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Prognostic Value of Resistance Proteins in Plasma Cells from Multiple Myeloma Patients Treated with Bortezomib-Based Regimens
While multiple myeloma (MM) treatment with proteasome inhibitors and other agents yields encouraging results, primary and secondary resistance remains an emerging problem. An important factor in such treatment resistance is the overexpression of several proteins. The present study comprehensively ev...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8584776/ https://www.ncbi.nlm.nih.gov/pubmed/34768548 http://dx.doi.org/10.3390/jcm10215028 |
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author | Robak, Paweł Szemraj, Janusz Mikulski, Damian Drozdz, Izabela Juszczak, Karolina Jarych, Dariusz Misiewicz, Małgorzata Kościelny, Kacper Fendler, Wojciech Robak, Tadeusz |
author_facet | Robak, Paweł Szemraj, Janusz Mikulski, Damian Drozdz, Izabela Juszczak, Karolina Jarych, Dariusz Misiewicz, Małgorzata Kościelny, Kacper Fendler, Wojciech Robak, Tadeusz |
author_sort | Robak, Paweł |
collection | PubMed |
description | While multiple myeloma (MM) treatment with proteasome inhibitors and other agents yields encouraging results, primary and secondary resistance remains an emerging problem. An important factor in such treatment resistance is the overexpression of several proteins. The present study comprehensively evaluates the expression of POMP, PSMB5, NRF2, XBP1, cMAF and MAFb proteins in plasma cells isolated from the bone marrow of 39 MM patients treated with bortezomib-based regimens using an enzyme-linked immunosorbent assay (ELISA). The proteins were selected on the basis of previous laboratory and clinical studies in bortezomib-treated MM patients. It was found that the expression of the investigated proteins did not significantly differ between bortezomib-sensitive and bortezomib-refractory patients. However, the expression of some proteins correlated with overall survival (OS); this was significantly shorter in patients with higher POMP expression (HR 2.8, 95% CI: 1.1–7.0, p = 0.0277) and longer in those with higher MAFB expression (HR 0.32, 95% CI: 0.13–0.80, p = 0.0147). Our results indicate that a high expression of POMP and MAFB in MM plasma cells may serve as predictors of OS in MM patients treated with bortezomib-based regimens. However, further studies are needed to determine the role of these factors in effective strategies for improving anti-myeloma therapy. |
format | Online Article Text |
id | pubmed-8584776 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-85847762021-11-12 Prognostic Value of Resistance Proteins in Plasma Cells from Multiple Myeloma Patients Treated with Bortezomib-Based Regimens Robak, Paweł Szemraj, Janusz Mikulski, Damian Drozdz, Izabela Juszczak, Karolina Jarych, Dariusz Misiewicz, Małgorzata Kościelny, Kacper Fendler, Wojciech Robak, Tadeusz J Clin Med Article While multiple myeloma (MM) treatment with proteasome inhibitors and other agents yields encouraging results, primary and secondary resistance remains an emerging problem. An important factor in such treatment resistance is the overexpression of several proteins. The present study comprehensively evaluates the expression of POMP, PSMB5, NRF2, XBP1, cMAF and MAFb proteins in plasma cells isolated from the bone marrow of 39 MM patients treated with bortezomib-based regimens using an enzyme-linked immunosorbent assay (ELISA). The proteins were selected on the basis of previous laboratory and clinical studies in bortezomib-treated MM patients. It was found that the expression of the investigated proteins did not significantly differ between bortezomib-sensitive and bortezomib-refractory patients. However, the expression of some proteins correlated with overall survival (OS); this was significantly shorter in patients with higher POMP expression (HR 2.8, 95% CI: 1.1–7.0, p = 0.0277) and longer in those with higher MAFB expression (HR 0.32, 95% CI: 0.13–0.80, p = 0.0147). Our results indicate that a high expression of POMP and MAFB in MM plasma cells may serve as predictors of OS in MM patients treated with bortezomib-based regimens. However, further studies are needed to determine the role of these factors in effective strategies for improving anti-myeloma therapy. MDPI 2021-10-28 /pmc/articles/PMC8584776/ /pubmed/34768548 http://dx.doi.org/10.3390/jcm10215028 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/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 (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Robak, Paweł Szemraj, Janusz Mikulski, Damian Drozdz, Izabela Juszczak, Karolina Jarych, Dariusz Misiewicz, Małgorzata Kościelny, Kacper Fendler, Wojciech Robak, Tadeusz Prognostic Value of Resistance Proteins in Plasma Cells from Multiple Myeloma Patients Treated with Bortezomib-Based Regimens |
title | Prognostic Value of Resistance Proteins in Plasma Cells from Multiple Myeloma Patients Treated with Bortezomib-Based Regimens |
title_full | Prognostic Value of Resistance Proteins in Plasma Cells from Multiple Myeloma Patients Treated with Bortezomib-Based Regimens |
title_fullStr | Prognostic Value of Resistance Proteins in Plasma Cells from Multiple Myeloma Patients Treated with Bortezomib-Based Regimens |
title_full_unstemmed | Prognostic Value of Resistance Proteins in Plasma Cells from Multiple Myeloma Patients Treated with Bortezomib-Based Regimens |
title_short | Prognostic Value of Resistance Proteins in Plasma Cells from Multiple Myeloma Patients Treated with Bortezomib-Based Regimens |
title_sort | prognostic value of resistance proteins in plasma cells from multiple myeloma patients treated with bortezomib-based regimens |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8584776/ https://www.ncbi.nlm.nih.gov/pubmed/34768548 http://dx.doi.org/10.3390/jcm10215028 |
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