Detection of tumor-associated cells in cryopreserved peripheral blood mononuclear cell samples for retrospective analysis

被引:15
作者
Zhu, Peixuan [1 ]
Stanton, Melissa L. [2 ]
Castle, Erik P. [3 ]
Joseph, Richard W. [4 ]
Adams, Daniel L. [1 ]
Li, Shuhong [1 ]
Amstutz, Platte [1 ]
Tang, Cha-Mei [1 ]
Ho, Thai H. [5 ]
机构
[1] Creatv MicroTech Inc, 11609 Lake Potomac Dr, Potomac, MD 20854 USA
[2] Mayo Clin, Dept Lab Med & Pathol, 13400 East Shea Blvd, Scottsdale, AZ 85259 USA
[3] Mayo Clin Hosp, Dept Urol, 5777 E Mayo Blvd, Phoenix, AZ 85054 USA
[4] Mayo Clin, Div Hematol & Med Oncol, 4500 San Pablo Rd, Jacksonville, FL 32224 USA
[5] Mayo Clin, Div Hematol & Med Oncol, 13400 East Shea Blvd, Scottsdale, AZ 85259 USA
来源
JOURNAL OF TRANSLATIONAL MEDICINE | 2016年 / 14卷
基金
美国国家卫生研究院;
关键词
Circulating cancer-associated macrophage-like cells (CAMLs); CellSieve (TM) microfiltration; Cryopreservation; Circulating tumor cells (CTCs); Ficoll; Fluorescence antibody staining; CANCER; MICROFILTER; PROGRESSION; SURVIVAL; SIZE;
D O I
10.1186/s12967-016-0953-2
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Background: Cryopreserved peripheral blood mononuclear cells (PBMCs) are commonly collected in biobanks. However, little data exist regarding the preservation of tumor-associated cells in cryopreserved collections. The objective of this study was to determine the feasibility of using the CellSieve (TM) microfiltration assay for the isolation of circulating tumor cells (CTCs) and circulating cancer-associated macrophage-like cells (CAMLs) from cryopreserved PBMC samples. Methods: Blood samples spiked with breast (MCF-7), prostate (PC-3), and renal (786-O) cancer cell lines were used to establish analytical accuracy, efficiency, and reproducibility after cryopreservation. The spiked samples were processed through Ficoll separation, and cryopreservation was followed by thawing and microfiltration. Results: MCF-7 cells were successfully retrieved with recovery efficiencies of 90.5 % without cryopreservation and 87.8 and 89.0 %, respectively, on day 7 and day 66 following cryopreservation. The corresponding recovery efficiencies of PC-3 cells were 83.3 % without cryopreservation and 85.3 and 84.7 %, respectively, after cryopreservation. Recovery efficiencies of 786-O cells were 92.7 % without cryopreservation, and 82.7 and 81.3 %, respectively, after cryopreservation. The recovered cells retained the morphologic characteristics and immunohistochemical markers that had been observed before freezing. The protocols were further validated by quantitation of CAMLs in blood samples from two patients with renal cell carcinoma (RCC). The recovery rates of CTCs and CAMLs from cryopreserved samples were not statistically significant different (P > 0.05) from matched fresh samples. Conclusions: To our knowledge, this is the first report that CAMLs could be cryopreserved and analyzed after thawing with microfiltration technology. The application of microfiltration technology to cryopreserved samples will enable much greater retrospective study of cancer patients in relation to long-term outcomes.
引用
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页数:12
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