Campton Daniel E, Ramirez Arturo B, Nordberg Joshua J, Drovetto Nick, Clein Alisa C, Varshavskaya Paulina, Friemel Barry H, Quarre Steve, Breman Amy, Dorschner Michael, Blau Sibel, Blau C Anthony, Sabath Daniel E, Stilwell Jackie L, Kaldjian Eric P
RareCyte, Inc, Seattle, WA, USA.
Departments of Laboratory Medicine and Medicine, University of Washington, Washington, USA.
BMC Cancer. 2015 May 6;15:360. doi: 10.1186/s12885-015-1383-x.
Circulating tumor cells (CTCs) are malignant cells that have migrated from solid cancers into the blood, where they are typically present in rare numbers. There is great interest in using CTCs to monitor response to therapies, to identify clinically actionable biomarkers, and to provide a non-invasive window on the molecular state of a tumor. Here we characterize the performance of the AccuCyte®--CyteFinder® system, a comprehensive, reproducible and highly sensitive platform for collecting, identifying and retrieving individual CTCs from microscopic slides for molecular analysis after automated immunofluorescence staining for epithelial markers.
All experiments employed a density-based cell separation apparatus (AccuCyte) to separate nucleated cells from the blood and transfer them to microscopic slides. After staining, the slides were imaged using a digital scanning microscope (CyteFinder). Precisely counted model CTCs (mCTCs) from four cancer cell lines were spiked into whole blood to determine recovery rates. Individual mCTCs were removed from slides using a single-cell retrieval device (CytePicker™) for whole genome amplification and subsequent analysis by PCR and Sanger sequencing, whole exome sequencing, or array-based comparative genomic hybridization. Clinical CTCs were evaluated in blood samples from patients with different cancers in comparison with the CellSearch® system.
AccuCyte--CyteFinder presented high-resolution images that allowed identification of mCTCs by morphologic and phenotypic features. Spike-in mCTC recoveries were between 90 and 91%. More than 80% of single-digit spike-in mCTCs were identified and even a single cell in 7.5 mL could be found. Analysis of single SKBR3 mCTCs identified presence of a known TP53 mutation by both PCR and whole exome sequencing, and confirmed the reported karyotype of this cell line. Patient sample CTC counts matched or exceeded CellSearch CTC counts in a small feasibility cohort.
The AccuCyte--CyteFinder system is a comprehensive and sensitive platform for identification and characterization of CTCs that has been applied to the assessment of CTCs in cancer patient samples as well as the isolation of single cells for genomic analysis. It thus enables accurate non-invasive monitoring of CTCs and evolving cancer biology for personalized, molecularly-guided cancer treatment.
循环肿瘤细胞(CTC)是从实体癌迁移至血液中的恶性细胞,通常数量稀少。人们对利用CTC来监测治疗反应、识别具有临床可操作性的生物标志物以及提供肿瘤分子状态的非侵入性窗口有着浓厚兴趣。在此,我们对AccuCyte®--CyteFinder®系统的性能进行了表征,该系统是一个全面、可重复且高度灵敏的平台,用于在对上皮标志物进行自动免疫荧光染色后,从显微镜载玻片上收集、识别和检索单个CTC以进行分子分析。
所有实验均采用基于密度的细胞分离装置(AccuCyte)从血液中分离有核细胞,并将其转移至显微镜载玻片上。染色后,使用数字扫描显微镜(CyteFinder)对载玻片进行成像。将来自四种癌细胞系的精确计数的模型CTC(mCTC)加入全血中以确定回收率。使用单细胞检索装置(CytePicker™)从载玻片上移除单个mCTC,用于全基因组扩增,随后通过PCR和桑格测序、全外显子组测序或基于阵列的比较基因组杂交进行分析。与CellSearch®系统相比,对来自不同癌症患者的血样中的临床CTC进行了评估。
AccuCyte--CyteFinder呈现出高分辨率图像,能够通过形态学和表型特征识别mCTC。加入的mCTC回收率在90%至91%之间。超过80%的个位数加入的mCTC被识别出来,甚至在7.5 mL血液中单个细胞也能被找到。对单个SKBR3 mCTC的分析通过PCR和全外显子组测序均鉴定出已知的TP53突变,并证实了该细胞系报道的核型。在一个小型可行性队列中,患者样本的CTC计数与CellSearch CTC计数匹配或超过后者。
AccuCyte--CyteFinder系统是一个用于识别和表征CTC的全面且灵敏的平台,已应用于癌症患者样本中CTC的评估以及单细胞分离以进行基因组分析。因此,它能够对CTC进行准确的非侵入性监测,并为个性化的分子导向癌症治疗监测不断演变的癌症生物学特性。