Department of Imaging Physics Research, The University of Texas, M.D. Anderson Cancer Center Unit 951, 1515 Holcombe Boulevard, Houston, Texas 77030, USA ; Department of Biomedical Engineering, The University of Texas at Austin, 1 University Station, C0800, Austin, Texas 78712, USA.
Department of Systems Biology, The University of Texas, M.D. Anderson Cancer Center Unit 951, 1515 Holcombe Boulevard, Houston, Texas 77030, USA.
Biomicrofluidics. 2013 Jan 16;7(1):11808. doi: 10.1063/1.4774307. eCollection 2013.
The number of circulating tumor cells (CTCs) found in blood is known to be a prognostic marker for recurrence of primary tumors, however, most current methods for isolating CTCs rely on cell surface markers that are not universally expressed by CTCs. Dielectrophoresis (DEP) can discriminate and manipulate cancer cells in microfluidic systems and has been proposed as a molecular marker-independent approach for isolating CTCs from blood. To investigate the potential applicability of DEP to different cancer types, the dielectric and density properties of the NCI-60 panel of tumor cell types have been measured by dielectrophoretic field-flow fractionation (DEP-FFF) and compared with like properties of the subpopulations of normal peripheral blood cells. We show that all of the NCI-60 cell types, regardless of tissue of origin, exhibit dielectric properties that facilitate their isolation from blood by DEP. Cell types derived from solid tumors that grew in adherent cultures exhibited dielectric properties that were strikingly different from those of peripheral blood cell subpopulations while leukemia-derived lines that grew in non-adherent cultures exhibited dielectric properties that were closer to those of peripheral blood cell types. Our results suggest that DEP methods have wide applicability for the surface-marker independent isolation of viable CTCs from blood as well as for the concentration of leukemia cells from blood.
血液中循环肿瘤细胞 (CTC) 的数量已知是原发性肿瘤复发的预后标志物,然而,目前大多数分离 CTC 的方法都依赖于并非普遍表达于 CTC 上的细胞表面标志物。介电泳 (DEP) 可在微流控系统中区分和操纵癌细胞,并已被提议作为一种与分子标志物无关的方法,从血液中分离 CTC。为了研究 DEP 对不同癌症类型的潜在适用性,通过介电泳场流分级 (DEP-FFF) 测量了 NCI-60 肿瘤细胞类型面板的介电和密度特性,并将其与正常外周血细胞亚群的类似特性进行了比较。我们表明,所有 NCI-60 细胞类型,无论其起源组织如何,都表现出有助于通过 DEP 从血液中分离的介电特性。在贴壁培养中生长的源自实体瘤的细胞类型表现出与外周血细胞亚群明显不同的介电特性,而在非贴壁培养中生长的白血病衍生系则表现出与外周血细胞类型更接近的介电特性。我们的结果表明,DEP 方法具有广泛的适用性,可用于从血液中分离表面标志物独立的存活 CTC,以及从血液中浓缩白血病细胞。