Please use this identifier to cite or link to this item: http://hdl.handle.net/2445/104175
Title: Treatment with G-CSF reduces acute myeloid leukemia blast viability in the presence of bone marrow stroma
Author: Nomdedeu i Fàbrega, Meritxell
Lara Castillo, María Carmen
Etxabe, Amaia
Cornet Masana, Josep M.
Pratcorona, Marta
Díaz Beyá, Marina
Calvo, Xavier
Rozman, María
Costa, Dolors
Esteve Reyner, Jordi
Risueño, Ruth M.
Keywords: Leucèmia mieloide
Hematologia
Medul·la òssia
Terapèutica
Factors de creixement
Myeloid leukemia
Hematology
Bone marrow
Therapeutics
Growth factors
Issue Date: 21-Dec-2015
Publisher: BioMed Central
Abstract: BACKGROUND: The resulting clinical impact of the combined use of G-CSF with chemotherapy as a chemosensitizing strategy for treatment of acute myeloid leukemia (AML) patients is still controversial. In this study, the effect of ex vivo treatment with G-CSF on AML primary blasts was studied. METHODS: Peripheral blood mononuclear cells from AML patients were treated with G-CSF at increasing doses, alone or in co-culture with HS-5 stromal cells. Cell viability and surface phenotype was determined by flow cytometry 72 h after treatment. For clonogenicity assays, AML primary samples were treated for 18 h with G-CSF at increasing concentrations and cultured in methyl-cellulose for 14 days. Colonies were counted based on cellularity and morphology criteria. RESULTS: The presence of G-CSF reduced the overall viability of AML cells co-cultured with bone marrow stroma; whereas, in absence of stroma, a negligible effect was observed. Moreover, clonogenic capacity of AML cells was significantly reduced upon treatment with G-CSF. Interestingly, reduction in the AML clonogenic capacity correlated with the sensitivity to chemotherapy observed in vivo. CONCLUSIONS: These ex vivo results would provide a biological basis to data available from studies showing a clinical benefit with the use of G-CSF as a priming agent in patients with a chemosensitive AML and would support implementation of further studies exploring new strategies of chemotherapy priming in AML.
Note: Reproducció del document publicat a: https://doi.org/10.1186/s12935-015-0272-3
It is part of: Cancer Cell International, 2015, vol. 15, p. 122
Related resource: https://doi.org/10.1186/s12935-015-0272-3
URI: http://hdl.handle.net/2445/104175
ISSN: 1475-2867
Appears in Collections:Articles publicats en revistes (Medicina)

Files in This Item:
File Description SizeFormat 
663516.pdf1.01 MBAdobe PDFView/Open


This item is licensed under a Creative Commons License Creative Commons