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Patient-Derived Multiple Myeloma 3D Models for Personalized Medicine—Are We There Yet?

Despite the wide variety of existing therapies, multiple myeloma (MM) remains a disease with dismal prognosis. Choosing the right treatment for each patient remains one of the major challenges. A new approach being explored is the use of ex vivo models for personalized medicine. Two-dimensional cult...

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Autores principales: Lourenço, Diana, Lopes, Raquel, Pestana, Carolina, Queirós, Ana C., João, Cristina, Carneiro, Emilie Arnault
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9657251/
https://www.ncbi.nlm.nih.gov/pubmed/36361677
http://dx.doi.org/10.3390/ijms232112888
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author Lourenço, Diana
Lopes, Raquel
Pestana, Carolina
Queirós, Ana C.
João, Cristina
Carneiro, Emilie Arnault
author_facet Lourenço, Diana
Lopes, Raquel
Pestana, Carolina
Queirós, Ana C.
João, Cristina
Carneiro, Emilie Arnault
author_sort Lourenço, Diana
collection PubMed
description Despite the wide variety of existing therapies, multiple myeloma (MM) remains a disease with dismal prognosis. Choosing the right treatment for each patient remains one of the major challenges. A new approach being explored is the use of ex vivo models for personalized medicine. Two-dimensional culture or animal models often fail to predict clinical outcomes. Three-dimensional ex vivo models using patients’ bone marrow (BM) cells may better reproduce the complexity and heterogeneity of the BM microenvironment. Here, we review the strengths and limitations of currently existing patient-derived ex vivo three-dimensional MM models. We analyze their biochemical and biophysical properties, molecular and cellular characteristics, as well as their potential for drug testing and identification of disease biomarkers. Furthermore, we discuss the remaining challenges and give some insight on how to achieve a more biomimetic and accurate MM BM model. Overall, there is still a need for standardized culture methods and refined readout techniques. Including both myeloma and other cells of the BM microenvironment in a simple and reproducible three-dimensional scaffold is the key to faithfully mapping and examining the relationship between these players in MM. This will allow a patient-personalized profile, providing a powerful tool for clinical and research applications.
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spelling pubmed-96572512022-11-15 Patient-Derived Multiple Myeloma 3D Models for Personalized Medicine—Are We There Yet? Lourenço, Diana Lopes, Raquel Pestana, Carolina Queirós, Ana C. João, Cristina Carneiro, Emilie Arnault Int J Mol Sci Review Despite the wide variety of existing therapies, multiple myeloma (MM) remains a disease with dismal prognosis. Choosing the right treatment for each patient remains one of the major challenges. A new approach being explored is the use of ex vivo models for personalized medicine. Two-dimensional culture or animal models often fail to predict clinical outcomes. Three-dimensional ex vivo models using patients’ bone marrow (BM) cells may better reproduce the complexity and heterogeneity of the BM microenvironment. Here, we review the strengths and limitations of currently existing patient-derived ex vivo three-dimensional MM models. We analyze their biochemical and biophysical properties, molecular and cellular characteristics, as well as their potential for drug testing and identification of disease biomarkers. Furthermore, we discuss the remaining challenges and give some insight on how to achieve a more biomimetic and accurate MM BM model. Overall, there is still a need for standardized culture methods and refined readout techniques. Including both myeloma and other cells of the BM microenvironment in a simple and reproducible three-dimensional scaffold is the key to faithfully mapping and examining the relationship between these players in MM. This will allow a patient-personalized profile, providing a powerful tool for clinical and research applications. MDPI 2022-10-25 /pmc/articles/PMC9657251/ /pubmed/36361677 http://dx.doi.org/10.3390/ijms232112888 Text en © 2022 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
Lourenço, Diana
Lopes, Raquel
Pestana, Carolina
Queirós, Ana C.
João, Cristina
Carneiro, Emilie Arnault
Patient-Derived Multiple Myeloma 3D Models for Personalized Medicine—Are We There Yet?
title Patient-Derived Multiple Myeloma 3D Models for Personalized Medicine—Are We There Yet?
title_full Patient-Derived Multiple Myeloma 3D Models for Personalized Medicine—Are We There Yet?
title_fullStr Patient-Derived Multiple Myeloma 3D Models for Personalized Medicine—Are We There Yet?
title_full_unstemmed Patient-Derived Multiple Myeloma 3D Models for Personalized Medicine—Are We There Yet?
title_short Patient-Derived Multiple Myeloma 3D Models for Personalized Medicine—Are We There Yet?
title_sort patient-derived multiple myeloma 3d models for personalized medicine—are we there yet?
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9657251/
https://www.ncbi.nlm.nih.gov/pubmed/36361677
http://dx.doi.org/10.3390/ijms232112888
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