Wu Wen-jun, Wang Zhi-hua, Wang Zhuo, Deng Yu-liang, Shi Qi-hui
Shanghai Center for Systems Biomedicine, Shanghai Jiaotong University, Shanghai 200240, China.
Yi Chuan. 2017 Jan 20;39(1):66-74. doi: 10.16288/j.yczz.16-217.
Circulating tumor cells (CTCs) are free tumor cells shed from tumor site and enter into blood circulation. CTCs represent a reliable source of tumor cells for the molecular characteristics of the original tumor. However, the extraordinary rarity of CTCs makes the subsequent molecular and functional analysis technically challenging. Here, we describe a one-step microfludics-based immunomagnetic isolation method to isolate CTCs directly from the whole blood of lung adenocarcinoma patients. This method avoids harsh sample preparation and enrichment steps, and therefore preserves the viability (>90%) of CTCs during the in vitro isolation. The isolated CTCs are enriched in small volume (80 μL) and cultured ex vivo that leads to successful ex vivo expansion. The expanded CTCs can be frozen and thawed, which shows cell line property. Genetic sequencing on EGFR、KRAS、PIK3CA、TP53 and BRAF and metabolic assay (2-NBDG) are utilized to characterize the expanded CTCs. Our results demostrated that this method is suitable for ex vivo expansion of CTCs facilitates. The genomic, proteomic and metabolic analyses of CTCs have guiding significance in tumor precise treatment.
循环肿瘤细胞(CTCs)是从肿瘤部位脱落并进入血液循环的游离肿瘤细胞。CTCs是用于分析原发肿瘤分子特征的可靠肿瘤细胞来源。然而,CTCs极其稀少,这使得后续的分子和功能分析在技术上具有挑战性。在此,我们描述了一种基于微流控的一步免疫磁珠分离方法,可直接从肺腺癌患者的全血中分离CTCs。该方法避免了苛刻的样本制备和富集步骤,因此在体外分离过程中保留了CTCs的活力(>90%)。分离出的CTCs在小体积(80μL)中得到富集,并进行体外培养,从而实现了成功的体外扩增。扩增后的CTCs可进行冻融,表现出细胞系特性。利用对EGFR、KRAS、PIK3CA、TP53和BRAF的基因测序以及代谢分析(2-NBDG)来表征扩增后的CTCs。我们的结果表明,该方法适用于CTCs的体外扩增,对CTCs的基因组、蛋白质组和代谢分析在肿瘤精准治疗中具有指导意义。