Detection of tumor cells in peripheral blood samples from patients with germ cell tumors using immunocytochemical and reverse transcriptase-polymerase chain reaction techniques
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作者:
MO Hildebrandt
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机构:Blood Bank,Department of Hematology and Oncology
MO Hildebrandt
F Bläser
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机构:Blood Bank,Department of Hematology and Oncology
F Bläser
J Beyer
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机构:Blood Bank,Department of Hematology and Oncology
J Beyer
W Siegert
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机构:Blood Bank,Department of Hematology and Oncology
W Siegert
MY Mapara
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机构:Blood Bank,Department of Hematology and Oncology
MY Mapara
D Huhn
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机构:Blood Bank,Department of Hematology and Oncology
D Huhn
A Salama
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机构:Blood Bank,Department of Hematology and Oncology
A Salama
机构:
[1] Blood Bank,Department of Hematology and Oncology
[2] Charité Campus Virchow-Klinikum,Department of Hematology
[3] Humboldt University,undefined
[4] Oncology and Tumor Immunology,undefined
[5] Robert Rössle-Klinik at the Max Delbrück Centrum for Molecular Medicine,undefined
The aim of this study was to establish sensitive techniques for the detection of residual germ cell tumor cells in peripheral blood and progenitor cell harvests. For this purpose, we used immunocytochemical staining for cytokeratin filaments and reverse transcriptase- polymerase chain reaction (RT-PCR) for epidermal growth factor receptor (EGF-R) and germ cell alkaline phosphatase (GCAP). Germ cell tumor lines Tera-1 and Tera-2 were titrated into normal peripheral blood. Immunocytochemical staining allowed detection of one cytokeratin-positive tumor cell in 105 cells. RT-PCR for EGF-R revealed one tumor cell in 10 cells for Tera-1 and one tumor cell in 103 cells for Tera-2, while RT-PCR for GCAP displayed a sensitivity of one tumor cell in 106 cells for Tera-1, one tumor cell in 104 cells for Tera-2, and no positivity in normal mononuclear cells (n = 20) and progenitor cell harvests (n = 5). The analysis of peripheral blood and progenitor cell harvests from 20 patients with germ cell tumors revealed tumor cell contamination in three patients using immunocytochemical staining and in seven patients by RT-PCR for GCAP. We conclude that RT-PCR for GCAP appears to be suitable for the sensitive detection of residual germ cell tumor cells in peripheral blood and progenitor cell harvests.