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Identification of the source of elevated hepatocyte growth factor levels in multiple myeloma patients

BACKGROUND: Hepatocyte growth factor (HGF) is a pleiotropic cytokine which can lead to cancer cell proliferation, migration and metastasis. In multiple myeloma (MM) patients it is an abundant component of the bone marrow. HGF levels are elevated in 50% of patients and associated with poor prognosis....

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Autores principales: Rampa, Christoph, Tian, Erming, Våtsveen, Thea Kristin, Buene, Glenn, Slørdahl, Tobias Schmidt, Børset, Magne, Waage, Anders, Sundan, Anders
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4022385/
https://www.ncbi.nlm.nih.gov/pubmed/24716444
http://dx.doi.org/10.1186/2050-7771-2-8
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author Rampa, Christoph
Tian, Erming
Våtsveen, Thea Kristin
Buene, Glenn
Slørdahl, Tobias Schmidt
Børset, Magne
Waage, Anders
Sundan, Anders
author_facet Rampa, Christoph
Tian, Erming
Våtsveen, Thea Kristin
Buene, Glenn
Slørdahl, Tobias Schmidt
Børset, Magne
Waage, Anders
Sundan, Anders
author_sort Rampa, Christoph
collection PubMed
description BACKGROUND: Hepatocyte growth factor (HGF) is a pleiotropic cytokine which can lead to cancer cell proliferation, migration and metastasis. In multiple myeloma (MM) patients it is an abundant component of the bone marrow. HGF levels are elevated in 50% of patients and associated with poor prognosis. Here we aim to investigate its source in myeloma. METHODS: HGF mRNA levels in bone marrow core biopsies from healthy individuals and myeloma patients were quantified by real-time PCR. HGF gene expression profiling in CD138(+) cells isolated from bone marrow aspirates of healthy individuals and MM patients was performed by microarray analysis. HGF protein concentrations present in peripheral blood of MM patients were measured by enzyme-linked immunosorbent assay (ELISA). Cytogenetic status of CD138(+) cells was determined by fluorescence in situ hybridization (FISH) and DNA sequencing of the HGF gene promoter. HGF secretion in co-cultures of human myeloma cell lines and bone marrow stromal cells was measured by ELISA. RESULTS: HGF gene expression profiling in both bone marrow core biopsies and CD138(+) cells showed elevated HGF mRNA levels in myeloma patients. HGF mRNA levels in biopsies and in myeloma cells correlated. Quantification of HGF protein levels in serum also correlated with HGF mRNA levels in CD138(+) cells from corresponding patients. Cytogenetic analysis showed myeloma cell clones with HGF copy numbers between 1 and 3 copies. There was no correlation between HGF copy number and HGF mRNA levels. Co-cultivation of the human myeloma cell lines ANBL-6 and JJN3 with bone marrow stromal cells or the HS-5 cell line resulted in a significant increase in secreted HGF. CONCLUSIONS: We here show that in myeloma patients HGF is primarily produced by malignant plasma cells, and that HGF production by these cells might be supported by the bone marrow microenvironment. Considering the fact that elevated HGF serum and plasma levels predict poor prognosis, these findings are of particular importance for patients harbouring a myeloma clone which produces large amounts of HGF.
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spelling pubmed-40223852014-05-16 Identification of the source of elevated hepatocyte growth factor levels in multiple myeloma patients Rampa, Christoph Tian, Erming Våtsveen, Thea Kristin Buene, Glenn Slørdahl, Tobias Schmidt Børset, Magne Waage, Anders Sundan, Anders Biomark Res Research BACKGROUND: Hepatocyte growth factor (HGF) is a pleiotropic cytokine which can lead to cancer cell proliferation, migration and metastasis. In multiple myeloma (MM) patients it is an abundant component of the bone marrow. HGF levels are elevated in 50% of patients and associated with poor prognosis. Here we aim to investigate its source in myeloma. METHODS: HGF mRNA levels in bone marrow core biopsies from healthy individuals and myeloma patients were quantified by real-time PCR. HGF gene expression profiling in CD138(+) cells isolated from bone marrow aspirates of healthy individuals and MM patients was performed by microarray analysis. HGF protein concentrations present in peripheral blood of MM patients were measured by enzyme-linked immunosorbent assay (ELISA). Cytogenetic status of CD138(+) cells was determined by fluorescence in situ hybridization (FISH) and DNA sequencing of the HGF gene promoter. HGF secretion in co-cultures of human myeloma cell lines and bone marrow stromal cells was measured by ELISA. RESULTS: HGF gene expression profiling in both bone marrow core biopsies and CD138(+) cells showed elevated HGF mRNA levels in myeloma patients. HGF mRNA levels in biopsies and in myeloma cells correlated. Quantification of HGF protein levels in serum also correlated with HGF mRNA levels in CD138(+) cells from corresponding patients. Cytogenetic analysis showed myeloma cell clones with HGF copy numbers between 1 and 3 copies. There was no correlation between HGF copy number and HGF mRNA levels. Co-cultivation of the human myeloma cell lines ANBL-6 and JJN3 with bone marrow stromal cells or the HS-5 cell line resulted in a significant increase in secreted HGF. CONCLUSIONS: We here show that in myeloma patients HGF is primarily produced by malignant plasma cells, and that HGF production by these cells might be supported by the bone marrow microenvironment. Considering the fact that elevated HGF serum and plasma levels predict poor prognosis, these findings are of particular importance for patients harbouring a myeloma clone which produces large amounts of HGF. BioMed Central 2014-04-09 /pmc/articles/PMC4022385/ /pubmed/24716444 http://dx.doi.org/10.1186/2050-7771-2-8 Text en Copyright © 2014 Rampa et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Rampa, Christoph
Tian, Erming
Våtsveen, Thea Kristin
Buene, Glenn
Slørdahl, Tobias Schmidt
Børset, Magne
Waage, Anders
Sundan, Anders
Identification of the source of elevated hepatocyte growth factor levels in multiple myeloma patients
title Identification of the source of elevated hepatocyte growth factor levels in multiple myeloma patients
title_full Identification of the source of elevated hepatocyte growth factor levels in multiple myeloma patients
title_fullStr Identification of the source of elevated hepatocyte growth factor levels in multiple myeloma patients
title_full_unstemmed Identification of the source of elevated hepatocyte growth factor levels in multiple myeloma patients
title_short Identification of the source of elevated hepatocyte growth factor levels in multiple myeloma patients
title_sort identification of the source of elevated hepatocyte growth factor levels in multiple myeloma patients
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4022385/
https://www.ncbi.nlm.nih.gov/pubmed/24716444
http://dx.doi.org/10.1186/2050-7771-2-8
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