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• W2186192588 endingPage "159" @default.
• W2186192588 startingPage "150" @default.
• W2186192588 abstract "Recombinant human erythropoietin (Epo) and granulocyte-colony-stimulating factor (G-CSF) are used to stimulate hematopoiesis in patients with malignant diseases. These cytokines transduce their biological signal via the Epo receptor (EpoR) and G-CSF receptor (G-CSF-R) into the cell. We therefore investigated in human tumor cell lines the expression of these receptors in tumor cells as well as their response to Epo and G-CSF.The expression of EpoR and G-CSF-R mRNA was analyzed with reverse transcription-polymerase chain reaction (RT-PCR). EpoR protein expression was further monitored with Western blot and immunocytochemistry analysis. The cellular response to various concentrations of Epo was evaluated using 3[H]-thymidine uptake, Northern blot of c-fos expression and tyrosine kinase activity assay. The proliferation after G-CSF incubation was analyzed with the MTS assay.In this study EpoR mRNA and protein were detected in various human tumor cell lines. Treatment with Epo did not influence the proliferation rate of examined EpoR-positive tumor cell lines. Epo did not stimulate the tyrosine kinase activity nor did it affect the c-fos mRNA in these cell lines. G-CSF-R mRNA was only detected in two myeloid cell lines. Treatment with G-CSF did not increase the proliferation of these cells.These results demonstrate that Epo and G-CSF did not modulate the growth rate of examined receptor-positive tumor cell lines; the presence of the Epo receptor seems not essential for cell growth of these tumor cells in cell culture." @default.
• W2186192588 created "2016-06-24" @default.
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• W2186192588 date "2002-03-01" @default.
• W2186192588 modified "2023-09-25" @default.
• W2186192588 title "Erythropoietin and G-csf Receptors in Human Tumor Cells: Expression and Aspects regarding Functionality" @default.
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• W2186192588 doi "https://doi.org/10.1177/030089160208800214" @default.
• W2186192588 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/12088257" @default.
• W2186192588 hasPublicationYear "2002" @default.
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