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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....
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2014
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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. |
format | Online Article Text |
id | pubmed-4022385 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
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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