Novel microgel culture system as semi-solid three-dimensional in vitro model for the study of multiple myeloma proliferation and drug resistance.
Acrylic acid
Drug resistance
Emulsion polymerization
Microgels
Microspheres
Multiple myeloma
Journal
Biomaterials advances
ISSN: 2772-9508
Titre abrégé: Biomater Adv
Pays: Netherlands
ID NLM: 9918383886206676
Informations de publication
Date de publication:
Apr 2022
Apr 2022
Historique:
received:
25
01
2022
revised:
28
02
2022
accepted:
04
03
2022
entrez:
5
8
2022
pubmed:
6
8
2022
medline:
9
8
2022
Statut:
ppublish
Résumé
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.
Identifiants
pubmed: 35929221
pii: S2772-9508(22)00026-7
doi: 10.1016/j.bioadv.2022.212749
pii:
doi:
Substances chimiques
Microgels
0
Bortezomib
69G8BD63PP
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
212749Informations de copyright
Copyright © 2022 The Authors. Published by Elsevier B.V. All rights reserved.