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Targeted Therapies for Multiple Myeloma

Multiple myeloma continues to be a challenging disorder to treat despite improved therapies and the widespread use of proteasome inhibitors and immunomodulatory drugs. Although patient outcomes have improved, the disease continues to invariably relapse, and in the majority of cases, a cure remains e...

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Autores principales: Leow, Christopher Chang-Yew, Low, Michael Sze Yuan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8145732/
https://www.ncbi.nlm.nih.gov/pubmed/33922567
http://dx.doi.org/10.3390/jpm11050334
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author Leow, Christopher Chang-Yew
Low, Michael Sze Yuan
author_facet Leow, Christopher Chang-Yew
Low, Michael Sze Yuan
author_sort Leow, Christopher Chang-Yew
collection PubMed
description Multiple myeloma continues to be a challenging disorder to treat despite improved therapies and the widespread use of proteasome inhibitors and immunomodulatory drugs. Although patient outcomes have improved, the disease continues to invariably relapse, and in the majority of cases, a cure remains elusive. In the last decade, there has been an explosion of novel drugs targeting cellular proteins essential for malignant plasma cell proliferation and survival. In this review, we focus on novel druggable targets leading to the development of monoclonal antibodies and cellular therapies against surface antigens (CD38, CD47, CD138, BCMA, SLAMF7, GPRC5D, FcRH5), inhibitors of epigenetic regulators such as histone deacetylase (HDAC), and agents targeting anti-apoptotic (BCL-2), ribosomal (eEF1A2) and nuclear export (XPO1) proteins.
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spelling pubmed-81457322021-05-26 Targeted Therapies for Multiple Myeloma Leow, Christopher Chang-Yew Low, Michael Sze Yuan J Pers Med Review Multiple myeloma continues to be a challenging disorder to treat despite improved therapies and the widespread use of proteasome inhibitors and immunomodulatory drugs. Although patient outcomes have improved, the disease continues to invariably relapse, and in the majority of cases, a cure remains elusive. In the last decade, there has been an explosion of novel drugs targeting cellular proteins essential for malignant plasma cell proliferation and survival. In this review, we focus on novel druggable targets leading to the development of monoclonal antibodies and cellular therapies against surface antigens (CD38, CD47, CD138, BCMA, SLAMF7, GPRC5D, FcRH5), inhibitors of epigenetic regulators such as histone deacetylase (HDAC), and agents targeting anti-apoptotic (BCL-2), ribosomal (eEF1A2) and nuclear export (XPO1) proteins. MDPI 2021-04-23 /pmc/articles/PMC8145732/ /pubmed/33922567 http://dx.doi.org/10.3390/jpm11050334 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 Review
Leow, Christopher Chang-Yew
Low, Michael Sze Yuan
Targeted Therapies for Multiple Myeloma
title Targeted Therapies for Multiple Myeloma
title_full Targeted Therapies for Multiple Myeloma
title_fullStr Targeted Therapies for Multiple Myeloma
title_full_unstemmed Targeted Therapies for Multiple Myeloma
title_short Targeted Therapies for Multiple Myeloma
title_sort targeted therapies for multiple myeloma
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8145732/
https://www.ncbi.nlm.nih.gov/pubmed/33922567
http://dx.doi.org/10.3390/jpm11050334
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