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Development and Validation of Multiplex Liquid Bead Array Assay for the Simultaneous Expression of 14 Genes in Circulating Tumor Cells.
Parisi, Cleo; Markou, Athina; Strati, Areti; Kasimir-Bauer, Sabine; Lianidou, Evi S.
  • Parisi C; Analysis of Circulating Tumor Cells Lab, Laboratory of Analytical Chemistry, Department of Chemistry , University of Athens , Athens 15771 , Greece.
  • Markou A; Analysis of Circulating Tumor Cells Lab, Laboratory of Analytical Chemistry, Department of Chemistry , University of Athens , Athens 15771 , Greece.
  • Strati A; Analysis of Circulating Tumor Cells Lab, Laboratory of Analytical Chemistry, Department of Chemistry , University of Athens , Athens 15771 , Greece.
  • Kasimir-Bauer S; Department of Gynecology and Obstetrics , University Hospital of Essen, University of Duisburg-Essen , D-45122 Essen , Germany.
  • Lianidou ES; Analysis of Circulating Tumor Cells Lab, Laboratory of Analytical Chemistry, Department of Chemistry , University of Athens , Athens 15771 , Greece.
Anal Chem ; 91(5): 3443-3451, 2019 03 05.
Article en En | MEDLINE | ID: mdl-30663875
ABSTRACT
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 BreastCancer, 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.
Asunto(s)

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: ADN de Neoplasias / Biomarcadores de Tumor / Análisis de Secuencia por Matrices de Oligonucleótidos / Reacción en Cadena de la Polimerasa Multiplex / Células Neoplásicas Circulantes Límite: Humans Idioma: En Año: 2019 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: ADN de Neoplasias / Biomarcadores de Tumor / Análisis de Secuencia por Matrices de Oligonucleótidos / Reacción en Cadena de la Polimerasa Multiplex / Células Neoplásicas Circulantes Límite: Humans Idioma: En Año: 2019 Tipo del documento: Article