Circulating Tumor Cell Enrichment Based on Physical Properties

被引:125
作者
Harouaka, Ramdane A. [1 ,2 ,3 ]
Nisic, Merisa [1 ,2 ,3 ]
Zheng, Si-Yang [1 ,2 ,3 ]
机构
[1] Penn State Univ, Dept Bioengn, Micro & Nano Integrated Biosyst MINIBio Lab, University Pk, PA 16802 USA
[2] Penn State Univ, Mat Res Inst, University Pk, PA 16802 USA
[3] Penn State Hershey Canc Inst, Hershey, PA USA
来源
JALA | 2013年 / 18卷 / 06期
基金
美国国家卫生研究院;
关键词
circulating tumor cells; cancer; physical properties; antigen-independent; enrichment; METASTATIC BREAST-CANCER; ACUTE MYELOID-LEUKEMIA; PERIPHERAL-BLOOD; DIELECTRIC-PROPERTIES; STEM-CELLS; CLINICAL-SIGNIFICANCE; FORCE MICROSCOPY; BIOLOGICAL CELLS; PROGRESSION-FREE; RARE CELLS;
D O I
10.1177/2211068213494391
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
The metastatic dissemination and spread of malignant circulating tumor cells (CTCs) accounts for more than 90% of cancer-related deaths. CTCs detach from a primary tumor, travel through the circulatory system, and then invade and proliferate in distant organs. The detection of CTCs from blood has been established for prognostic monitoring and is predictive of patient outcome. Analysis of CTCs could enable the means for early detection and screening in cancer, as well as provide diagnostic access to tumor tissues in a minimally invasive way. The fundamental challenge with analyzing CTCs is the fact that they occur at extremely low concentrations in blood, on the order of one out of a billion cells. Various technologies have been proposed to isolate CTCs for enrichment. Here we focus on antigen-independent approaches that are not limited by specific capture antibodies. Intrinsic physical properties of CTCs, including cell size, deformability, and electrical properties, are reviewed, and technologies developed to exploit them for enrichment from blood are summarized. Physical enrichment technologies are of particular interest as they have the potential to increase yield and enable the analysis of rare CTC phenotypes that may not be otherwise obtained.
引用
收藏
页码:455 / 468
页数:14
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