Comparison of cell stabilizing blood collection tubes for circulating plasma tumor DNA

被引:83
作者
Toro, Patricia Valda [1 ]
Erlanger, Bracha [1 ]
Beaver, Julia A. [1 ]
Cochran, Rory L. [1 ]
VanDenBerg, Dustin A. [1 ]
Yakim, Elizabeth [1 ]
Cravero, Karen [1 ]
Chu, David [1 ]
Zabransky, Daniel J. [1 ]
Wong, Hong Yuen [1 ]
Croessmann, Sarah [1 ]
Parsons, Heather [1 ]
Hurley, Paula J. [1 ,2 ]
Lauring, Josh [1 ]
Park, Ben Ho [1 ,3 ]
机构
[1] Johns Hopkins Univ, Sidney Kimmel Comprehens Canc Ctr, Sch Med, Baltimore, MD 21287 USA
[2] Brady Urol Inst, Dept Urol, Baltimore, MD USA
[3] Johns Hopkins Univ, Dept Chem & Biomol Engn, Whiting Sch Engn, Baltimore, MD 21287 USA
关键词
Droplet digital PCR; Circulating tumor DNA; Plasma tumor DNA; Cell stabilizing tube; METASTATIC BREAST-CANCER; MATERNAL PLASMA; DIGITAL PCR; FETAL DNA; REAGENT; STORAGE;
D O I
10.1016/j.clinbiochem.2015.07.097
中图分类号
R446 [实验室诊断]; R-33 [实验医学、医学实验];
学科分类号
1001 ;
摘要
Objectives: Circulating plasma DNA is being increasingly used for biomedical and clinical research as a substrate for genetic testing. However, cell lysis can occur hours after venipuncture when using standard tubes for blood collection, leading to an increase in contaminating cellular DNA that may hinder analysis of circulating plasma DNA. Cell stabilization agents can prevent cellular lysis for several days, reducing the need for immediate plasma preparation after venipuncture, thereby facilitating the ease of blood collection and sample preparation for clinical research. However, the majority of cell stabilizing reagents have not been formally tested for their ability to preserve circulating plasma tumor DNA. Design & methods: In this study, we compared the properties of two cell stabilizing reagents, the cell-free DNA BCT tube and the PAXgene tube, by collecting blood samples from metastatic breast cancer patients and measuring genome equivalents of plasma DNA by droplet digital PCR. We compared wild type PIK3CA genome equivalents and also assayed for two PIK3C4 hotspot mutations, E545K and H1047R. Results: Our results demonstrate that blood stored for 7 days in BCT tubes did not show evidence of cell lysis, whereas PAXgene tubes showed an order of magnitude increase in genome equivalents, indicative of considerable cellular lysis. Conclusions: We conclude that BCT tubes can prevent lysis and cellular release of genomic DNA of blood samples from cancer patients when stored at room temperature, and could therefore be of benefit for blood specimen collections in clinical trials. (C) 2015 The Canadian Society of Clinical Chemists. Published by Elsevier Inc. All rights reserved.
引用
收藏
页码:993 / 998
页数:6
相关论文
共 14 条
[1]   Detection of Cancer DNA in Plasma of Patients with Early-Stage Breast Cancer [J].
Beaver, Julia A. ;
Jelovac, Danijela ;
Balukrishna, Sasidharan ;
Cochran, Rory L. ;
Croessmann, Sarah ;
Zabransky, Daniel J. ;
Wong, Hong Yuen ;
Toro, Patricia Valda ;
Cidado, Justin ;
Blair, Brian G. ;
Chu, David ;
Burns, Timothy ;
Higgins, Michaela J. ;
Stearns, Vered ;
Jacobs, Lisa ;
Habibi, Mehran ;
Lange, Julie ;
Hurley, Paula J. ;
Lauring, Josh ;
VanDenBerg, Dustin A. ;
Kessler, Jill ;
Jeter, Stacie ;
Samuels, Michael L. ;
Maar, Dianna ;
Cope, Leslie ;
Cimino-Mathews, Ashley ;
Argani, Pedram ;
Wolff, Antonio C. ;
Park, Ben Ho .
CLINICAL CANCER RESEARCH, 2014, 20 (10) :2643-2650
[2]   Circulating tumor cells, disease progression, and survival in metastatic breast cancer [J].
Cristofanilli, M ;
Budd, GT ;
Ellis, MJ ;
Stopeck, A ;
Matera, J ;
Miller, MC ;
Reuben, JM ;
Doyle, GV ;
Allard, WJ ;
Terstappen, LWMM ;
Hayes, DF .
