Multimarker Analysis of Circulating Tumor Cells in Peripheral Blood of Metastatic Breast Cancer Patients: A Step Forward in Personalized Medicine

被引:34
作者
de Albuquerque, Andreia [1 ,2 ]
Kaul, Sepp [2 ]
Breier, Georg [1 ]
Krabisch, Petra [3 ]
Fersis, Nikos
机构
[1] Univ Dresden, Fac Med Carl Gustav Carus, Dept Pathol, Dresden, Germany
[2] Zentrum Diagnost, Dept Mol Biol, Chemnitz, Germany
[3] Klinikum Chemnitz, Dept Obstet & Gynaecol, Chemnitz, Germany
关键词
Circulating tumor cells; Metastatic breast cancer; Immunomagnetic separation; Real-time reverse transcription-polymerase chain reaction; Gene expression analysis; RNA-POSITIVE CELLS; EXPRESSION; THERAPY; STRATIFICATION; CHEMOTHERAPY; MANAGEMENT; FUTURE; EPCAM;
D O I
10.1159/000336548
中图分类号
R73 [肿瘤学];
学科分类号
100214 [肿瘤学];
摘要
Aim: To develop an immunomagnetic assay for the isolation of circulating tumor cells (CTCs) followed by the analysis of a multimarker panel, which will enable the characterization of these malignant cells with high accuracy. Patients and Methods: Peripheral blood (PB) was collected from 32 metastatic breast cancer patients and 42 negative controls. The antibodies BM7 and VU1D9 were used for immunomagnetic tumor cell enrichment. A real-time reverse transcription-polymerase chain reaction (RT-PCR) approach for the markers KRT19, SCGB2A2, MUC1, EPCAM, BIRC5 and ERBB2 was used for CTC detection and characterization. Results: The positivity rates for each marker were as follows: 46.9% for KRT19, 25.0% for SCGB2A2, 28.1% for MUC1, 28.1% for EPCAM, 21.9% for BIRC5, and 15.6% for ERBB2. After the creation of individualized cutoffs, the sensitivity and specificity of the combined marker gene panel increased to 56.3% and 100%, respectively. Interestingly, 27.0% of the HER2-negative tumor patients showed ERBB2 mRNA-positive CTCs. Conclusions: The described technique can be used to measure CTCs with great accuracy. The use of a multimarker panel for the characterization of CTCs may provide real-time information and be of great value in therapy monitoring.
引用
收藏
页码:7 / 12
页数:6
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