Label-free enrichment of rare unconventional circulating neoplastic cells using a microfluidic dielectrophoretic sorting device

被引:13
作者
Mira, Jose Montoya [1 ,2 ]
Sapre, Ajay A. [1 ]
Walker, Brett S. [3 ]
Alvarez, Jesus Bueno [1 ]
Gustafson, Kyle T. [1 ,2 ]
Tu, Eugene [1 ]
Fischer, Jared M. [1 ,4 ,5 ]
Wong, Melissa H. [4 ,6 ]
Esener, Sadik [1 ,2 ,4 ]
Chiu, Yu-Jui [1 ]
机构
[1] Oregon Hlth & Sci Univ, Knight Canc Early Detect Adv Res Ctr, Portland, OR 97201 USA
[2] Oregon Hlth & Sci Univ, Dept Biomed Engn, Portland, OR 97201 USA
[3] Oregon Hlth & Sci Univ, Dept Surg, Portland, OR 97239 USA
[4] Oregon Hlth & Sci Univ, Knight Canc Inst, Portland, OR 97201 USA
[5] Oregon Hlth & Sci Univ, Dept Mol & Med Genet, Portland, OR 97239 USA
[6] Oregon Hlth & Sci Univ, Dept Cell Dev & Canc Biol, Portland, OR 97201 USA
关键词
TUMOR-CELLS; CANCER-CELLS; SEPARATION; KRAS;
D O I
10.1038/s42003-021-02651-8
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Cellular circulating biomarkers from the primary tumor such as circulating tumor cells (CTCs) and circulating hybrid cells (CHCs) have been described to harbor tumor-like phenotype and genotype. CHCs are present in higher numbers than CTCs supporting their translational potential. Methods for isolation of CHCs do not exist and are restricted to low-throughput, time consuming, and biased methodologies. We report the development of a label-free dielectrophoretic microfluidic platform facilitating enrichment of CHCs in a high-throughput and rapid fashion by depleting healthy peripheral blood mononuclear cells (PBMCs). We demonstrated up to 96.5% depletion of PBMCs resulting in 18.6-fold enrichment of cancer cells. In PBMCs from pancreatic adenocarcinoma patients, the platform enriched neoplastic cells identified by their KRAS mutant status using droplet digital PCR with one hour of processing. Enrichment was achieved in 75% of the clinical samples analyzed, establishing this approach as a promising way to non-invasively analyze tumor cells from patients. Montoya Mira & Sapre et al. design a microfluidic device utilizing dielectrophoresis for the enrichment of circulating neoplastic cells that possess both epithelial and immune-like characteristics. They optimized the device using in vitro models and then applied it to clinical samples for clinically relevant mutation analyses.
引用
收藏
页数:9
相关论文
共 56 条
[1]   Dielectrophoresis for Biomedical Sciences Applications: A Review [J].
Abd Rahman, Nurhaslina ;
Ibrahim, Fatimah ;
Yafouz, Bashar .
SENSORS, 2017, 17 (03)
[2]   Dielectric Characterization and Separation Optimization of Infiltrating Ductal Adenocarcinoma via Insulator-Dielectrophoresis [J].
Adekanmbi, Ezekiel O. ;
Giduthuri, Anthony T. ;
Srivastava, Soumya K. .
MICROMACHINES, 2020, 11 (04)
[3]   Activated Kras and Ink4a/Arf deficiency cooperate to produce metastatic pancreatic ductal adenocarcinoma [J].
Aguirre, AJ ;
Bardeesy, N ;
Sinha, M ;
Lopez, L ;
Tuveson, DA ;
Horner, J ;
Redston, MS ;
DePinho, RA .
GENES & DEVELOPMENT, 2003, 17 (24) :3112-3126
[4]   MOST HUMAN CARCINOMAS OF THE EXOCRINE PANCREAS CONTAIN MUTANT C-K-RAS GENES [J].
ALMOGUERA, C ;
SHIBATA, D ;
FORRESTER, K ;
MARTIN, J ;
ARNHEIM, N ;
PERUCHO, M .
CELL, 1988, 53 (04) :549-554
[5]   Circulating tumour cells as a biomarker for diagnosis and staging in pancreatic cancer [J].
