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Effects of granulocyte-colony stimulating factor and the expression of its receptor on various malignant cells
BACKGROUND: Granulocyte-colony stimulating factor (G-CSF) is extensively used to improve neutrophil count during anti-cancer chemotherapy. We investigated the effects of G-CSF on several leukemic cell lines and screened for the expression of the G-CSF receptor (G-CSFR) in various malignant cells. ME...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Korean Society of Hematology; Korean Society of Blood and Marrow Transplantation; Korean Society of Pediatric Hematology-Oncology; Korean Society on Thrombosis and Hemostasis
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3464340/ https://www.ncbi.nlm.nih.gov/pubmed/23071478 http://dx.doi.org/10.5045/kjh.2012.47.3.219 |
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author | Moon, Hee Won Kim, Tae Young Oh, Bo Ra Hwang, Sang Mee Kwon, Jiseok Ku, Ja-Lok Lee, Dong Soon |
author_facet | Moon, Hee Won Kim, Tae Young Oh, Bo Ra Hwang, Sang Mee Kwon, Jiseok Ku, Ja-Lok Lee, Dong Soon |
author_sort | Moon, Hee Won |
collection | PubMed |
description | BACKGROUND: Granulocyte-colony stimulating factor (G-CSF) is extensively used to improve neutrophil count during anti-cancer chemotherapy. We investigated the effects of G-CSF on several leukemic cell lines and screened for the expression of the G-CSF receptor (G-CSFR) in various malignant cells. METHODS: We examined the effects of the most commonly used commercial forms of G-CSF (glycosylated lenograstim and nonglycosylated filgrastim) on various leukemic cell lines by flow cytometry. Moreover, we screened for the expression of G-CSFR mRNA in 38 solid tumor cell lines by using real-time PCR. RESULTS: G-CSF stimulated proliferation (40-80% increase in proliferation in treated cells as compared to that in control cells) in 3 leukemic cell lines and induced differentiation of AML1/ETO+ leukemic cells. Among the 38 solid tumor cell lines, 5 cell lines (hepatoblastoma, 2 breast carcinoma, squamous cell carcinoma of the larynx, and melanoma cell lines) showed G-CSFR mRNA expression. CONCLUSION: The results of the present study show that therapeutic G-CSF might stimulate the proliferation and differentiation of malignant cells with G-CSFR expression, suggesting that prescreening for G-CSFR expression in primary tumor cells may be necessary before using G-CSF for treatment. |
format | Online Article Text |
id | pubmed-3464340 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Korean Society of Hematology; Korean Society of Blood and Marrow Transplantation; Korean Society of Pediatric Hematology-Oncology; Korean Society on Thrombosis and Hemostasis |
record_format | MEDLINE/PubMed |
spelling | pubmed-34643402012-10-15 Effects of granulocyte-colony stimulating factor and the expression of its receptor on various malignant cells Moon, Hee Won Kim, Tae Young Oh, Bo Ra Hwang, Sang Mee Kwon, Jiseok Ku, Ja-Lok Lee, Dong Soon Korean J Hematol Original Article BACKGROUND: Granulocyte-colony stimulating factor (G-CSF) is extensively used to improve neutrophil count during anti-cancer chemotherapy. We investigated the effects of G-CSF on several leukemic cell lines and screened for the expression of the G-CSF receptor (G-CSFR) in various malignant cells. METHODS: We examined the effects of the most commonly used commercial forms of G-CSF (glycosylated lenograstim and nonglycosylated filgrastim) on various leukemic cell lines by flow cytometry. Moreover, we screened for the expression of G-CSFR mRNA in 38 solid tumor cell lines by using real-time PCR. RESULTS: G-CSF stimulated proliferation (40-80% increase in proliferation in treated cells as compared to that in control cells) in 3 leukemic cell lines and induced differentiation of AML1/ETO+ leukemic cells. Among the 38 solid tumor cell lines, 5 cell lines (hepatoblastoma, 2 breast carcinoma, squamous cell carcinoma of the larynx, and melanoma cell lines) showed G-CSFR mRNA expression. CONCLUSION: The results of the present study show that therapeutic G-CSF might stimulate the proliferation and differentiation of malignant cells with G-CSFR expression, suggesting that prescreening for G-CSFR expression in primary tumor cells may be necessary before using G-CSF for treatment. Korean Society of Hematology; Korean Society of Blood and Marrow Transplantation; Korean Society of Pediatric Hematology-Oncology; Korean Society on Thrombosis and Hemostasis 2012-09 2012-09-25 /pmc/articles/PMC3464340/ /pubmed/23071478 http://dx.doi.org/10.5045/kjh.2012.47.3.219 Text en © 2012 Korean Society of Hematology http://creativecommons.org/licenses/by-nc/3.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Moon, Hee Won Kim, Tae Young Oh, Bo Ra Hwang, Sang Mee Kwon, Jiseok Ku, Ja-Lok Lee, Dong Soon Effects of granulocyte-colony stimulating factor and the expression of its receptor on various malignant cells |
title | Effects of granulocyte-colony stimulating factor and the expression of its receptor on various malignant cells |
title_full | Effects of granulocyte-colony stimulating factor and the expression of its receptor on various malignant cells |
title_fullStr | Effects of granulocyte-colony stimulating factor and the expression of its receptor on various malignant cells |
title_full_unstemmed | Effects of granulocyte-colony stimulating factor and the expression of its receptor on various malignant cells |
title_short | Effects of granulocyte-colony stimulating factor and the expression of its receptor on various malignant cells |
title_sort | effects of granulocyte-colony stimulating factor and the expression of its receptor on various malignant cells |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3464340/ https://www.ncbi.nlm.nih.gov/pubmed/23071478 http://dx.doi.org/10.5045/kjh.2012.47.3.219 |
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