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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...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
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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. |
format | Online Article Text |
id | pubmed-9657251 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
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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