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CIK Cells and HDAC Inhibitors in Multiple Myeloma

Multiple myeloma is the second most common hematological malignancy. Despite all the progress made in treating multiple myeloma, it still remains an incurable disease. Patients are left with a median survival of 4–5 years. The combined treatment of multiple myeloma with histone deacetylase inhibitor...

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Detalles Bibliográficos
Autores principales: Stephan, David, Weiher, Hans, Schmidt-Wolf, Ingo G.H.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5454858/
https://www.ncbi.nlm.nih.gov/pubmed/28468247
http://dx.doi.org/10.3390/ijms18050945
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author Stephan, David
Weiher, Hans
Schmidt-Wolf, Ingo G.H.
author_facet Stephan, David
Weiher, Hans
Schmidt-Wolf, Ingo G.H.
author_sort Stephan, David
collection PubMed
description Multiple myeloma is the second most common hematological malignancy. Despite all the progress made in treating multiple myeloma, it still remains an incurable disease. Patients are left with a median survival of 4–5 years. The combined treatment of multiple myeloma with histone deacetylase inhibitors and cytokine-induced killer cells provides a promising targeted treatment option for patients. This study investigated the impact of a combined treatment compared to treatment with histone deacetylase inhibitors. The experiments revealed that a treatment with histone deacetylase (HDAC) inhibitors could reduce cell viability to 59% for KMS 18 cell line and 46% for the U-266 cell line. The combined treatment led to a decrease of cell viability to 33% for KMS 18 and 27% for the U-266 cell line, thus showing a significantly better efficacy than the single treatment.
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spelling pubmed-54548582017-06-08 CIK Cells and HDAC Inhibitors in Multiple Myeloma Stephan, David Weiher, Hans Schmidt-Wolf, Ingo G.H. Int J Mol Sci Article Multiple myeloma is the second most common hematological malignancy. Despite all the progress made in treating multiple myeloma, it still remains an incurable disease. Patients are left with a median survival of 4–5 years. The combined treatment of multiple myeloma with histone deacetylase inhibitors and cytokine-induced killer cells provides a promising targeted treatment option for patients. This study investigated the impact of a combined treatment compared to treatment with histone deacetylase inhibitors. The experiments revealed that a treatment with histone deacetylase (HDAC) inhibitors could reduce cell viability to 59% for KMS 18 cell line and 46% for the U-266 cell line. The combined treatment led to a decrease of cell viability to 33% for KMS 18 and 27% for the U-266 cell line, thus showing a significantly better efficacy than the single treatment. MDPI 2017-04-29 /pmc/articles/PMC5454858/ /pubmed/28468247 http://dx.doi.org/10.3390/ijms18050945 Text en © 2017 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Stephan, David
Weiher, Hans
Schmidt-Wolf, Ingo G.H.
CIK Cells and HDAC Inhibitors in Multiple Myeloma
title CIK Cells and HDAC Inhibitors in Multiple Myeloma
title_full CIK Cells and HDAC Inhibitors in Multiple Myeloma
title_fullStr CIK Cells and HDAC Inhibitors in Multiple Myeloma
title_full_unstemmed CIK Cells and HDAC Inhibitors in Multiple Myeloma
title_short CIK Cells and HDAC Inhibitors in Multiple Myeloma
title_sort cik cells and hdac inhibitors in multiple myeloma
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5454858/
https://www.ncbi.nlm.nih.gov/pubmed/28468247
http://dx.doi.org/10.3390/ijms18050945
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