Sonnenberg Avery, Marciniak Jennifer Y, Skowronski Elaine A, Manouchehri Sareh, Rassenti Laura, Ghia Emanuela M, Widhopf George F, Kipps Thomas J, Heller Michael J
Department of Bioengineering, University of California San Diego, La Jolla, CA, USA.
Electrophoresis. 2014 Jul;35(12-13):1828-36. doi: 10.1002/elps.201400016. Epub 2014 May 14.
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).
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。