Antibody-independent capture of circulating tumor cells of non-epithelial origin with the ApoStream® system

被引:45
作者
Balasubramanian, Priya [1 ]
Kinders, Robert J. [1 ]
Kummar, Shivaani [2 ]
Gupta, Vishal [3 ]
Hasegawa, David [3 ]
Menachery, Anoop [3 ]
Lawrence, Scott M. [1 ]
Wang, Lihua [1 ]
Ferry-Galow, Katherine [1 ]
Davis, Darren [3 ]
Parchment, Ralph E. [1 ]
Tomaszewski, Joseph E. [2 ]
Doroshow, James H. [2 ]
机构
[1] Leidos Biomed Res Inc, Frederick Natl Lab Canc Res, Lab Human Toxicol & Pharmacol, Applied Dev Res Support Directorate, Frederick, MD 21701 USA
[2] NCI, Div Canc Treatment & Diag, Bethesda, MD 20892 USA
[3] ApoCell Inc, Houston, TX USA
来源
PLOS ONE | 2017年 / 12卷 / 04期
基金
美国国家卫生研究院;
关键词
SOFT PART SARCOMA; FIELD-FLOW FRACTIONATION; CANCER; DIELECTROPHORESIS; NEOPLASMS; SURVIVAL; BLOOD; TFE3; GENE; HEAD;
D O I
10.1371/journal.pone.0175414
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Circulating tumor cells (CTCs) are increasingly employed for research and clinical monitoring of cancer, though most current methods do not permit the isolation of non-epithelial tumor cells. Furthermore, CTCs isolated with antibody-dependent methods are not suitable for downstream experimental uses, including in vitro culturing and implantation in vivo. In the present study, we describe the development, validation, and transfer across laboratories of a new antibody-independent device for the enrichment of CTCs from blood samples of patients with various cancer diagnoses. The ApoStream (R) device uses dielectrophoresis (DEP) field-flow assist to separate non-hematopoietic cells from the peripheral blood mononuclear fraction by exposing cells in a laminar flow stream to a critical alternating current frequency. The ApoStream (R) device was calibrated and validated in a formal cross-laboratory protocol using 3 different cancer cell lines spanning a range of distinct phenotypes (A549, MDA-MB-231, and ASPS-1). In spike-recovery experiments, cancer cell recovery efficiencies appeared independent of spiking level and averaged between 68% and 55%, depending on the cell line. No inter-run carryover was detected in control samples. Moreover, the clinical-readiness of the device in the context of non-epithelial cancers was evaluated with blood specimens from fifteen patients with metastatic sarcoma. The ApoStream (R) device successfully isolated CTCs from all patients with sarcomas examined, and the phenotypic heterogeneity of the enriched cells was demonstrated by fluorescence in situ hybridization or with multiplex immunophenotyping panels. Therefore, the ApoStream (R) technology expands the clinical utility of CTC evaluation to mesenchymal cancers.
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页数:15
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