Development and Validation of Multiplex Liquid Bead Array Assay for the Simultaneous Expression of 14 Genes in Circulating Tumor Cells

被引:4
|
作者
Parisi, Cleo [1 ]
Markou, Athina [1 ]
Strati, Areti [1 ]
Kasimir-Bauer, Sabine [2 ]
Lianidou, Evi S. [1 ]
机构
[1] Univ Athens, Dept Chem, Lab Analyt Chem, Anal Circulating Tumor Cells Lab, GR-15771 Athens, Greece
[2] Univ Duisburg Essen, Univ Hosp Essen, Dept Gynecol & Obstet, D-45122 Essen, Germany
关键词
RNA-POSITIVE CELLS; BREAST-CANCER; PERIPHERAL-BLOOD; PROGNOSTIC VALUE; MOLECULAR CHARACTERIZATION; ADJUVANT CHEMOTHERAPY; CYTOKERATIN-19; CHALLENGES; FUTURE; HER2;
D O I
10.1021/acs.analchem.8b04975
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Liquid biopsy, based on the molecular information extracted from circulating tumor cells (CTCs) and circulating tumor DNA (ctDNA), offers the possibility to characterize the evolution of a solid tumor in real time and is highly important for diagnostic and therapeutic purposes. The aim of the present study was the development and validation of a novel liquid bead array methodology for the molecular characterization of CTCs and its application in breast cancer. In the present study we developed and evaluated a multiplex polymerase chain reaction (PCR)-coupled liquid bead array (MLBA) assay for studying simultaneously the expression of 14 genes in CTCs. The 14-gene MLBA assay is characterized by high analytical specificity, sensitivity, and reproducibility. The analytical performance of the 14-gene MLBA assay was compared with a commercially available test (AdnaTest Breast Cancer, Qiagen, Germany) and our previously described multiplex quantitative reverse transcription PCR (RT-qPCR) assays. The developed assay has the potential to be further expanded in order to include up to 100 gene targets. The assay is highly specific for each target gene and is not affected by the numerous primers and probes used for multiplexing; hence, it constitutes a sample-, cost-, and time-saving analysis.
引用
收藏
页码:3443 / 3451
页数:9
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