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BAFF and APRIL as TNF superfamily molecules and angiogenesis parallel progression of human multiple myeloma

Tumour necrosis factor alpha (TNF-α) is an inflammatory cytokine with a wide spectrum of biological activity, including angiogenesis. B cell activating factor (BAFF) and a proliferation-inducing ligand (APRIL) are members of the TNF-α family. Vascular endothelial growth factor (VEGF), on the other h...

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Autores principales: Bolkun, L., Lemancewicz, D., Jablonska, E., Kulczynska, A., Bolkun-Skornicka, U., Kloczko, J., Dzieciol, J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3945232/
https://www.ncbi.nlm.nih.gov/pubmed/24141333
http://dx.doi.org/10.1007/s00277-013-1924-9
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author Bolkun, L.
Lemancewicz, D.
Jablonska, E.
Kulczynska, A.
Bolkun-Skornicka, U.
Kloczko, J.
Dzieciol, J.
author_facet Bolkun, L.
Lemancewicz, D.
Jablonska, E.
Kulczynska, A.
Bolkun-Skornicka, U.
Kloczko, J.
Dzieciol, J.
author_sort Bolkun, L.
collection PubMed
description Tumour necrosis factor alpha (TNF-α) is an inflammatory cytokine with a wide spectrum of biological activity, including angiogenesis. B cell activating factor (BAFF) and a proliferation-inducing ligand (APRIL) are members of the TNF-α family. Vascular endothelial growth factor (VEGF), on the other hand, is one of the most characteristic pro-angiogenic cytokines produced by multiple cell types in multiple myeloma (MM). We have analysed BAFF and APRIL concentrations in parallel with pro-angiogenic cytokines in serum and trephine biopsy, and the bone marrow microvascular density (MVD) in 50 patients with newly diagnosed IgG MM and 24 healthy volunteers. The study showed statistically higher concentrations of BAFF, APRIL and TNF-α, as well as VEGF and its receptor, in MM patients compared to healthy volunteers and patients in advanced stages of the disease. A statistically positive correlation between the concentration of TNF-α and the expression of VEGF was demonstrated, and so was a positive link between BAFF, APRIL, MVD and lactate dehydrogenase (LDH). Furthermore, we observed a significant decrease in all studied cytokines after anti-angiogenic therapy, with meaningful differences between responders (at least partial remission) and patients with stable disease. It was also established that APRIL, but not BAFF, correlated with pro-angiogenic cytokines such as VEGF with its receptor, MVD and syndecan-1. Finally, our results showed that serum BAFF and APRIL levels could be useful biomarkers of MM disease activity and its progression which suggests that APRIL could be a possible novel therapeutic target in MM.
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spelling pubmed-39452322014-03-12 BAFF and APRIL as TNF superfamily molecules and angiogenesis parallel progression of human multiple myeloma Bolkun, L. Lemancewicz, D. Jablonska, E. Kulczynska, A. Bolkun-Skornicka, U. Kloczko, J. Dzieciol, J. Ann Hematol Original Article Tumour necrosis factor alpha (TNF-α) is an inflammatory cytokine with a wide spectrum of biological activity, including angiogenesis. B cell activating factor (BAFF) and a proliferation-inducing ligand (APRIL) are members of the TNF-α family. Vascular endothelial growth factor (VEGF), on the other hand, is one of the most characteristic pro-angiogenic cytokines produced by multiple cell types in multiple myeloma (MM). We have analysed BAFF and APRIL concentrations in parallel with pro-angiogenic cytokines in serum and trephine biopsy, and the bone marrow microvascular density (MVD) in 50 patients with newly diagnosed IgG MM and 24 healthy volunteers. The study showed statistically higher concentrations of BAFF, APRIL and TNF-α, as well as VEGF and its receptor, in MM patients compared to healthy volunteers and patients in advanced stages of the disease. A statistically positive correlation between the concentration of TNF-α and the expression of VEGF was demonstrated, and so was a positive link between BAFF, APRIL, MVD and lactate dehydrogenase (LDH). Furthermore, we observed a significant decrease in all studied cytokines after anti-angiogenic therapy, with meaningful differences between responders (at least partial remission) and patients with stable disease. It was also established that APRIL, but not BAFF, correlated with pro-angiogenic cytokines such as VEGF with its receptor, MVD and syndecan-1. Finally, our results showed that serum BAFF and APRIL levels could be useful biomarkers of MM disease activity and its progression which suggests that APRIL could be a possible novel therapeutic target in MM. Springer Berlin Heidelberg 2013-10-19 2014 /pmc/articles/PMC3945232/ /pubmed/24141333 http://dx.doi.org/10.1007/s00277-013-1924-9 Text en © The Author(s) 2013 https://creativecommons.org/licenses/by-nc/2.0/ Open Access This article is distributed under the terms of the Creative Commons Attribution License which permits any use, distribution, and reproduction in any medium, provided the original author(s) and the source are credited.
spellingShingle Original Article
Bolkun, L.
Lemancewicz, D.
Jablonska, E.
Kulczynska, A.
Bolkun-Skornicka, U.
Kloczko, J.
Dzieciol, J.
BAFF and APRIL as TNF superfamily molecules and angiogenesis parallel progression of human multiple myeloma
title BAFF and APRIL as TNF superfamily molecules and angiogenesis parallel progression of human multiple myeloma
title_full BAFF and APRIL as TNF superfamily molecules and angiogenesis parallel progression of human multiple myeloma
title_fullStr BAFF and APRIL as TNF superfamily molecules and angiogenesis parallel progression of human multiple myeloma
title_full_unstemmed BAFF and APRIL as TNF superfamily molecules and angiogenesis parallel progression of human multiple myeloma
title_short BAFF and APRIL as TNF superfamily molecules and angiogenesis parallel progression of human multiple myeloma
title_sort baff and april as tnf superfamily molecules and angiogenesis parallel progression of human multiple myeloma
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3945232/
https://www.ncbi.nlm.nih.gov/pubmed/24141333
http://dx.doi.org/10.1007/s00277-013-1924-9
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