The Parsortix™ Cell Separation System-A versatile liquid biopsy platform

被引:129
作者
Miller, M. Craig [1 ]
Robinson, Peggy S. [2 ]
Wagner, Christopher [3 ]
O'Shannessy, Daniel J. [4 ]
机构
[1] ANGLE North Amer Inc, Clin Dev, King Of Prussia, PA USA
[2] ANGLE North Amer Inc, Corp, King Of Prussia, PA USA
[3] ANGLE North Amer Inc, Commercial Operat, King Of Prussia, PA USA
[4] ANGLE North Amer Inc, Res & Dev, King Of Prussia, PA USA
关键词
liquid biopsy; circulating tumor cell; microfluidics; rare cell isolation; CIRCULATING TUMOR-CELLS;
D O I
10.1002/cyto.a.23571
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Cancer cells from solid tumors can enter the circulatory system and survive to subsequently form distant metastases. The CellSearch (R) system (Menarini-Silicon Biosystems, Huntingdon Valley, PA) was the first, FDA-cleared system that provided a reliable tool for the investigation of circulating tumor cells (CTCs), which have been shown to be strongly associated with poor survival and therapy failure. Since that time, a number of new technologies have been introduced to improve CTC detection and/or isolation for further characterization. The continued and growing interest in the "liquid biopsy" field has spurred the development of numerous different CTC technologies. However, selecting the most appropriate CTC platform for individual applications can be challenging. No consensus has yet been reached in the community regarding which liquid biopsy technology is optimal. Here, we introduce the Parsortix (TM) Cell Separation System (ANGLE North America, Inc., King of Prussia, PA), a microfluidic based technology that captures rare cells based on size and deformability, offers reproducibly high capture efficiency, and produces highly enriched, viable (viability dependent on preservative used) CTCs that are amenable to a multitude of downstream analyses, including the isolation and interrogation of single cells. (c) 2018 The Authors. Cytometry Part A published by Wiley Periodicals, Inc. on behalf of International Society for Advancement of Cytometry.
引用
收藏
页码:1234 / 1239
页数:6
相关论文
共 13 条
[1]   Clinical evaluation of a novel microfluidic device for epitope-independent enrichment of circulating tumour cells in patients with small cell lung cancer [J].
Chudziak, Jakub ;
Burt, Deborah J. ;
Mohan, Sumitra ;
Rothwell, Dominic G. ;
Mesquita, Barbara ;
Antonello, Jenny ;
Dalby, Suzanne ;
Ayub, Mahmood ;
Priest, Lynsey ;
Carter, Louise ;
Krebs, Matthew G. ;
Blackhall, Fiona ;
Dive, Caroline ;
Brady, Ged .
ANALYST, 2016, 141 (02) :669-678
[2]   Filter Characteristics Influencing Circulating Tumor Cell Enrichment from Whole Blood [J].
Coumans, Frank A. W. ;
van Dalum, Guus ;
Beck, Markus ;
Terstappen, Leon W. M. M. .
PLOS ONE, 2013, 8 (04)
[3]   In Situ Detection and Quantification of AR-V7, AR-FL, PSA, and KRAS Point Mutations in Circulating Tumor Cells [J].
El-Heliebi, Amin ;
Hille, Claudia ;
Laxman, Navya ;
Svedlund, Jessica ;
Haudum, Christoph ;
Ercan, Erkan ;
Kroneis, Thomas ;
Chen, Shukun ;
Smolle, Maria ;
Rossmann, Christopher ;
Krzywkowski, Tomasz ;
Ahlford, Annika ;
Darai, Evangelia ;
von Amsberg, Gunhild ;
Alsdorf, Winfried ;
Koenig, Frank ;
Loehr, Matthias ;
de Kruijff, Inge ;
Riethdorf, Sabine ;
Gorges, Tobias M. ;
Pantel, Klaus ;
Bauernhofer, Thomas ;
Nilsson, Mats ;
Sedlmayr, Peter .
CLINICAL CHEMISTRY, 2018, 64 (03) :536-546
[4]   Accession of Tumor Heterogeneity by Multiplex Transcriptome Profiling of Single Circulating Tumor Cells [J].
Gorges, Tobias M. ;
Kuske, Andra ;
Roeck, Katharina ;
Mauermann, Oliver ;
Mueller, Volkmar ;
Peine, Sven ;
Verpoort, Karl ;
Novosadova, Vendula ;
Kubista, Mikael ;
Riethdorf, Sabine ;
Pantel, Klaus .
CLINICAL CHEMISTRY, 2016, 62 (11) :1504-1515
[5]   A novel microfluidic platform for size and deformability based separation and the subsequent molecular characterization of viable circulating tumor cells [J].
Hvichia, G. E. ;
Parveen, Z. ;
Wagner, C. ;
Janning, M. ;
Quidde, J. ;
Stein, A. ;
Mueller, V. ;
Loges, S. ;
Neves, R. P. L. ;
Stoecklein, N. H. ;
Wikman, H. ;
Riethdorf, S. ;
Pantel, K. ;
Gorges, T. M. .
INTERNATIONAL JOURNAL OF CANCER, 2016, 138 (12) :2894-2904
[6]   Circulating Tumor Cell Analysis in Preclinical Mouse Models of Metastasis [J].
Kitz, Jenna ;
Lowes, Lori E. ;
Goodale, David ;
Allan, Alison L. .
DIAGNOSTICS, 2018, 8 (02)
[7]   A Novel Workflow to Enrich and Isolate Patient-Matched EpCAMhigh and EpCAMlow/negative CTCs Enables the Comparative Characterization of the PIK3CA Status in Metastatic Breast Cancer [J].
Lampignano, Rita ;
Yang, Liwen ;
Neumann, Martin H. D. ;
Franken, Andre ;
Fehm, Tanja ;
Niederacher, Dieter ;
Neubauer, Hans .
INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 2017, 18 (09)
[8]   Comparison of isolation platforms for detection of circulating renal cell carcinoma cells [J].
Maertens, Yvonne ;
Humberg, Verena ;
Erlmeier, Franziska ;
Steffens, Sandra ;
Steinestel, Julie ;
Boegemann, Martin ;
Schrader, Andres Jan ;
Bernemann, Christof .
ONCOTARGET, 2017, 8 (50) :87710-87717
[9]   The precious cell block [J].
Mayall, Frederick George ;
Bodger, Ian ;
Pepperell, Justin ;
Stevanato, Lara ;
Hustler, Arianna ;
Mumford, Kyra Mhairi .
JOURNAL OF CLINICAL PATHOLOGY, 2018, 71 (07) :659-+
[10]   Efficient leukocyte depletion by a novel microfluidic platform enables the molecular detection and characterization of circulating tumor cells [J].
Obermayr, Eva ;
Maritschnegg, Elisabeth ;
Agreiter, Christiane ;
Pecha, Nina ;
Speiser, Paul ;
Helmy-Bader, Samir ;
Danzinger, Sabine ;
Krainer, Michael ;
Singer, Christian ;
Zeillinger, Robert .
ONCOTARGET, 2018, 9 (01) :812-823