NEW ENGLAND JOURNAL OF MEDICINE, 2004, 351 (08) :781-791
[3]   Liquid biopsy: monitoring cancer-genetics in the blood [J].
Crowley, Emily ;
Di Nicolantonio, Federica ;
Loupakis, Fotios ;
Bardelli, Alberto .
NATURE REVIEWS CLINICAL ONCOLOGY, 2013, 10 (08) :472-484
[4]   Effects of a novel cell stabilizing reagent on DNA amplification by PCR as compared to traditional stabilizing reagents [J].
Das, Kausik ;
Fernando, M. Rohan ;
Basiaga, Sara ;
Wigginton, Stephanie M. ;
Williams, Tom .
ACTA HISTOCHEMICA, 2014, 116 (01) :55-60
[5]   Circulating mutant DNA to assess tumor dynamics [J].
Diehl, Frank ;
Schmidt, Kerstin ;
Choti, Michael A. ;
Romans, Katharine ;
Goodman, Steven ;
Li, Meng ;
Thornton, Katherine ;
Agrawal, Nishant ;
Sokoll, Lori ;
Szabo, Steve A. ;
Kinzler, Kenneth W. ;
Vogelstein, Bert ;
Diaz, Luis A., Jr. .
NATURE MEDICINE, 2008, 14 (09) :985-990
[6]   A new methodology to preserve the original proportion and integrity of cell-free fetal DNA in maternal plasma during sample processing and storage [J].
Fernando, M. R. ;
Chen, K. ;
Norton, S. ;
Krzyzanowski, G. ;
Bourne, D. ;
Hunsley, B. ;
Ryan, W. L. ;
Bassett, C. .
PRENATAL DIAGNOSIS, 2010, 30 (05) :418-424
[7]   Establishment of tumor-specific copy number alterations from plasma DNA of patients with cancer [J].
Heitzer, Ellen ;
Auer, Martina ;
Hoffmann, Eva Maria ;
Pichler, Martin ;
Gasch, Christin ;
Ulz, Peter ;
Lax, Sigurd ;
Waldispuehl-Geigl, Julie ;
Mauermann, Oliver ;
Mohan, Sumitra ;
Pristauz, Gunda ;
Lackner, Carolin ;
Hoefler, Gerald ;
Eisner, Florian ;
Petru, Edgar ;
Sill, Heinz ;
Samonigg, Hellmut ;
Pantel, Klaus ;
Riethdorf, Sabine ;
Bauernhofer, Thomas ;
Geigl, Jochen B. ;
Speicher, Michael R. .
INTERNATIONAL JOURNAL OF CANCER, 2013, 133 (02) :346-356
[8]   Detection of Tumor PIK3CA Status in Metastatic Breast Cancer Using Peripheral Blood [J].
Higgins, Michaela J. ;
Jelovac, Danijela ;
Barnathan, Evan ;
Blair, Brian ;
Slater, Shannon ;
Powers, Penny ;
Zorzi, Jane ;
Jeter, Stacie C. ;
Oliver, George R. ;
Fetting, John ;
Emens, Leisha ;
Riley, Carol ;
Stearns, Vered ;
Diehl, Frank ;
Angenendt, Philipp ;
Huang, Peng ;
Cope, Leslie ;
Argani, Pedram ;
Murphy, Kathleen M. ;
Bachman, Kurtis E. ;
Greshock, Joel ;
Wolff, Antonio C. ;
Park, Ben H. .
CLINICAL CANCER RESEARCH, 2012, 18 (12) :3462-3469
[9]   Absolute quantification by droplet digital PCR versus analog real-time PCR [J].
Hindson, Christopher M. ;
Chevillet, John R. ;
Briggs, Hilary A. ;
Gallichotte, Emily N. ;
Ruf, Ingrid K. ;
Hindson, Benjamin J. ;
Vessella, Robert L. ;
Tewari, Muneesh .
NATURE METHODS, 2013, 10 (10) :1003-+
[10]   Quantitative analysis of fetal DNA in maternal plasma and serum: Implications for noninvasive prenatal diagnosis [J].
Lo, YMD ;
Tein, MSC ;
Lau, TK ;
Haines, CJ ;
Leung, TN ;
Poon, PMK ;
Wainscoat, JS ;
Johnson, PJ ;
Chang, AMZ ;
Hjelm, NM .
AMERICAN JOURNAL OF HUMAN GENETICS, 1998, 62 (04) :768-775