ApoCell, Inc., Houston, Texas 77054, USA.
Biomicrofluidics. 2012 Jun 27;6(2):24133. doi: 10.1063/1.4731647. Print 2012 Jun.
Isolation and enumeration of circulating tumor cells (CTCs) are used to monitor metastatic disease progression and guide cancer therapy. However, currently available technologies are limited to cells expressing specific cell surface markers, such as epithelial cell adhesion molecule (EpCAM) or have limited specificity because they are based on cell size alone. We developed a device, ApoStream(™) that overcomes these limitations by exploiting differences in the biophysical characteristics between cancer cells and normal, healthy blood cells to capture CTCs using dielectrophoretic technology in a microfluidic flow chamber. Further, the system overcomes throughput limitations by operating in continuous mode for efficient isolation and enrichment of CTCs from blood. The performance of the device was optimized using a design of experiment approach for key operating parameters such as frequency, voltage and flow rates, and buffer formulations. Cell spiking studies were conducted using SKOV3 or MDA-MB-231 cell lines that have a high and low expression level of EpCAM, respectively, to demonstrate linearity and precision of recovery independent of EpCAM receptor levels. The average recovery of SKOV3 and MDA-MB-231 cancer cells spiked into approximately 12 × 10(6) peripheral blood mononuclear cells obtained from 7.5 ml normal human donor blood was 75.4% ± 3.1% (n = 12) and 71.2% ± 1.6% (n = 6), respectively. The intra-day and inter-day precision coefficients of variation of the device were both less than 3%. Linear regression analysis yielded a correlation coefficient (R(2)) of more than 0.99 for a spiking range of 4-2600 cells. The viability of MDA-MB-231 cancer cells captured with ApoStream was greater than 97.1% and there was no difference in cell growth up to 7 days in culture compared to controls. The ApoStream device demonstrated high precision and linearity of recovery of viable cancer cells independent of their EpCAM expression level. Isolation and enrichment of viable cancer cells from ApoStream enables molecular characterization of CTCs from a wide range of cancer types.
循环肿瘤细胞(CTCs)的分离和计数用于监测转移性疾病的进展并指导癌症治疗。然而,目前可用的技术仅限于表达特定细胞表面标志物的细胞,例如上皮细胞黏附分子(EpCAM),或者由于仅基于细胞大小而特异性有限。我们开发了一种设备,ApoStream(™),通过利用癌细胞和正常健康血细胞之间的生物物理特性差异来克服这些限制,该设备使用介电泳技术在微流控流动室中捕获 CTCs。此外,该系统通过连续模式操作克服了通量限制,从而有效地从血液中分离和富集 CTCs。使用实验设计方法优化了设备的性能,用于关键操作参数,如频率、电压和流速以及缓冲液配方。使用 SKOV3 或 MDA-MB-231 细胞系进行细胞加标研究,这些细胞系的 EpCAM 表达水平分别较高和较低,以证明与 EpCAM 受体水平无关的恢复的线性和精密度。从 7.5 ml 正常人类供体血液中获得的大约 12×10(6)个外周血单核细胞中加入 SKOV3 和 MDA-MB-231 癌细胞的平均回收率分别为 75.4%±3.1%(n=12)和 71.2%±1.6%(n=6)。该设备的日内和日间精密度变异系数均小于 3%。在 4-2600 个细胞的加标范围内,线性回归分析得到的相关系数(R(2))大于 0.99。用 ApoStream 捕获的 MDA-MB-231 癌细胞的活力大于 97.1%,与对照相比,在培养中长达 7 天的细胞生长没有差异。ApoStream 设备显示出高的精度和与 EpCAM 表达水平无关的活癌细胞的恢复的线性。从 ApoStream 中分离和富集活癌细胞能够对来自广泛癌症类型的 CTCs 进行分子表征。