Ankeny, J. S. ;
Court, C. M. ;
Hou, S. ;
Li, Q. ;
Song, M. ;
Wu, D. ;
Chen, J. F. ;
Lee, T. ;
Lin, M. ;
Sho, S. ;
Rochefort, M. M. ;
Girgis, M. D. ;
Yao, J. ;
Wainberg, Z. A. ;
Muthusamy, V. R. ;
Watson, R. R. ;
Donahue, T. R. ;
Hines, O. J. ;
Reber, H. A. ;
Graeber, T. G. ;
Tseng, H. R. ;
Tomlinson, J. S. .
BRITISH JOURNAL OF CANCER, 2016, 114 (12) :1367-1375
[6]   Tumor stem cells fuse with monocytes to form highly invasive tumor-hybrid cells [J].
Augusto Aguirre, Luis ;
Montalban-Hernandez, Karla ;
Avendano-Ortiz, Jose ;
Marin, Elvira ;
Lozano, Roberto ;
Toledano, Victor ;
Sanchez-Maroto, Laura ;
Terron, Veronica ;
Valentin, Jaime ;
Pulido, Elisa ;
Carlos Casalvilla, Jose ;
Rubio, Carolina ;
Diekhorst, Luke ;
Laso-Garcia, Fernando ;
del Fresno, Carlos ;
Collazo-Lorduy, Ana ;
Jimenez-Munarriz, Beatriz ;
Gomez-Campelo, Paloma ;
Llanos-Gonzalez, Emilio ;
Fernandez-Velasco, Maria ;
Rodriguez-Antolin, Carlos ;
Perez de Diego, Rebeca ;
Cantero-Cid, Ramon ;
Hernadez-Jimenez, Enrique ;
Alvarez, Enrique ;
Rosas, Rocio ;
Dies Lopez-Ayllon, Blanca ;
de Castro, Javier ;
Wculek, Stefanie K. ;
Cubillos-Zapata, Carolina ;
Ibanez de Caceres, Inmaculada ;
Diaz-Agero, Prudencio ;
Gutierrez Fernandez, Maria ;
Paz de Miguel, Maria ;
Sancho, David ;
Schulte, Leon ;
Perona, Rosario ;
Belda-Iniesta, Cristobal ;
Bosca, Lisardo ;
Lopez-Collazo, Eduardo .
ONCOIMMUNOLOGY, 2020, 9 (01)
[7]   Nanofluidic Digital PCR for KRAS Mutation Detection and Quantification in Gastrointestinal Cancer [J].
Azuara, Daniel ;
Ginesta, Mireia M. ;
Gausachs, Mireia ;
Rodriguez-Moranta, Francisco ;
Fabregat, Joan ;
Busquets, Juli ;
Pelaez, Nuria ;
Boadas, Jaume ;
Galter, Sara ;
Moreno, Victor ;
Costa, Jose ;
de Oca, Javier ;
Capella, Gabriel .
CLINICAL CHEMISTRY, 2012, 58 (09) :1332-1341
[8]   Antibody-independent capture of circulating tumor cells of non-epithelial origin with the ApoStream® system [J].
Balasubramanian, Priya ;
Kinders, Robert J. ;
Kummar, Shivaani ;
Gupta, Vishal ;
Hasegawa, David ;
Menachery, Anoop ;
Lawrence, Scott M. ;
Wang, Lihua ;
Ferry-Galow, Katherine ;
Davis, Darren ;
Parchment, Ralph E. ;
Tomaszewski, Joseph E. ;
Doroshow, James H. .
PLOS ONE, 2017, 12 (04)
[9]   Technologies for circulating tumor cell separation from whole blood [J].
Banko, Petra ;
Lee, Sun Young ;
Nagygyorgy, Viola ;
Zrinyi, Miklos ;
Chae, Chang Hoon ;
Cho, Dong Hyu ;
Telekes, Andras .
JOURNAL OF HEMATOLOGY & ONCOLOGY, 2019, 12 (1)
[10]   SEPARATION OF HUMAN BREAST-CANCER CELLS FROM BLOOD BY DIFFERENTIAL DIELECTRIC AFFINITY [J].
BECKER, FF ;
WANG, XB ;
HUANG, Y ;
PETHIG, R ;
VYKOUKAL, J ;
GASCOYNE, PRC .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1995, 92 (03) :860-864