despite the various microfluidic technologies available in the field, few have been tested clinically, which can be attributed to the various challenges existing in bridging the gap between the emerging technology and real world applications. We present a review of role of microlfuidcs in cancer research, including the history, recent advances and future directions to explore where the field stand currently in addressing complex clinical challenges and future of it. This review identifies four critical areas in cancer research, in which microfluidics can change the current paradigm. These include cancer cell isolation, molecular diagnostics, tumor biology and high-throughput screening for therapeutics. In addition, some of our lab's current research is presented in the corresponding sections.
引用
收藏
页码:595 / 609
页数:15
相关论文
共 109 条
[1]   New frontiers in nanotechnology for cancer treatment [J].
Alexis, Frank ;
Rhee, June-Wha ;
Richie, Jerome P. ;
Radovic-Moreno, Aleksandar F. ;
Langer, Robert ;
Farokhzad, Omid C. .
UROLOGIC ONCOLOGY-SEMINARS AND ORIGINAL INVESTIGATIONS, 2008, 26 (01) :74-85
[2]   Tumor cells circulate in the peripheral blood of all major carcinomas but not in healthy subjects or patients with nonmalignant diseases [J].
Allard, WJ ;
Matera, J ;
Miller, MC ;
Repollet, M ;
Connelly, MC ;
Rao, C ;
Tibbe, AGJ ;
Uhr, JW ;
Terstappen, LWMM .
CLINICAL CANCER RESEARCH, 2004, 10 (20) :6897-6904
[3]   Micro total analysis systems. 2. Analytical standard operations and applications [J].
Auroux, PA ;
Iossifidis, D ;
Reyes, DR ;
Manz, A .
ANALYTICAL CHEMISTRY, 2002, 74 (12) :2637-2652
[4]   EpCAM (CD326) finding its role in cancer [J].
Baeuerle, P. A. ;
Gires, O. .
BRITISH JOURNAL OF CANCER, 2007, 96 (03) :417-423
[5]   Droplet microfluidic technology for single-cell high-throughput screening [J].
Brouzes, Eric ;
Medkova, Martina ;
Savenelli, Neal ;
Marran, Dave ;
Twardowski, Mariusz ;
Hutchison, J. Brian ;
Rothberg, Jonathan M. ;
Link, Darren R. ;
Perrimon, Norbert ;
Samuels, Michael L. .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2009, 106 (34) :14195-14200
[6]   Cytometric analysis of protein expression and apoptosis in human primary cells with a novel microfluidic chip-based system [J].
Chan, SDH ;
Luedke, G ;
Valer, M ;
Buhlmann, C ;
Preckel, T .
CYTOMETRY PART A, 2003, 55A (02) :119-125
[7]   Multi-step microfluidic device for studying cancer metastasis [J].
Chaw, K. C. ;
Manimaran, M. ;
Tay, E. H. ;
Swaminathan, S. .
LAB ON A CHIP, 2007, 7 (08) :1041-1047
[8]   A quantitative observation and imaging of single tumor cell migration and deformation using a multi-gap microfluidic device representing the blood vessel [J].
Chaw, K. C. ;
Manimaran, M. ;
Tay, Francis E. H. ;
Swaminathan, S. .
MICROVASCULAR RESEARCH, 2006, 72 (03) :153-160
[9]   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
[10]   Microfluidic isolation and transcriptome analysis of serum microvesicles [J].
Chen, Chihchen ;
Skog, Johan ;
Hsu, Chia-Hsien ;
Lessard, Ryan T. ;
Balaj, Leonora ;
Wurdinger, Thomas ;
Carter, Bob S. ;
Breakefield, Xandra O. ;
Toner, Mehmet ;
Irimia, Daniel .
LAB ON A CHIP, 2010, 10 (04) :505-511