Comparison of two techniques for the screening of human tumor cells in mouse blood: Quantitative real-time polymerase chain reaction (qRT-PCR) versus laser scanning cytometry (LSC).

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Comparison of two techniques for the screening of human tumor cells in mouse blood: Quantitative real-time polymerase chain reaction (qRT-PCR) versus laser scanning cytometry (LSC). / Nehmann, Nina; Wicklein, Daniel; Schumacher, Udo; Müller, Reinhard.

in: ACTA HISTOCHEM, Jahrgang 112, Nr. 5, 2010, S. 489-96.

Publikationen: SCORING: Beitrag in Fachzeitschrift/ZeitungSCORING: ZeitschriftenaufsatzForschungBegutachtung

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@article{fb0552881925496da99f973bac2a20b0,
title = "Comparison of two techniques for the screening of human tumor cells in mouse blood: Quantitative real-time polymerase chain reaction (qRT-PCR) versus laser scanning cytometry (LSC).",
abstract = "The formation of metastases is often investigated in xenografted human tumors in mice and the need arises to detect disseminated human tumor cells in small volumes of mouse blood. Two techniques, namely quantitative real-time polymerase chain reaction (qRT-PCR) and laser scanning cytometry (LSC), were compared for screening of 100mul blood samples from immunodeficient mice spiked with a defined number of human HT29 colon carcinoma cells. With both techniques (qRT-PCR for amplifying of human Alu-sequences and LSC techniques for screening of fluorescence labelled cells), it was possible to detect single disseminated human tumor cells. Using the qRT-PCR technique, a recovery rate of nearly 100% was found when 10-10000 cells were added to 100mul blood. In contrast, the median recovery rate of the LSC technique varied between 20% (10cells/100mul blood) and 7.5% (10000cells/100mul blood). Thus, it is advisable to quantify the number of human tumor cells in mouse blood by qRT-PCR and to use LSC for phenotyping of disseminated tumor cells only.",
author = "Nina Nehmann and Daniel Wicklein and Udo Schumacher and Reinhard M{\"u}ller",
year = "2010",
language = "Deutsch",
volume = "112",
pages = "489--96",
journal = "ACTA HISTOCHEM",
issn = "0065-1281",
publisher = "Urban und Fischer Verlag Jena",
number = "5",

}

RIS

TY - JOUR

T1 - Comparison of two techniques for the screening of human tumor cells in mouse blood: Quantitative real-time polymerase chain reaction (qRT-PCR) versus laser scanning cytometry (LSC).

AU - Nehmann, Nina

AU - Wicklein, Daniel

AU - Schumacher, Udo

AU - Müller, Reinhard

PY - 2010

Y1 - 2010

N2 - The formation of metastases is often investigated in xenografted human tumors in mice and the need arises to detect disseminated human tumor cells in small volumes of mouse blood. Two techniques, namely quantitative real-time polymerase chain reaction (qRT-PCR) and laser scanning cytometry (LSC), were compared for screening of 100mul blood samples from immunodeficient mice spiked with a defined number of human HT29 colon carcinoma cells. With both techniques (qRT-PCR for amplifying of human Alu-sequences and LSC techniques for screening of fluorescence labelled cells), it was possible to detect single disseminated human tumor cells. Using the qRT-PCR technique, a recovery rate of nearly 100% was found when 10-10000 cells were added to 100mul blood. In contrast, the median recovery rate of the LSC technique varied between 20% (10cells/100mul blood) and 7.5% (10000cells/100mul blood). Thus, it is advisable to quantify the number of human tumor cells in mouse blood by qRT-PCR and to use LSC for phenotyping of disseminated tumor cells only.

AB - The formation of metastases is often investigated in xenografted human tumors in mice and the need arises to detect disseminated human tumor cells in small volumes of mouse blood. Two techniques, namely quantitative real-time polymerase chain reaction (qRT-PCR) and laser scanning cytometry (LSC), were compared for screening of 100mul blood samples from immunodeficient mice spiked with a defined number of human HT29 colon carcinoma cells. With both techniques (qRT-PCR for amplifying of human Alu-sequences and LSC techniques for screening of fluorescence labelled cells), it was possible to detect single disseminated human tumor cells. Using the qRT-PCR technique, a recovery rate of nearly 100% was found when 10-10000 cells were added to 100mul blood. In contrast, the median recovery rate of the LSC technique varied between 20% (10cells/100mul blood) and 7.5% (10000cells/100mul blood). Thus, it is advisable to quantify the number of human tumor cells in mouse blood by qRT-PCR and to use LSC for phenotyping of disseminated tumor cells only.

M3 - SCORING: Zeitschriftenaufsatz

VL - 112

SP - 489

EP - 496

JO - ACTA HISTOCHEM

JF - ACTA HISTOCHEM

SN - 0065-1281

IS - 5

ER -