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基于介电电泳从血液和血浆中分离并检测癌症相关循环游离DNA生物标志物

Dielectrophoretic isolation and detection of cancer-related circulating cell-free DNA biomarkers from blood and plasma.

作者信息

Sonnenberg Avery, Marciniak Jennifer Y, Skowronski Elaine A, Manouchehri Sareh, Rassenti Laura, Ghia Emanuela M, Widhopf George F, Kipps Thomas J, Heller Michael J

机构信息

Department of Bioengineering, University of California San Diego, La Jolla, CA, USA.

出版信息

Electrophoresis. 2014 Jul;35(12-13):1828-36. doi: 10.1002/elps.201400016. Epub 2014 May 14.

Abstract

Conventional methods for the isolation of cancer-related circulating cell-free (ccf) DNA from patient blood (plasma) are time consuming and laborious. A DEP approach utilizing a microarray device now allows rapid isolation of ccf-DNA directly from a small volume of unprocessed blood. In this study, the DEP device is used to compare the ccf-DNA isolated directly from whole blood and plasma from 11 chronic lymphocytic leukemia (CLL) patients and one normal individual. Ccf-DNA from both blood and plasma samples was separated into DEP high-field regions, after which cells (blood), proteins, and other biomolecules were removed by a fluidic wash. The concentrated ccf-DNA was detected on-chip by fluorescence, and then eluted for PCR and DNA sequencing. The complete process from blood to PCR required less than 10 min; an additional 15 min was required to obtain plasma from whole blood. Ccf-DNA from the equivalent of 5 μL of CLL blood and 5 μL of plasma was amplified by PCR using Ig heavy-chain variable (IGHV) specific primers to identify the unique IGHV gene expressed by the leukemic B-cell clone. The PCR and DNA sequencing results obtained by DEP from all 11 CLL blood samples and from 8 of the 11 CLL plasma samples were exactly comparable to the DNA sequencing results obtained from genomic DNA isolated from CLL patient leukemic B cells (gold standard).

摘要

从患者血液(血浆)中分离癌症相关循环游离(ccf)DNA的传统方法既耗时又费力。一种利用微阵列设备的DEP方法现在可以直接从小体积未处理血液中快速分离ccf-DNA。在本研究中,DEP设备用于比较从11例慢性淋巴细胞白血病(CLL)患者和1名正常个体的全血和血浆中直接分离的ccf-DNA。来自血液和血浆样本的ccf-DNA被分离到DEP高场区,之后通过流体冲洗去除细胞(血液)、蛋白质和其他生物分子。通过荧光在芯片上检测浓缩的ccf-DNA,然后洗脱用于PCR和DNA测序。从血液到PCR的整个过程耗时不到10分钟;从全血中获得血浆还需要额外15分钟。使用Ig重链可变区(IGHV)特异性引物通过PCR扩增相当于5μL CLL血液和5μL血浆中的ccf-DNA,以鉴定白血病B细胞克隆表达的独特IGHV基因。通过DEP从所有11例CLL血液样本和11例CLL血浆样本中的8例获得的PCR和DNA测序结果与从CLL患者白血病B细胞中分离的基因组DNA(金标准)获得的DNA测序结果完全可比。

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