Novel microgel culture system as semi-solid three-dimensional in vitro model for the study of multiple myeloma proliferation and drug resistance
Fecha
Autores
Clara Trujillo, Sandra
Tolosa, Laia
Cordón, Lourdes
Sempere, Amparo
Gallego Ferrer, Gloria
Gómez Ribelles, José Luís
Directores
Unidades organizativas
Handle
https://riunet.upv.es/handle/10251/197775
Cita bibliográfica
Clara-Trujillo, S.; Tolosa, L.; Cordón, L.; Sempere, A.; Gallego-Ferrer, G.; Gómez Ribelles, JL. (2022). Novel microgel culture system as semi-solid three-dimensional in vitro model for the study of multiple myeloma proliferation and drug resistance. Biomaterials Advances. 135:1-13. https://doi.org/10.1016/j.bioadv.2022.212749
Titulación
Resumen
[EN] Multiple myeloma (MM) is a hematological malignancy in which the patient's drug resistance is one of the main clinical problems. As 2D cultures do not recapitulate the cellular microenvironment, which has a key role in drug resistance, there is an urgent need for better biomimetic models. Here, a novel 3D platform is used to model MM. The semi-solid culture consists of a dynamic suspension of microspheres and MM cells, termed as microgel. Microspheres are synthesized with acrylic polymers of different sizes, compositions, and functionalities (fibronectin or hyaluronic acid). Optimal conditions for the platform in terms of agitation speed and microsphere size have been determined. With these parameters the system allows good proliferation of the MM cell lines RPMI8226, U226, and MM1.S. Interestingly, when used for drug resistance studies, culture of the three MM cell lines in microgels showed close agreement in revealing the role of acrylic acid in resistance to anti-MM drugs such as dexamethasone and bortezomib. This work presents a unique platform for the in vitro modeling of non-solid tumors since it allows keeping non-adherent cells in suspension conditions but in a 3D context that can be easily tuned with different functionalizations.
Palabras clave
Multiple myeloma, Microgels, Microspheres, Emulsion polymerization, Drug resistance, Acrylic acid
ISSN
ISBN
Fuente
Biomaterials Advances
DOI
10.1016/j.bioadv.2022.212749
Versión del editor
https://doi.org/10.1016/j.bioadv.2022.212749
dc.description.uri
Código de Proyecto
info:eu-repo/grantAgreement/AEI/Plan Estatal de Investigación Científica y Técnica y de Innovación 2017-2020/PID2019-106099RB-C41/ES/MICROGELES BIOMIMETICOS PARA EL ESTUDIO DE LA GENERACION DE RESISTENCIAS A FARMACOS EN EL MIELOMA MULTIPLE/
info:eu-repo/grantAgreement/MIU//FPU17%2F05810/ES/PERSONALIZED MEDICINE DEVICES FOR BLOOD CANCERS/
info:eu-repo/grantAgreement/MIU//FPU17%2F05810/ES/PERSONALIZED MEDICINE DEVICES FOR BLOOD CANCERS/
Agradecimientos
This work was funded by the Spanish State Research Agency (AEI) through the PID2019-106099RB-C41/AEI/10.13039/501100011033 Project. CIBER-BBN is an initiative funded by the VI National R&D&I Plan 2008-2011, Iniciativa Ingenio 2010, Consolider Program. CIBER Actions were financed by the Instituto de Salud Carlos III with assistance from the European Regional Development Fund. This work was also supported by the Spanish Ministry of Science, Innovation and Universities through Grant NO FPU17/05810 awarded to Sandra Clara-Trujillo. The Microscopy Service of the UPV (UniversitatPolitecnica de València) is gratefully acknowledged for helping with FESEM characterization.