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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...
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/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. |
format | Online Article Text |
id | pubmed-8145732 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT leowchristopherchangyew targetedtherapiesformultiplemyeloma AT lowmichaelszeyuan targetedtherapiesformultiplemyeloma |