Self-Seeding Microwells to Isolate and Assess the Viability of Single Circulating Tumor Cells

被引:11
作者
Andree, Kiki C. [1 ]
Abali, Fikri [1 ]
Oomens, Lisa [2 ]
Passanha, Fiona R. [1 ]
Broekmaat, Joska J. [2 ]
Kraan, Jaco [3 ,4 ]
Mendelaar, Pauline A. J. [3 ,4 ]
Sleijfer, Stefan [3 ,4 ]
Terstappen, Leon W. M. M. [1 ]
机构
[1] Univ Twente, Med Cell BioPhys, Hallenweg 23, NL-7522 NH Enschede, Netherlands
[2] VyCAP BV, Abraham Rademakerstr 41, NL-7425 PG Deventer, Netherlands
[3] Erasmus MC, Dept Med Oncol, Inst Canc, Dr Molewaterpl 40, NL-3015 GD Rotterdam, Netherlands
[4] Canc Genom Netherlands, Dr Molewaterpl 40, NL-3015 GD Rotterdam, Netherlands
来源
INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES | 2019年 / 20卷 / 03期
关键词
CTC; self-seeding microwells; single cell isolation; breast cancer; prostate cancer; CANCER; ENRICHMENT; APOPTOSIS; SYSTEM; EXPRESSION; CULTURE; BLOOD;
D O I
10.3390/ijms20030477
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The availability of viable tumor cells could significantly improve the disease management of cancer patients. Here we developed and evaluated a method using self-seeding microwells to obtain single circulating tumor cells (CTC) and assess their potential to expand. Conditions were optimized using cells from the breast cancer cell line MCF-7 and blood from healthy volunteers collected in EDTA blood collection tubes. 43% of the MCF-7 cells (nucleus+, Ethidium homodimer-1-, Calcein AM+, -EpCAM+, -CD45-) spiked into 7.5 mL of blood could be recovered with 67% viability and these could be further expanded. The same procedure tested in metastatic breast and prostate cancer patients resulted in a CTC recovery of only 0-5% as compared with CTC counts obtained with the CellSearch((R)) system. Viability of the detected CTC ranged from 0-36%. Cell losses could be mainly contributed to the smaller size and greater flexibility of CTC as compared to cultured cells from cell lines and loss during leukocyte depletion prior to cell seeding. Although CTC losses can be reduced by fixation, to obtain viable CTC no fixatives can be used and pore size in the bottom of microwells will need to be reduced, filtration conditions adapted and pre-enrichment improved to reduce CTC losses.
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页数:13
相关论文
共 38 条
  • [11] Tumor Heterogeneity: Mechanisms and Bases for a Reliable Application of Molecular Marker Design
    Diaz-Cano, Salvador J.
    [J]. INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 2012, 13 (02): : 1951 - 2011
  • [12] Organoid culture systems for prostate epithelial and cancer tissue
    Drost, Jarno
    Karthaus, Wouter R.
    Gao, Dong
    Driehuis, Else
    Sawyers, Charles L.
    Chen, Yu
    Clevers, Hans
    [J]. NATURE PROTOCOLS, 2016, 11 (02) : 347 - 358
  • [13] Organoids as an in vitro model of human development and disease
    Fatehullah, Aliya
    Tan, Si Hui
    Barker, Nick
    [J]. NATURE CELL BIOLOGY, 2016, 18 (03) : 246 - 254
  • [14] Faugeroux V., 2017, P ACTC RHOD GREEC 4, P106
  • [15] Organoid Cultures Derived from Patients with Advanced Prostate Cancer
    Gao, Dong
    Vela, Ian
    Sboner, Andrea
    Iaquinta, Phillip J.
    Karthaus, Wouter R.
    Gopalan, Anuradha
    Dowling, Catherine
    Wanjala, Jackline N.
    Undvall, Eva A.
    Arora, Vivek K.
    Wongvipat, John
    Kossai, Myriam
    Ramazanoglu, Sinan
    Barboza, Luendreo P.
    Di, Wei
    Cao, Zhen
    Zhang, Qi Fan
    Sirota, Inna
    Ran, Leili
    MacDonald, Theresa Y.
    Beltran, Himisha
    Mosquera, Juan-Miguel
    Touijer, Karim A.
    Scardino, Peter T.
    Laudone, Vincent P.
    Curtis, Kristen R.
    Rathkopf, Dana E.
    Morris, Michael J.
    Danila, Daniel C.
    Slovin, Susan F.
    Solomon, Stephen B.
    Eastham, James A.
    Chi, Ping
    Carver, Brett
    Rubin, Mark A.
    Scher, Howard I.
    Clevers, Hans
    Sawyers, Charles L.
    Chen, Yu
    [J]. CELL, 2014, 159 (01) : 176 - 187
  • [16] The Evolving War on Cancer
    Haber, Daniel A.
    Gray, Nathanael S.
    Baselga, Jose
    [J]. CELL, 2011, 145 (01) : 19 - 24
  • [17] Hallmarks of Cancer: The Next Generation
    Hanahan, Douglas
    Weinberg, Robert A.
    [J]. CELL, 2011, 144 (05) : 646 - 674
  • [18] Circulating tumour cells in patients with urothelial tumours: Enrichment and in vitro culture
    Kolostova, Katarina
    Cegan, Martin
    Bobek, Vladimir
    [J]. CUAJ-CANADIAN UROLOGICAL ASSOCIATION JOURNAL, 2014, 8 (9-10): : E715 - E720
  • [19] Single-Cell Analyses of Prostate Cancer Liquid Biopsies Acquired by Apheresis
    Lambros, Maryou B.
    Seed, George
    Sumanasuriya, Semini
    Gil, Veronica
    Crespo, Mateus
    Fontes, Mariane
    Chandler, Rob
    Mehra, Niven
    Fowler, Gemma
    Ebbs, Berni
    Flohr, Penny
    Miranda, Susana
    Yuan, Wei
    Mackay, Alan
    Ferreira, Ana
    Pereira, Rita
    Bertan, Claudia
    Figueiredo, Ines
    Riisnaes, Ruth
    Rodrigues, Daniel Nava
    Sharp, Adam
    Goodall, Jane
    Boysen, Gunther
    Carreira, Suzanne
    Bianchini, Diletta
    Rescigno, Pasquale
    Zafeiriou, Zafeiris
    Hunt, Joanne
    Moloney, Deirdre
    Hamilton, Lucy
    Neves, Rui P.
    Swennenhuis, Joost
    Andree, Kiki
    Stoecklein, Nikolas H.
    Terstappen, Leon W. M. M.
    de Bono, Johann S.
    [J]. CLINICAL CANCER RESEARCH, 2018, 24 (22) : 5635 - 5644
  • [20] Apoptosis of circulating tumor cells in prostate cancer patients
    Larson, CJ
    Moreno, JG
    Pienta, KJ
    Gross, S
    Repollet, M
    O'Hara, SM
    Russell, T
    Terstappen, LWMM
    [J]. CYTOMETRY PART A, 2004, 62A (01) : 46 - 53